Kinetic and thermodynamic analysis of the interaction between TRAP (trp RNA-binding attenuation protein) of Bacillus subtilis and trp leader RNA.
Identifieur interne : 003E22 ( Main/Curation ); précédent : 003E21; suivant : 003E23Kinetic and thermodynamic analysis of the interaction between TRAP (trp RNA-binding attenuation protein) of Bacillus subtilis and trp leader RNA.
Auteurs : C. Baumann [États-Unis] ; J. Otridge ; P. GollnickSource :
- The Journal of biological chemistry [ 0021-9258 ] ; 1996.
Descripteurs français
- KwdFr :
- ARN messager (), Amorces ADN, Bacillus subtilis (), Cinétique, Concentration en ions d'hydrogène, Données de séquences moléculaires, Facteurs de transcription (), Facteurs de transcription (génétique), Facteurs de transcription (métabolisme), Liaison aux protéines, Protéines bactériennes, Protéines de liaison à l'ARN (), Protéines de liaison à l'ARN (génétique), Protéines de liaison à l'ARN (métabolisme), Sels, Séquence nucléotidique, Thermodynamique, Tryptophane ().
- MESH :
- génétique : Facteurs de transcription, Protéines de liaison à l'ARN.
- métabolisme : Facteurs de transcription, Protéines de liaison à l'ARN.
- ARN messager, Amorces ADN, Bacillus subtilis, Cinétique, Concentration en ions d'hydrogène, Données de séquences moléculaires, Facteurs de transcription, Liaison aux protéines, Protéines bactériennes, Protéines de liaison à l'ARN, Sels, Séquence nucléotidique, Thermodynamique, Tryptophane.
English descriptors
- KwdEn :
- Bacillus subtilis (chemistry), Bacterial Proteins, Base Sequence, DNA Primers, Hydrogen-Ion Concentration, Kinetics, Molecular Sequence Data, Protein Binding, RNA, Messenger (chemistry), RNA-Binding Proteins (chemistry), RNA-Binding Proteins (genetics), RNA-Binding Proteins (metabolism), Salts, Thermodynamics, Transcription Factors (chemistry), Transcription Factors (genetics), Transcription Factors (metabolism), Tryptophan (chemistry).
- MESH :
- chemical , chemistry : RNA, Messenger, RNA-Binding Proteins, Transcription Factors, Tryptophan.
- chemical , genetics : RNA-Binding Proteins, Transcription Factors.
- chemical , metabolism : RNA-Binding Proteins, Transcription Factors.
- chemical : Bacterial Proteins, DNA Primers, Salts.
- chemistry : Bacillus subtilis.
- Base Sequence, Hydrogen-Ion Concentration, Kinetics, Molecular Sequence Data, Protein Binding, Thermodynamics.
Abstract
In Bacillus subtilis, expression of the tryptophan biosynthetic genes is regulated in response to tryptophan by an RNA-binding protein called TRAP (trp RNA-binding attenuation protein). TRAP has been shown to contain 11 identical subunits arranged in a symmetrical ring. Kinetic and thermodynamic parameters of the interaction between tryptophan-activated TRAP and trp leader RNA were studied. Results from glycerol gradients and mobility shift gels indicate that two TRAP 11-mers bind to each trp leader RNA. A filter binding assay was used to determine an apparent binding constant of 8.0 +/- 1.3 x 10(9) m-1 (Kd = 0.12 +/- 0.02 nM) for TRAP and an RNA containing residues +36 to +92 of the trp leader RNA in 1 mM L-tryptophan at 37 degrees C. The temperature dependence of Kapp was somewhat unexpected demonstrating that the delta H of the interaction is highly unfavorable at + 15.9 kcal mol-1. Therefore, the interaction is completely driven by a delta S of +97 cal mol-1 K-1. The interaction between tryptophan-activated TRAP and trp leader RNA displayed broad salt and pH activity profiles. Finally, the rate of RNA dissociation from the RNA-TRAP.tryptophan ternary complex was found to be very slow in high concentrations of tryptophan (> 40 microM) but increased in lower tryptophan concentrations. This suggests that dissociation of tryptophan from the ternary complex is the rate-limiting step in RNA dissociation.
DOI: 10.1074/jbc.271.21.12269
PubMed: 8647825
Links toward previous steps (curation, corpus...)
