Influence of Mabs on PrPSc Formation Using In Vitro and Cell-Free Systems
Identifieur interne : 000A15 ( Pmc/Corpus ); précédent : 000A14; suivant : 000A16Influence of Mabs on PrPSc Formation Using In Vitro and Cell-Free Systems
Auteurs : Binggong Chang ; Robert Petersen ; Thomas Wisniewski ; Richard RubensteinSource :
- PLoS ONE [ 1932-6203 ] ; 2012.
Abstract
PrPSc is believed to serve as a template for the conversion of PrPC to the abnormal isoform. This process requires contact between the two proteins and implies that there may be critical contact sites that are important for conversion. We hypothesized that antibodies binding to either PrPcor PrPSc would hinder or prevent the formation of the PrPC–PrPSc complex and thus slow down or prevent the conversion process. Two systems were used to analyze the effect of different antibodies on PrPSc formation: (i) neuroblastoma cells persistently infected with the 22L mouse-adapted scrapie stain, and (ii) protein misfolding cyclic amplification (PMCA), which uses PrPSc as a template or seed, and a series of incubations and sonications, to convert PrPC to PrPSc. The two systems yielded similar results, in most cases, and demonstrate that PrP-specific monoclonal antibodies (Mabs) vary in their ability to inhibit the PrPC–PrPSc conversion process. Based on the numerous and varied Mabs analyzed, the inhibitory effect does not appear to be epitope specific, related to PrPC conformation, or to cell membrane localization, but is influenced by the targeted PrP region (amino vs carboxy).
Url:
DOI: 10.1371/journal.pone.0041626
PubMed: 22848548
PubMed Central: 3407222
Links to Exploration step
PMC:3407222Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Influence of Mabs on PrP<sup>Sc</sup> Formation Using <italic>In Vitro</italic> and Cell-Free Systems</title><author><name sortKey="Chang, Binggong" sort="Chang, Binggong" uniqKey="Chang B" first="Binggong" last="Chang">Binggong Chang</name><affiliation><nlm:aff id="aff1"><addr-line>Departments of Neurology and Physiology/Pharmacology, State University New York Downstate Medical Center, Brooklyn, New York, United States of America</addr-line></nlm:aff></affiliation></author><author><name sortKey="Petersen, Robert" sort="Petersen, Robert" uniqKey="Petersen R" first="Robert" last="Petersen">Robert Petersen</name><affiliation><nlm:aff id="aff2"><addr-line>Departments of Pathology, Neuroscience, and Neurology, Case Western Reserve University, Cleveland, Ohio, United States of America</addr-line></nlm:aff></affiliation></author><author><name sortKey="Wisniewski, Thomas" sort="Wisniewski, Thomas" uniqKey="Wisniewski T" first="Thomas" last="Wisniewski">Thomas Wisniewski</name><affiliation><nlm:aff id="aff3"><addr-line>Departments of Neurology, Psychiatry and Pathology, New York University School of Medicine, New York, New York, United States of America</addr-line></nlm:aff></affiliation></author><author><name sortKey="Rubenstein, Richard" sort="Rubenstein, Richard" uniqKey="Rubenstein R" first="Richard" last="Rubenstein">Richard Rubenstein</name><affiliation><nlm:aff id="aff1"><addr-line>Departments of Neurology and Physiology/Pharmacology, State University New York Downstate Medical Center, Brooklyn, New York, United States of America</addr-line></nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">22848548</idno><idno type="pmc">3407222</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3407222</idno><idno type="RBID">PMC:3407222</idno><idno type="doi">10.1371/journal.pone.0041626</idno><date when="2012">2012</date><idno type="wicri:Area/Pmc/Corpus">000A15</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">000A15</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Influence of Mabs on PrP<sup>Sc</sup> Formation Using <italic>In Vitro</italic> and Cell-Free Systems</title><author><name sortKey="Chang, Binggong" sort="Chang, Binggong" uniqKey="Chang B" first="Binggong" last="Chang">Binggong Chang</name><affiliation><nlm:aff id="aff1"><addr-line>Departments of Neurology and Physiology/Pharmacology, State University New York Downstate Medical Center, Brooklyn, New York, United States of America</addr-line></nlm:aff></affiliation></author><author><name sortKey="Petersen, Robert" sort="Petersen, Robert" uniqKey="Petersen R" first="Robert" last="Petersen">Robert Petersen</name><affiliation><nlm:aff id="aff2"><addr-line>Departments of Pathology, Neuroscience, and Neurology, Case Western Reserve University, Cleveland, Ohio, United States of America</addr-line></nlm:aff></affiliation></author><author><name sortKey="Wisniewski, Thomas" sort="Wisniewski, Thomas" uniqKey="Wisniewski T" first="Thomas" last="Wisniewski">Thomas Wisniewski</name><affiliation><nlm:aff id="aff3"><addr-line>Departments of Neurology, Psychiatry and Pathology, New York University School of Medicine, New York, New York, United States of America</addr-line></nlm:aff></affiliation></author><author><name sortKey="Rubenstein, Richard" sort="Rubenstein, Richard" uniqKey="Rubenstein R" first="Richard" last="Rubenstein">Richard Rubenstein</name><affiliation><nlm:aff id="aff1"><addr-line>Departments of Neurology and Physiology/Pharmacology, State University New York Downstate Medical Center, Brooklyn, New York, United States of America</addr-line></nlm:aff></affiliation></author></analytic><series><title level="j">PLoS ONE</title><idno type="eISSN">1932-6203</idno><imprint><date when="2012">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>PrP<sup>Sc</sup> is believed to serve as a template for the conversion of PrP<sup>C</sup> to the abnormal isoform. This process requires contact between the two proteins and implies that there may be critical contact sites that are important for conversion. We hypothesized that antibodies binding to either PrP<sup>c</sup>or PrP<sup>Sc</sup> would hinder or prevent the formation of the PrP<sup>C</sup>–PrP<sup>Sc</sup> complex and thus slow down or prevent the conversion process. Two systems were used to analyze the effect of different antibodies on PrP<sup>Sc</sup> formation: (i) neuroblastoma cells persistently infected with the 22L mouse-adapted scrapie stain, and (ii) protein misfolding cyclic amplification (PMCA), which uses PrP<sup>Sc</sup> as a template or seed, and a series of incubations and sonications, to convert PrP<sup>C</sup> to PrP<sup>Sc</sup>. The two systems yielded similar results, in most cases, and demonstrate that PrP-specific monoclonal antibodies (Mabs) vary in their ability to inhibit the PrP<sup>C</sup>–PrP<sup>Sc</sup> conversion process. Based on the numerous and varied Mabs analyzed, the inhibitory effect does not appear to be epitope specific, related to PrP<sup>C</sup> conformation, or to cell membrane localization, but is influenced by the targeted PrP region (amino vs carboxy).