- to stream PubMed, to step Corpus: Pour aller vers cette notice dans l'étape Curation :002774
- to stream PubMed, to step Curation: Pour aller vers cette notice dans l'étape Curation :002774
- to stream PubMed, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :002623
- to stream Ncbi, to step Merge: Pour aller vers cette notice dans l'étape Curation :002A19
- to stream Ncbi, to step Curation: Pour aller vers cette notice dans l'étape Curation :002A19
- to stream Ncbi, to step Checkpoint: Pour aller vers cette notice dans l'étape Curation :002A19
- to stream Main, to step Merge: Pour aller vers cette notice dans l'étape Curation :003E77
Links to Exploration step
pubmed:8647825Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Kinetic and thermodynamic analysis of the interaction between TRAP (trp RNA-binding attenuation protein) of Bacillus subtilis and trp leader RNA.</title>
<author><name sortKey="Baumann, C" sort="Baumann, C" uniqKey="Baumann C" first="C" last="Baumann">C. Baumann</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Biological Sciences, State University of New York at Buffalo 14260, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Biological Sciences, State University of New York at Buffalo 14260</wicri:regionArea>
<wicri:noRegion>State University of New York at Buffalo 14260</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Otridge, J" sort="Otridge, J" uniqKey="Otridge J" first="J" last="Otridge">J. Otridge</name>
</author>
<author><name sortKey="Gollnick, P" sort="Gollnick, P" uniqKey="Gollnick P" first="P" last="Gollnick">P. Gollnick</name>
</author>
</titleStmt>
<publicationStmt><idno type="wicri:source">PubMed</idno>
<date when="1996">1996</date>
<idno type="RBID">pubmed:8647825</idno>
<idno type="pmid">8647825</idno>
<idno type="doi">10.1074/jbc.271.21.12269</idno>
<idno type="wicri:Area/PubMed/Corpus">002774</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Corpus" wicri:corpus="PubMed">002774</idno>
<idno type="wicri:Area/PubMed/Curation">002774</idno>
<idno type="wicri:explorRef" wicri:stream="PubMed" wicri:step="Curation">002774</idno>
<idno type="wicri:Area/PubMed/Checkpoint">002623</idno>
<idno type="wicri:explorRef" wicri:stream="Checkpoint" wicri:step="PubMed">002623</idno>
<idno type="wicri:Area/Ncbi/Merge">002A19</idno>
<idno type="wicri:Area/Ncbi/Curation">002A19</idno>
<idno type="wicri:Area/Ncbi/Checkpoint">002A19</idno>
<idno type="wicri:doubleKey">0021-9258:1996:Baumann C:kinetic:and:thermodynamic</idno>
<idno type="wicri:Area/Main/Merge">003E77</idno>
<idno type="wicri:Area/Main/Curation">003E22</idno>
</publicationStmt>
<sourceDesc><biblStruct><analytic><title xml:lang="en">Kinetic and thermodynamic analysis of the interaction between TRAP (trp RNA-binding attenuation protein) of Bacillus subtilis and trp leader RNA.</title>
<author><name sortKey="Baumann, C" sort="Baumann, C" uniqKey="Baumann C" first="C" last="Baumann">C. Baumann</name>
<affiliation wicri:level="1"><nlm:affiliation>Department of Biological Sciences, State University of New York at Buffalo 14260, USA.</nlm:affiliation>
<country xml:lang="fr">États-Unis</country>
<wicri:regionArea>Department of Biological Sciences, State University of New York at Buffalo 14260</wicri:regionArea>
<wicri:noRegion>State University of New York at Buffalo 14260</wicri:noRegion>
</affiliation>
</author>
<author><name sortKey="Otridge, J" sort="Otridge, J" uniqKey="Otridge J" first="J" last="Otridge">J. Otridge</name>
</author>
<author><name sortKey="Gollnick, P" sort="Gollnick, P" uniqKey="Gollnick P" first="P" last="Gollnick">P. Gollnick</name>
</author>
</analytic>
<series><title level="j">The Journal of biological chemistry</title>
<idno type="ISSN">0021-9258</idno>
<imprint><date when="1996" type="published">1996</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc><textClass><keywords scheme="KwdEn" xml:lang="en"><term>Bacillus subtilis (chemistry)</term>
<term>Bacterial Proteins</term>
<term>Base Sequence</term>
<term>DNA Primers</term>
<term>Hydrogen-Ion Concentration</term>
<term>Kinetics</term>
<term>Molecular Sequence Data</term>
<term>Protein Binding</term>
<term>RNA, Messenger (chemistry)</term>
<term>RNA-Binding Proteins (chemistry)</term>
<term>RNA-Binding Proteins (genetics)</term>
<term>RNA-Binding Proteins (metabolism)</term>
<term>Salts</term>
<term>Thermodynamics</term>
<term>Transcription Factors (chemistry)</term>
<term>Transcription Factors (genetics)</term>
<term>Transcription Factors (metabolism)</term>
<term>Tryptophan (chemistry)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>ARN messager ()</term>