</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Caughey, Bw" uniqKey="Caughey B">BW Caughey</name></author><author><name sortKey="Dong, A" uniqKey="Dong A">A Dong</name></author><author><name sortKey="Bhat, Ks" uniqKey="Bhat K">KS Bhat</name></author><author><name sortKey="Ernst, D" uniqKey="Ernst D">D Ernst</name></author><author><name sortKey="Hayes, Sf" uniqKey="Hayes S">SF Hayes</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Gasset, M" uniqKey="Gasset M">M Gasset</name></author><author><name sortKey="Baldwin, Ma" uniqKey="Baldwin M">MA Baldwin</name></author><author><name sortKey="Fletterick, Rj" uniqKey="Fletterick R">RJ 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<front><journal-meta><journal-id journal-id-type="nlm-ta">PLoS One</journal-id><journal-id journal-id-type="iso-abbrev">PLoS ONE</journal-id><journal-id journal-id-type="publisher-id">plos</journal-id><journal-id journal-id-type="pmc">plosone</journal-id><journal-title-group><journal-title>PLoS ONE</journal-title></journal-title-group><issn pub-type="epub">1932-6203</issn><publisher><publisher-name>Public Library of Science</publisher-name><publisher-loc>San Francisco, USA</publisher-loc></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">22848548</article-id><article-id pub-id-type="pmc">3407222</article-id><article-id pub-id-type="publisher-id">PONE-D-12-13547</article-id><article-id pub-id-type="doi">10.1371/journal.pone.0041626</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Biology</subject><subj-group><subject>Biochemistry</subject><subj-group><subject>Proteins</subject><subj-group><subject>Transmembrane Proteins</subject></subj-group></subj-group></subj-group><subj-group><subject>Immunology</subject><subj-group><subject>Immunity</subject><subj-group><subject>Immunotherapy</subject></subj-group></subj-group><subj-group><subject>Immunologic Subspecialties</subject><subj-group><subject>Neuroimmunology</subject></subj-group></subj-group><subj-group><subject>Immunoglobulins</subject><subject>Immunomodulation</subject></subj-group></subj-group><subj-group><subject>Neuroscience</subject></subj-group></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine</subject><subj-group><subject>Infectious Diseases</subject><subj-group><subject>Prion Diseases</subject></subj-group></subj-group><subj-group><subject>Neurology</subject><subj-group><subject>Infectious Diseases of the Nervous System</subject><subject>Neurodegenerative Diseases</subject></subj-group></subj-group></subj-group></article-categories><title-group><article-title>Influence of Mabs on PrP<sup>Sc</sup> Formation Using <italic>In Vitro</italic> and Cell-Free Systems</article-title><alt-title alt-title-type="running-head">Mab Effects on PrP<sup>Sc</sup> in Cells and Cell-Free Models</alt-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Chang</surname><given-names>Binggong</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author"><name><surname>Petersen</surname><given-names>Robert</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author"><name><surname>Wisniewski</surname><given-names>Thomas</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib><contrib contrib-type="author"><name><surname>Rubenstein</surname><given-names>Richard</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib></contrib-group><aff id="aff1"><label>1</label><addr-line>Departments of Neurology and Physiology/Pharmacology, State University New York Downstate Medical Center, Brooklyn, New York, United States of America</addr-line></aff><aff id="aff2"><label>2</label><addr-line>Departments of Pathology, Neuroscience, and Neurology, Case Western Reserve University, Cleveland, Ohio, United States of America</addr-line></aff><aff id="aff3"><label>3</label><addr-line>Departments of Neurology, Psychiatry and Pathology, New York University School of Medicine, New York, New York, United States of America</addr-line></aff><contrib-group><contrib contrib-type="editor"><name><surname>Rezaei</surname><given-names>Human</given-names></name><role>Editor</role><xref ref-type="aff" rid="edit1"></xref></contrib></contrib-group><aff id="edit1"><addr-line>National Institute for Agricultural Research, France</addr-line></aff><author-notes><corresp id="cor1">* E-mail: <email>richard.rubenstein@downstate.edu</email></corresp><fn fn-type="COI-statement"><p><bold>Competing Interests: </bold>TW is a PLoS ONE Editorial Board member. This does not alter the authors’ adherence to all the PLoS ONE policies on sharing data and materials.</p></fn><fn fn-type="con"><p>Conceived and designed the experiments: RR TW. Performed the experiments: BC RP TW RR. Analyzed the data: BC RP TW RR. Contributed reagents/materials/analysis tools: RP TW RR. Wrote the paper: RR.</p></fn></author-notes><pub-date pub-type="collection"><year>2012</year></pub-date><pub-date pub-type="epub"><day>27</day><month>7</month><year>2012</year></pub-date><volume>7</volume><issue>7</issue><elocation-id>e41626</elocation-id><history><date date-type="received"><day>1</day><month>5</month><year>2012</year></date><date date-type="accepted"><day>22</day><month>6</month><year>2012</year></date></history><permissions><copyright-statement>© 2012 Chang et al</copyright-statement><copyright-year>2012</copyright-year><copyright-holder>Chang et al</copyright-holder><license xlink:href="http://creativecommons.org/licenses/by/4.0/"><license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.</license-p></license></permissions><abstract><p>PrP<sup>Sc</sup> is believed to serve as a template for the conversion of PrP<sup>C</sup> to the abnormal isoform. This process requires contact between the two proteins and implies that there may be critical contact sites that are important for conversion. We hypothesized that antibodies binding to either PrP<sup>c</sup>or PrP<sup>Sc</sup> would hinder or prevent the formation of the PrP<sup>C</sup>–PrP<sup>Sc</sup> complex and thus slow down or prevent the conversion process. Two systems were used to analyze the effect of different antibodies on PrP<sup>Sc</sup> formation: (i) neuroblastoma cells persistently infected with the 22L mouse-adapted scrapie stain, and (ii) protein misfolding cyclic amplification (PMCA), which uses PrP<sup>Sc</sup> as a template or seed, and a series of incubations and sonications, to convert PrP<sup>C</sup> to PrP<sup>Sc</sup>. The two systems yielded similar results, in most cases, and demonstrate that PrP-specific monoclonal antibodies (Mabs) vary in their ability to inhibit the PrP<sup>C</sup>–PrP<sup>Sc</sup> conversion process. Based on the numerous and varied Mabs analyzed, the inhibitory effect does not appear to be epitope specific, related to PrP<sup>C</sup> conformation, or to cell membrane localization, but is influenced by the targeted PrP region (amino vs carboxy).</p></abstract><funding-group><funding-statement>This work was supported in part by the State University New York Downstate Medical Center, National Institutes of Health grant NS47433 (TW) and grant NP020048 from the United States Department of Defense National Prion Research Program. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.</funding-statement></funding-group><counts><page-count count="7"></page-count></counts></article-meta></front><body><sec id="s1"><title>Introduction</title><p>Prion diseases are a group of fatal neurodegenerative disorders that are associated with conformational conversion of the cellular prion protein, PrP<sup>C</sup>, which is mainly α-helical with very few beta sheets, into a β-sheet-rich form, PrP<sup>Sc</sup><xref rid="pone.0041626-Caughey1" ref-type="bibr">[1]</xref>–<xref rid="pone.0041626-Colby1" ref-type="bibr">[5]</xref>. The mechanism by which PrP<sup>C</sup> is converted to the abnormal isoform is still not clear, but it is presumed to involve a PrP<sup>C</sup>–PrP<sup>Sc</sup> complex, with the latter serving as a conformational template <xref rid="pone.0041626-Prusiner1" ref-type="bibr">[6]</xref>. In this model, PrP<sup>Sc</sup> serves as a template that binds to PrP<sup>C</sup> and produces a conformational conversion into the abnormal isoform. This raises the issue of whether there are critical contact sites that mediate conversion. If this is the case, interfering with or blocking complex formation should prevent the PrP<sup>C</sup> to PrP<sup>Sc</sup> conversion process. Previous reports have described anti-PrP antibodies that can stop or hinder the conversion process add reference 44 and renumber <xref rid="pone.0041626-Enari1" ref-type="bibr">[7]</xref>–<xref rid="pone.0041626-Horiuchi1" ref-type="bibr">[14]</xref>.</p><p>Protein misfolding cyclic amplification (PMCA) is an assay that mimics the PrP<sup>Sc</sup> propagation process under cell-free conditions. In this method PrP<sup>Sc</sup> is amplified by converting PrP<sup>C</sup> to a PrP<sup>Sc</sup> seed during incubation with periodic sonication <xref rid="pone.0041626-Saborio1" ref-type="bibr">[15]</xref>. PrP<sup>Sc</sup> generated by PMCA is infectious in wild-type animals <xref rid="pone.0041626-Castilla1" ref-type="bibr">[16]</xref> and can be indefinitely propagated while preserving the properties of the original PrP<sup>Sc</sup> strain <xref rid="pone.0041626-Castilla1" ref-type="bibr">[16]</xref>–<xref rid="pone.0041626-Shikiya1" ref-type="bibr">[18]</xref>. Furthermore, PMCA has been quite useful in studying the cofactors that influence PrP conversion <xref rid="pone.0041626-Kim1" ref-type="bibr">[19]</xref>–<xref rid="pone.0041626-Mays2" ref-type="bibr">[26]</xref>, and in detecting PrP<sup>Sc</sup> from biological samples of humans and animals <xref rid="pone.0041626-Castilla2" ref-type="bibr">[17]</xref>, <xref rid="pone.0041626-Soto1" ref-type="bibr">[27]</xref>–<xref rid="pone.0041626-Murayama2" ref-type="bibr">[34]</xref>.</p><p>We hypothesized that antibodies binding to PrP<sup>c</sup> and/or PrP<sup>Sc</sup> might hinder or prevent the formation of the PrP<sup>C</sup>–PrP<sup>Sc</sup> complex and thus prevent the conversion process. We compared the effect of individual PrP-specific monoclonal antibodies (Mabs) on the PrP<sup>C</sup>–PrP<sup>Sc</sup> conversion process using both an N2a/22L cell culture model and the test-tube PMCA system. Our results demonstrate that the Mabs have a range of inhibitory effects on the PrP<sup>C</sup>–PrP<sup>Sc</sup> conversion process. The degree of inhibition is Mab specific and more dependent on the antibody targeting region than on the specific epitope being recognized. Furthermore, since the PMCA-based method is dose-dependent and rapid, it may serve as an ideal screening assay for potential inhibitors of both PrP<sup>Sc</sup> accumulation and the progression of prion diseases.</p></sec><sec sec-type="methods" id="s2"><title>Methods</title><sec id="s2a"><title>Animals (Ethics Statement)</title><p>All procedures involving animals and their care were conducted in accordance with the United States Department of Agriculture Animal Welfare Act and the National Institute of Health policy on Humane Care and Use of Laboratory Animals. Tissue samples from uninfected and prion agent-infected mice and hamsters were obtained using protocols approved by the Institutional Animal Care and Use Committee of the SUNY Downstate Medical Center (protocol #’s 07-250-09 and 07-251-09).