<term>Amorces ADN</term>
<term>Bacillus subtilis ()</term>
<term>Cinétique</term>
<term>Concentration en ions d'hydrogène</term>
<term>Données de séquences moléculaires</term>
<term>Facteurs de transcription ()</term>
<term>Facteurs de transcription (génétique)</term>
<term>Facteurs de transcription (métabolisme)</term>
<term>Liaison aux protéines</term>
<term>Protéines bactériennes</term>
<term>Protéines de liaison à l'ARN ()</term>
<term>Protéines de liaison à l'ARN (génétique)</term>
<term>Protéines de liaison à l'ARN (métabolisme)</term>
<term>Sels</term>
<term>Séquence nucléotidique</term>
<term>Thermodynamique</term>
<term>Tryptophane ()</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en"><term>RNA, Messenger</term>
<term>RNA-Binding Proteins</term>
<term>Transcription Factors</term>
<term>Tryptophan</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>RNA-Binding Proteins</term>
<term>Transcription Factors</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>RNA-Binding Proteins</term>
<term>Transcription Factors</term>
</keywords>
<keywords scheme="MESH" type="chemical" xml:lang="en"><term>Bacterial Proteins</term>
<term>DNA Primers</term>
<term>Salts</term>
</keywords>
<keywords scheme="MESH" qualifier="chemistry" xml:lang="en"><term>Bacillus subtilis</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Facteurs de transcription</term>
<term>Protéines de liaison à l'ARN</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Facteurs de transcription</term>
<term>Protéines de liaison à l'ARN</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Base Sequence</term>
<term>Hydrogen-Ion Concentration</term>
<term>Kinetics</term>
<term>Molecular Sequence Data</term>
<term>Protein Binding</term>
<term>Thermodynamics</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>ARN messager</term>
<term>Amorces ADN</term>
<term>Bacillus subtilis</term>
<term>Cinétique</term>
<term>Concentration en ions d'hydrogène</term>
<term>Données de séquences moléculaires</term>
<term>Facteurs de transcription</term>
<term>Liaison aux protéines</term>
<term>Protéines bactériennes</term>
<term>Protéines de liaison à l'ARN</term>
<term>Sels</term>
<term>Séquence nucléotidique</term>
<term>Thermodynamique</term>
<term>Tryptophane</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front><div type="abstract" xml:lang="en">In Bacillus subtilis, expression of the tryptophan biosynthetic genes is regulated in response to tryptophan by an RNA-binding protein called TRAP (trp RNA-binding attenuation protein). TRAP has been shown to contain 11 identical subunits arranged in a symmetrical ring. Kinetic and thermodynamic parameters of the interaction between tryptophan-activated TRAP and trp leader RNA were studied. Results from glycerol gradients and mobility shift gels indicate that two TRAP 11-mers bind to each trp leader RNA. A filter binding assay was used to determine an apparent binding constant of 8.0 +/- 1.3 x 10(9) m-1 (Kd = 0.12 +/- 0.02 nM) for TRAP and an RNA containing residues +36 to +92 of the trp leader RNA in 1 mM L-tryptophan at 37 degrees C. The temperature dependence of Kapp was somewhat unexpected demonstrating that the delta H of the interaction is highly unfavorable at + 15.9 kcal mol-1. Therefore, the interaction is completely driven by a delta S of +97 cal mol-1 K-1. The interaction between tryptophan-activated TRAP and trp leader RNA displayed broad salt and pH activity profiles. Finally, the rate of RNA dissociation from the RNA-TRAP.tryptophan ternary complex was found to be very slow in high concentrations of tryptophan (> 40 microM) but increased in lower tryptophan concentrations. This suggests that dissociation of tryptophan from the ternary complex is the rate-limiting step in RNA dissociation.</div>
</front>
</TEI>
</record>
Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Sante/explor/MersV1/Data/Main/Curation
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 003E22 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Main/Curation/biblio.hfd -nk 003E22 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien |wiki= Sante |area= MersV1 |flux= Main |étape= Curation |type= RBID |clé= pubmed:8647825 |texte= Kinetic and thermodynamic analysis of the interaction between TRAP (trp RNA-binding attenuation protein) of Bacillus subtilis and trp leader RNA. }}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Curation/RBID.i -Sk "pubmed:8647825" \ | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Curation/biblio.hfd \ | NlmPubMed2Wicri -a MersV1
![]() | This area was generated with Dilib version V0.6.33. | ![]() |