</p></sec><sec id="s2b"><title>PMCA and Western Blotting</title><p>A 10% normal hamster brain homogenate (NBH) was prepared in phosphate buffered saline (PBS) containing 1% Triton X-100, 4mM EDTA and 1% protease inhibitor cocktail (Abcam). PrP-specific Mabs were generated against recombinant (murine or hamster) PrP or brain-derived proteinase K (PK)-resistant purified PrP<sup>Sc</sup><xref rid="pone.0041626-Hilmert1" ref-type="bibr">[35]</xref> from brains of clinical mice infected with the ME7 mouse-adapted scrapie strain or clinical hamsters infected with the 263K hamster-adapted scrapie strain. The Mabs used in this study were purified (Montage Antibody Purification kit; Millipore, Billerica, CA), isotyped (ELISA Mouse Antibody Isotyping kit; Thermo Fisher, Rockford, IL), and epitope mapped (<xref ref-type="table" rid="pone-0041626-t001">Table 1</xref>). The immunoreactivity of all the Mabs were analyzed on western blots against denatured, PK-digested and undigested PrP derived from uninfected and infected brain homogenates as well as by ELISA against recombinant PrP. With the exception of Mab 3F4, each of the individual Mabs had equivalent immunoreactivity against murine and hamster PrP<sup>Sc</sup> on an immunoglobulin concentration basis. All of the Mabs were highly reactive against both hamster PrP<sup>C</sup> and PrP<sup>Sc</sup> isoforms and, for the PMCA studies, were individually added to the 10% NBH at a final concentrations of 50 µg/ml. A 10% 263K brain homogenate was prepared in PBS only and diluted to a final concentration of 10<sup>−4</sup>. A 100 µl aliquot of this homogenate was initially combined with 10 µl of 10% NBH (with or without added Mab). Each sample was sonicated (QSONIC at 480W power, 60 Amplitude, 40,000 J energy, 90 sec process time, 3 sec pulse on−1 sec pulse off), then incubated at 37°C for 1 hr. This was defined as one cycle of serial PMCA (sPMCA). At the completion of each cycle, an additional 10 µl of 10% NBH (with or without Mab) was added. At the end of every five cycles, 100 µl of the total volume was transferred to a new tube containing an equal volume of 10% NBH (with or without Mab) and the cycling reactions continued. At the completion of 40 cycles (sPMCA<sub>40</sub>), 500 µl from each sample was PK-treated (100 µg/ml final concentration, 50°C, 30 min), followed by the addition of protease inhibitor cocktail. The sample was heated (100°C, 10 min) and then centrifuged at 16,000×g for 2 min at room temperature. The supernatant was combined with 6X Laemmli sample buffer, and 50 µl was electrophoresed in a 12% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) followed by transfer to nitrocellulose membrane. The membrane was blocked for 1 hr in PBS containing 0.1% Tween 20 (PBST) with 5% non-fat dry milk and incubated with 2 µg/ml biotinylated Mab 08-6/2F11. The membrane was washed 3 times (10 min each) with PBST, incubated for 60 min in HRP-conjugated streptavidin (Invitrogen) (1∶5000 in PBST containing 5% non-fat dry milk) followed by 3 additional PBST washes and detection of proteins with ECL Supersignal West Dura kit (Thermo Fisher). Quantification of PrP<sup>Sc</sup> was performed by densitometric analysis using NIH Image J software.</p><table-wrap id="pone-0041626-t001" orientation="portrait" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0041626.t001</object-id><label>Table 1</label><caption><title>Characterization of Mabs.</title></caption><alternatives><graphic id="pone-0041626-t001-1" xlink:href="pone.0041626.t001"></graphic><table frame="hsides" rules="groups"><colgroup span="1"><col align="left" span="1"></col><col align="center" span="1"></col><col align="center" span="1"></col><col align="center" span="1"></col><col align="center" span="1"></col><col align="center" span="1"></col></colgroup><thead><tr><td colspan="2" align="left" rowspan="1">Mab</td><td align="left" rowspan="1" colspan="1">Isotype</td><td align="left" rowspan="1" colspan="1">Epitope</td><td colspan="2" align="left" rowspan="1">Immunoreactivity</td></tr><tr><td align="left" rowspan="1" colspan="1"></td><td align="left" rowspan="1" colspan="1"></td><td align="left" rowspan="1" colspan="1"></td><td align="left" rowspan="1" colspan="1"></td><td align="left" rowspan="1" colspan="1">Mse PrP<sup>C</sup>/PrP<sup>Sc</sup></td><td align="left" rowspan="1" colspan="1">Ham. PrP<sup>C</sup>/PrP<sup>Sc</sup></td></tr></thead><tbody><tr><td align="left" rowspan="1" colspan="1">08-6/7E4</td><td align="left" rowspan="1" colspan="1">(7E4)</td><td align="left" rowspan="1" colspan="1">IgG1</td><td align="left" rowspan="1" colspan="1">aa 29–35</td><td align="left" rowspan="1" colspan="1">+/+</td><td align="left" rowspan="1" colspan="1">+/+</td></tr><tr><td align="left" rowspan="1" colspan="1">01-7/10E4</td><td align="left" rowspan="1" colspan="1">(10E4)</td><td align="left" rowspan="1" colspan="1">IgG1</td><td align="left" rowspan="1" colspan="1">aa 54–89</td><td align="left" rowspan="1" colspan="1">+/+</td><td align="left" rowspan="1" colspan="1">+/+</td></tr><tr><td align="left" rowspan="1" colspan="1">08-1/5D6</td><td align="left" rowspan="1" colspan="1">(5D6)</td><td align="left" rowspan="1" colspan="1">IgG2b</td><td align="left" rowspan="1" colspan="1">aa 91–101</td><td align="left" rowspan="1" colspan="1">+/+</td><td align="left" rowspan="1" colspan="1">+/+</td></tr><tr><td align="left" rowspan="1" colspan="1">08-1/11F12</td><td align="left" rowspan="1" colspan="1">(11F12)</td><td align="left" rowspan="1" colspan="1">IgG2b</td><td align="left" rowspan="1" colspan="1">aa 91–111</td><td align="left" rowspan="1" colspan="1">+/+</td><td align="left" rowspan="1" colspan="1">+/+</td></tr><tr><td align="left" rowspan="1" colspan="1">3F4</td><td align="left" rowspan="1" colspan="1"></td><td align="left" rowspan="1" colspan="1">IgG2a</td><td align="left" rowspan="1" colspan="1">aa 107–112</td><td align="left" rowspan="1" colspan="1">−/−</td><td align="left" rowspan="1" colspan="1">+/+</td></tr><tr><td align="left" rowspan="1" colspan="1">03-9/8E11</td><td align="left" rowspan="1" colspan="1">(8E11)</td><td align="left" rowspan="1" colspan="1">IgG2a</td><td align="left" rowspan="1" colspan="1">aa 112–120</td><td align="left" rowspan="1" colspan="1">+/+</td><td align="left" rowspan="1" colspan="1">+/+</td></tr><tr><td align="left" rowspan="1" colspan="1">02-3/3A2</td><td align="left" rowspan="1" colspan="1">(3A2)</td><td align="left" rowspan="1" colspan="1">IgG1</td><td align="left" rowspan="1" colspan="1">aa 121–125</td><td align="left" rowspan="1" colspan="1">+/+</td><td align="left" rowspan="1" colspan="1">+/+</td></tr><tr><td align="left" rowspan="1" colspan="1">08-1/8E9</td><td align="left" rowspan="1" colspan="1">(8E9)</td><td align="left" rowspan="1" colspan="1">IgG2b</td><td align="left" rowspan="1" colspan="1">aa 135–153</td><td align="left" rowspan="1" colspan="1">+/+</td><td align="left" rowspan="1" colspan="1">+/+</td></tr><tr><td align="left" rowspan="1" colspan="1">01-16/1B11</td><td align="left" rowspan="1" colspan="1">(1B11)</td><td align="left" rowspan="1" colspan="1">IgG2a</td><td align="left" rowspan="1" colspan="1">aa 141–145</td><td align="left" rowspan="1" colspan="1">+/+</td><td align="left" rowspan="1" colspan="1">+/+</td></tr><tr><td align="left" rowspan="1" colspan="1">01-7/2F7</td><td align="left" rowspan="1" colspan="1">(2F7)</td><td align="left" rowspan="1" colspan="1">IgG1</td><td align="left" rowspan="1" colspan="1">aa 193–210</td><td align="left" rowspan="1" colspan="1">+/+</td><td align="left" rowspan="1" colspan="1">+/+</td></tr></tbody></table></alternatives></table-wrap></sec><sec id="s2c"><title>Epitope Mapping</title><p>Cellulose membranes spotted with 99 overlapping 13-mer PrP peptides were produced as previously described <xref rid="pone.0041626-Guo1" ref-type="bibr">[36]</xref>. The membranes were blocked with 5% non-fat dry milk/tris-buffered saline containing 0.1% Tween 20 (TBST) probed with antibody diluted 1∶5000 in 1% normal goat serum/TBS at 4°C overnight, followed by horseradish peroxidase (HRP)-conjugated goat anti-mouse secondary (Cappel 55570) for 2 hours at room temperature, and detected using Millipore Immobilon Western chemiluminescent HRP substrate (Cat WBKLS0500). Membranes were regenerated for re-use by shaking with dimethylformamide for 30 minutes, then 8M urea/50mM Tris-HCl pH 8.0/1% β-mercaptoethanol (β-MC)/1%SDS overnight at 37°C, followed by a 30 min wash in the same buffer, and then twice for 30 minutes each in 50% methanol/glacial acetic acid, and finally three times for 5 minutes each in methanol. After air drying membranes were stored in a sealed container at room temperature.</p></sec><sec id="s2d"><title>Infection and Mab Treatment of N2a Cells</title><p>Murine neuroblastoma N2a cells (ATCC line CCL 131) were grown in the Minimal Essential Medium supplemented with 10% FBS, penicillin and streptomycin and infected with 2% 22L brain homogenate as described previously <xref rid="pone.0041626-Pankiewicz1" ref-type="bibr">[12]</xref>. Following infection, the amount of PrP<sup>Sc</sup> in 200 µg cell lysate aliquots of the N2a/22L cells was determined by PK digestion (1 µg/µl PK for 30 min at 37°C), SDS-PAGE on 12.5% Tris-tricine gels <xref rid="pone.0041626-JimnezHuete1" ref-type="bibr">[37]</xref> and western blot analysis as previously described <xref rid="pone.0041626-Pankiewicz1" ref-type="bibr">[12]</xref>.</p><p>For treatment of cells with Mabs, N2a/22L cells (from the fifth passage after infection and higher) were plated in six-well plates and once the cells were 70–80% confluent, Mabs were added at a final concentration of 10 µg/ml and incubation was continued for 96 hr. Each Mab was tested in three independent experiments using independently infected cell lines. Each experiment included both a positive control (untreated N2a/22L cells) and a negative control (N2a cells), which were subjected to PK digestion. The level of PK-resistant PrP<sup>Sc</sup> was measured in western blots using HRP-conjugated sheep anti-mouse IgG as the secondary reagent and ECL Supersignal West Dura kit. Membranes were exposed to X-ray film (X-Omat Blue XB-1; Kodak, New Haven, CT,) with a constant exposure time of 30 sec. The films were converted into eight-bit grayscale digital files. Quantification of PrP<sup>Sc</sup> was performed by densitometric analysis using NIH Image J software v. 1.34. Areas under the curves for three PrP bands representing non-, mono-and diglycosylated isoforms of the protein were summarized from each sample to calculate the total amount of PrP and expressed as percentages of the average value from a positive control (untreated N2a/22L), whereas the optic density of the background was taken from negative control lanes (N2a cells).</p></sec></sec><sec id="s3"><title>Results</title><p>The PrP-specific Mabs that were evaluated for their ability to prevent PrP<sup>C</sup> to PrP<sup>Sc</sup> conversion have linear epitopes that span the entire prion protein from the amino to the carboxy terminus (<xref ref-type="table" rid="pone-0041626-t001">Table 1</xref>, <xref ref-type="fig" rid="pone-0041626-g001">Fig. 1</xref>).</p><fig id="pone-0041626-g001" orientation="portrait" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0041626.g001</object-id><label>Figure 1</label><caption><title>Linear diagram of prion protein showing epitope location of PrP-specific monoclonal antibodies used on N2a/22L cells and in PMCA.</title></caption><graphic xlink:href="pone.0041626.g001"></graphic></fig><p>We used N2a cells persistently infected with the 22L mouse-adapted scrapie strain (N2a/22L) to evaluate the affect of each Mab on PrP<sup>Sc</sup> formation (<xref ref-type="fig" rid="pone-0041626-g002">Fig. 2A and 2B</xref>). Treatment with the Mabs did not result in any cytotoxicity to the N2a/22L cells throughout the incubation period. Further, incubation of the. N2a/22L cells with 10 µg/ml purified, irrelevant mouse IgG had no effect on PrP<sup>Sc</sup> formation compared to untreated N2a/22L cultures (<xref ref-type="fig" rid="pone-0041626-g002">Figs. 2A and 2B</xref>). Mab 3F4 did not reduce PrP<sup>Sc</sup> formation compared to control N2a/22L cultures lacking Mab. Mab 3F4 does not react with mouse prion protein so this was not surprising <xref rid="pone.0041626-Rubenstein2" ref-type="bibr">[38]</xref>. The ability of a singly added Mab to inhibit PrP<sup>Sc</sup> formation was not related to a specific epitope since all of the remaining singly added Mabs inhibited PrP<sup>Sc</sup> formation to varying degrees. Of the individually added Mabs, 5D6 was the most effective at inhibiting PrP<sup>Sc</sup> formation (95% inhibition) while 3A2 was the least effective (38% inhibition). Targeting the amino terminus with Mab 7E4 was effective at inhibiting 73% PrP<sup>Sc</sup> formation as was targeting the octapeptide repeat region using Mab 10E4 which resulted in almost 90% inhibition. Strangely, although their epitopes overlap, Mab 11F12 was less effective than Mab 5D6 at inhibiting PrP<sup>Sc</sup> formation (53% vs 95% inhibition). This is in contrast to Mabs 8E9 and 1B11, which have overlapping epitopes with 8E9 being more expansive, and resulted in 52% and 42% inhibition, respectively. The combination of 5D6 and 11F12 did not result in an additive inhibitory effect and, in fact, resulted in less inhibition than either one alone. This was confirmed in studies where the addition of 8E9 to 5D6 and 11F12 caused a 45% PrP<sup>Sc</sup> inhibition, which was slightly better than 8E9 alone, although the predicted additive inhibitory effect of 63% for the three Mab combination (48% for 8E9 plus 15% for the 5D6 and 11F12 combination) was not observed.</p><fig id="pone-0041626-g002" orientation="portrait" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0041626.g002</object-id><label>Figure 2</label><caption><title>A. Mab Inhibition of PrP<sup>Sc</sup> in N2a/22L Cells.</title><p>N2a/22L cells were incubated with purified Mabs for 96 hrs. Cells were harvested and PK-treated lysates were western blotted (<bold>see</bold><xref ref-type="fig" rid="pone-0041626-g002"><bold>Figure 2B</bold></xref><bold>for representative western blots</bold>). PrP<sup>Sc</sup> western blots were quantitated and the amount of inhibition was determined relative to N2a/22L control cultures. The controls consisted of cells both in the absence of Mab and in the presence of normal mouse IgG. The % PrP<sup>Sc</sup> inhibition plotted represents the mean ± SD from three independent experiments as described in Methods.</p></caption><graphic xlink:href="pone.0041626.g002"></graphic></fig><p>Studies were performed with PMCA to determine whether a cell-free system can recapitulate the effect of Mabs on PrP<sup>C</sup> conversion observed in infected cells. This system also allowed us to evaluate whether accessibility of Mab to membrane associated PrP<sup>C</sup> in the living cells influences the PrP<sup>C</sup> to PrP<sup>Sc</sup> conversion process. Mabs (12–50 µg/ml final concentration) were added throughout the sPMCA<sub>40</sub> protocol along with the 10% NBH spiked with a 10<sup>−4</sup> dilution of 263K infected brain homogenate as described in the Methods section. This dilution of infected brain homogenate does not result in detectable PK resistant PrP<sup>Sc</sup> immunostaining (<xref ref-type="fig" rid="pone-0041626-g003">Fig. 3A</xref>) and, therefore, did not interfere with the detection of newly formed PrP<sup>Sc</sup>. At the completion of sPMCA<sub>40</sub>, the samples were digested with PK (100 µg/ml) and analyzed on immunoblots using biotinylated Mab 2F11 which reacts equally with both hamster PrP<sup>C</sup> and PrP<sup>Sc</sup>. It is interesting to note that although the 263K-infected brain homogenate displayed the 3 band pattern typical for the multiple glycosylated forms of PrP<sup>C</sup> and PrP<sup>Sc</sup> (<xref ref-type="fig" rid="pone-0041626-g003">Fig. 3A</xref>), the sPMCA<sub>40</sub> products in the positive controls and Mab-treated reactions consisted of only a single diglycosylated 30 kDa PrP<sup>Sc</sup> band observed after PK digestion at the higher levels of inhibition, >50%, but had two bands or a smear when there was less inhibition (<xref ref-type="fig" rid="pone-0041626-g003">Fig. 3B</xref>).</p><fig id="pone-0041626-g003" orientation="portrait" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0041626.g003</object-id><label>Figure 3</label><caption><title>A. Western blot of 263K brain homogenate that was used as the seed for PMCA.</title><p>Dilutions of the brain homogenate was prepared and either untreated (lanes 1 and 2) or PK-treated (lanes 3 and 4) prior to SDS-PAGE and western blotting. A 10−3 dilution prior to and after PK demonstrates the three protein banding pattern typical for 263K brain homogenate whereas no bands are visible at a 10−4 dilution of the same homogenate. <bold>B.</bold> Western blotting of the PMCA products following sPMCA40 in the absence and presence of PrP-Specific Mabs. Fourty cycles of serial PMCA was carried out in the absence or presence of Mabs as described in the text. Each Mab was added at a final concentration of 12, 25, and 50 µg/ml. Following PK treatment, the PMCA products were subjected to SDS-PAGE, western blotted and immunostained for PrPSc. The protein bands were quantitated and the level of PrPSc inhibition, relative to the no Mab and normal mouse IgG controls, were determined.</p></caption><graphic xlink:href="pone.0041626.g003"></graphic></fig><p>PMCA in the presence of Mabs was also used to study the importance of binding site specificity in the PrP<sup>C</sup> to PrP<sup>Sc</sup> conversion process (<xref ref-type="fig" rid="pone-0041626-g003">Fig. 3</xref>). We performed sPMCA with different Mab concentrations to determine the minimum amount of Mab necessary to inhibit the conversion process. Using a 10<sup>−4</sup> dilution of 263K-infected hamster brain homogenate as the PrP<sup>Sc</sup> seed and a 10% normal brain homogenate (NBH) as the source of PrP<sup>C</sup>, we tested the ability of Mabs to inhibit the conversion of PrP<sup>C</sup> to PrP<sup>Sc</sup>. For each Mab, final concentrations of 12 µg/ml (lanes 3, 6, 9, 12, 15, 18, 21 and 24), 25 µg/ml (lanes 4, 7, 10, 13, 16, 19, 22 and 25) and 50 µg/ml (lanes 5, 8, 11, 14, 17, 20, 23, and 26) were prepared in hamster NBH and used in the sPMCA reactions. Compared to sPMCA<sub>40</sub>, which contained no Mab (lane 1) and with the exception of 02–3/3A2, the majority of the PrP-specific Mabs inhibited the conversion process in a dose-related manner although some were more effective than others. Mabs 7E4, 10E4, 11F12, 8E11, and 8E9 completely inhibited the conversion process at 50 µg/ml while Mabs 1B11 and 2F7 inhibited the conversion process to a lesser degree. The inhibition caused by the Mabs was a specific response since sPMCA<sub>40</sub> studies replacing Mabs with purified normal mouse IgG (at 12–50 µg/ml) in the 10% NBH did not cause any inhibition of PrP<sup>Sc</sup> formation (data not shown). It is interesting to note that, with the exception of only 8E9, the epitopes for all the Mabs that caused complete inhibition are located in the amino half of the PrP while those that caused incomplete inhibition are located in the carboxy half of PrP. There was good correlation between the extent of PrP<sup>Sc</sup> inhibition when 10 µg/ml Mab in cell culture was compared to 12 µg/ml Mab with sPMCA<sub>40</sub>.</p><p>A separate study using sPMCA<sub>40</sub> demonstrated that Mabs 3F4 and 5D6 caused complete inhibition of PrP<sup>Sc</sup> formation at 12–50 µg/ml (<xref ref-type="fig" rid="pone-0041626-g004">Fig. 4</xref>). Therefore we extended those studies and evaluated the effects of Mabs 3F4 and 5D6 using a wider range of Mab concentrations (1.5–50 µg/ml). Compared to the other antibodies in this study, Mabs 3F4 and 5D6 had the most pronounced effects on PrP<sup>Sc</sup> formation as demonstrated by the low concentrations of 3 and 6 µg/ml, respectively, causing complete inhibition (<xref ref-type="fig" rid="pone-0041626-g004">Fig. 4</xref>). The potent inhibitory effect of 5D6 on PrP<sup>Sc</sup> observed using sPMCA<sub>40</sub> coincides with its dramatic effect in the N2a/22L culture model. Furthermore, the poor PrP<sup>Sc</sup> inhibition by 3A2 with sPMCA<sub>40</sub> (<xref ref-type="fig" rid="pone-0041626-g003">Fig. 3B</xref>) corresponded well with the poor inhibition (only 32% reduction compared to negative control) observed in the cell culture system (<xref ref-type="fig" rid="pone-0041626-g002">Fig. 2A and 2B</xref>).</p><fig id="pone-0041626-g004" orientation="portrait" position="float"><object-id pub-id-type="doi">10.1371/journal.pone.0041626.g004</object-id><label>Figure 4</label><caption><title>Influence of Mabs 3F4 and 5D6 on PrP<sup>Sc</sup> formation following sPMCA<sub>40</sub>.</title><p>Mabs 3F4 and 5D6 were added to sPMCA<sub>40</sub> at final concentrations of 0–50 µg/ml. The PMCA products were PK treated and western blotted. The PrP<sup>Sc</sup> was quantitated and the level of PrP<sup>Sc</sup> inhibition was determined relative to control reactions.</p></caption><graphic xlink:href="pone.0041626.g004"></graphic></fig></sec><sec id="s4"><title>Discussion</title><p>Currently, there is no effective treatment for prion diseases. To date, hundreds of chemical compounds have been identified that antagonize prion propagation <italic>in vitro</italic> in cell culture-based assays and/or <italic>in vivo</italic> in animal studies <xref rid="pone.0041626-Brown1" ref-type="bibr">[39]</xref>–<xref rid="pone.0041626-Sim1" ref-type="bibr">[43]</xref>. Unfortunately, many compounds efficient in <italic>in vitro</italic> studies were only effective in animal models if treatment was begun before or close to the time of inoculation with the infectious agent <xref rid="pone.0041626-Priola1" ref-type="bibr">[44]</xref>. Furthermore, many of the candidate compounds have limited usefulness clinically due to toxicity or their inability to cross the blood-brain barrier [e.g. Congo red <xref rid="pone.0041626-Rudyk1" ref-type="bibr">[45]</xref>, iododoxorubicin, β-sheet breakers].</p><p>Additional therapeutic and/or prophylactic strategies have been and continue to be pursued. Vaccination with recombinant mouse PrP delays the onset of prion disease in mice <xref rid="pone.0041626-Sigurdsson2" ref-type="bibr">[46]</xref>. Passive immunization with anti-PrP antibodies was shown not only to inhibit formation of PrP<sup>Sc</sup> in a cell-free system <xref rid="pone.0041626-Kim3" ref-type="bibr">[47]</xref>, but was also shown to prevent infection of susceptible N2a cells <xref rid="pone.0041626-Enari1" ref-type="bibr">[7]</xref> and to inhibit prion replication in infected cells <xref rid="pone.0041626-Peretz1" ref-type="bibr">[8]</xref>, <xref rid="pone.0041626-Kim3" ref-type="bibr">[47]</xref>, <xref rid="pone.0041626-Perrier1" ref-type="bibr">[48]</xref>. The effectiveness of these treatments were also dependent on when they were administered relative to the time of infection.</p><p>In an initial passive immunization study using wild-type CD1 mice, Mabs 8B4 (to mouse PrP residues 34–52) and 8H4 (to mouse PrP residues 175–185) given immediately after challenge with 139A scrapie by intraperitoneal (IP) injection (50 µg/week), resulted in a significant prolongation of the incubation period with 10% of the 8B4 treated animals remaining disease free in the group challenged with a lower dose of PrP<sup>Sc</sup><xref rid="pone.0041626-Sigurdsson1" ref-type="bibr">[10]</xref>. In another study using higher antibody doses (4000 µg/week IP) of either ICSM 18 (to mouse PrP residues 146–158) or ICSM 35 (to mouse residues 95 to 105), prion infection from a peripheral source was completely prevented if treatment was continued for 7 or 30 days immediately following PrP<sup>Sc</sup> challenge <xref rid="pone.0041626-White1" ref-type="bibr">[9]</xref>. Furthermore, a transgenic mouse model that expresses Mab 6H4 is resistant to prion infection via IP injection by a mechanism that involves either perturbation of cellular PrP trafficking/PrP<sup>C</sup> degradation or disruption of the PrP<sup>C</sup>–PrP<sup>Sc</sup> interaction <xref rid="pone.0041626-Heppner1" ref-type="bibr">[49]</xref>.</p><p>Previous studies have reported that the 132–140 portion of PrP<sup>C</sup><xref rid="pone.0041626-Peretz1" ref-type="bibr">[8]</xref> or the 132–156 region of PrP <xref rid="pone.0041626-Scott1" ref-type="bibr">[50]</xref>–<xref rid="pone.0041626-Priola3" ref-type="bibr">[53]</xref> are important for the generation of PrP<sup>Sc</sup>. Rigter et al. <xref rid="pone.0041626-Rigter1" ref-type="bibr">[54]</xref> found two high affinity binding regions for protein-protein interactions using ovine peptide-arrays: (i) sheep-PrP peptides 43–102, including the amino-terminal octarepeats, and (ii) sheep-PrP peptides 134–177 which encompasses most of the scrapie susceptibility-associated polymorphisms in sheep. Moroncini et al. <xref rid="pone.0041626-Moroncini1" ref-type="bibr">[55]</xref> found that residues within the 89–112 and 136–158 segments of PrP<sup>C</sup> are key components of the PrP<sup>C</sup>–PrP<sup>Sc</sup> complex. Beringue et al. <xref rid="pone.0041626-Beringue1" ref-type="bibr">[11]</xref> reported that antibodies exclusively binding PrP<sup>C</sup> were relatively inefficient inhibitors of PrP<sup>Sc</sup> accumulation compared with antibodies that additionally recognize disease-associated PrP isoforms. Féraudet et al. <xref rid="pone.0041626-Feraudet1" ref-type="bibr">[56]</xref> screened 145 anti-PrP Mabs for their capacity to inhibit PrP<sup>Sc</sup> replication in infected N2a or Rov9 cells. They identified four different linear epitopes that hindered the PrP<sup>C</sup> to PrP<sup>Sc</sup> conversion: the amino terminal region 26–35, the octarepeat region 59–89, the intermediate region 97–102, and the central region 130–160. The observation that antibodies that bind to the amino terminus of the prion protein are capable of inhibiting conversion suggests that the endogenous proteolytic cleavage occurs after the site of conversion.</p><p>To more completely explore the possible therapeutic effect of anti-PrP antibodies, and to establish another system to analyze the influence of Abs on the conversion process, we screened Mabs produced in our laboratory for their capacity to inhibit PrP<sup>Sc</sup> formation. This screening was performed using N2a/22L cells and cell-free sPMCA. In N2a/22L cultures, all Mabs that react with mouse PrP reduce PrP<sup>Sc</sup> formation although with varying efficiency. Thus, similar to previous results <xref rid="pone.0041626-Moroncini1" ref-type="bibr">[55]</xref>, we found that the ability to inhibit PrP<sup>C</sup> to PrP<sup>Sc</sup> conversion was not restricted to a single epitope or limited to a specific region of the protein. However, the greatest inhibition was observed with Mabs that targeted epitopes in the amino terminal, unstructured region of the PrP. The greatest inhibition in the N2a/22L cells was with Mab 5D6. This is consistent with a prior study using Mab 6D11 (anti-PrP residues 95–105) which in a screen of multiple Mabs, only one produced the greatest inhibition (∼100%) <xref rid="pone.0041626-Pankiewicz1" ref-type="bibr">[12]</xref>. Mab 6D11 has also been shown to have some efficacy <italic>in vivo</italic> prolonging the pre-symptomatic incubation period <xref rid="pone.0041626-Sadowski1" ref-type="bibr">[57]</xref>. The Mab inhibition results obtained using PMCA were similar to that found in the cell culture system. PMCA has the advantages over the cell culture model of being cost-effective, simple, rapid, sensitive, and more amenable to studies of dose dependence. For identification of potential candidate Mabs that might have <italic>in vivo</italic> activity it is likely that such Mabs would have to produce 90 to 100% inhibition in the much simpler <italic>in vitro</italic> systems.</p><p>The interaction of PrP<sup>C</sup> to PrP<sup>Sc</sup> is critically dependent on the structural compatibility of the molecules as supported by the existence of a species barrier for prion infection, related to minor differences in the primary sequence of PrP<sup>C</sup> in different species. Therefore, it is not surprising that antibodies that may alter or mask the critical epitopes on PrP<sup>C</sup> and/or PrP<sup>Sc</sup>, involved during the mutual conformational complementarity required in prion propagation, will be inhibitory for prion replication. Although many anti-PrP antibodies targeting different regions of PrP may have some therapeutic effect <italic>in vitro</italic>, it is not clear how this relates to their efficacy <italic>in vivo</italic>. On the one hand, it is tempting to speculate that only the antibodies exhibiting near complete inhibition <italic>in vitro</italic> would be effective <italic>in vivo</italic> given the obstacle of the blood brain barrier and access to PrP in cells. However, it is also possible that only partial inhibition of conversion is required <italic>in vivo</italic> allowing the cells to “recover”. In either case, it would be advantageous for these therapeutic antibodies to have high affinities of binding to PrP<sup>C</sup> and/or PrP<sup>Sc</sup>, as well as targeting specific critical PrP domains. One can hypothesize that the simultaneous targeting of more than one critical epitope will lead to greater benefits. However, co-treatment experiments performed with a mixture of two antibodies compatibly binding cell-surface PrP<sup>C</sup> did not show any benefit with compared to treatment involving a single Mab in our current experiments. In a previous study <xref rid="pone.0041626-Chang1" ref-type="bibr">[58]</xref>, we demonstrated synergistic binding with one of our antibody pairs. Synergistic binding of inhibitory Mabs, i.e. reaction with an antibody that increases the binding of the second antibody, would be predicted to enhance the inhibitory effect. Further studies with antibody pairs fitting this description will be required to test this hypothesis. 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