Validity and applicability of membrane model systems for studying interactions of peripheral membrane proteins with lipids.
Identifieur interne : 000285 ( Main/Exploration ); précédent : 000284; suivant : 000286Validity and applicability of membrane model systems for studying interactions of peripheral membrane proteins with lipids.
Auteurs : RBID : pubmed:24374254Abstract
The cell membrane serves, at the same time, both as a barrier that segregates as well as a functional layer that facilitates selective communication. It is characterized as much by the complexity of its components as by the myriad of signaling process that it supports. And, herein lays the problems in its study and understanding of its behavior - it has a complex and dynamic nature that is further entangled by the fact that many events are both temporal and transient in their nature. Model membrane systems that bypass cellular complexity and compositional diversity have tremendously accelerated our understanding of the mechanisms and biological consequences of lipid-lipid and protein-lipid interactions. Concurrently, in some cases, the validity and applicability of model membrane systems are tarnished by inherent methodical limitations as well as undefined quality criteria. In this review we introduce membrane model systems widely used to study protein-lipid interactions in the context of key parameters of the membrane that govern lipid availability for peripheral membrane proteins. This article is part of a Special Issue entitled Tools to study lipid functions.
DOI: 10.1016/j.bbalip.2013.12.012
PubMed: 24374254
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<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Validity and applicability of membrane model systems for studying interactions of peripheral membrane proteins with lipids.</title><author><name sortKey="Czogalla, Aleksander" uniqKey="Czogalla A">Aleksander Czogalla</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD), Germany. Electronic address: czogalla@plid.de.</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD)</wicri:regionArea><wicri:noRegion>Germany; German Center for Diabetes Research (DZD)</wicri:noRegion></affiliation></author><author><name sortKey="Grzybek, Micha" uniqKey="Grzybek M">Michał Grzybek</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD), Germany.</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD)</wicri:regionArea><wicri:noRegion>Germany; German Center for Diabetes Research (DZD)</wicri:noRegion></affiliation></author><author><name sortKey="Jones, Walis" uniqKey="Jones W">Walis Jones</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD), Germany.</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD)</wicri:regionArea><wicri:noRegion>Germany; German Center for Diabetes Research (DZD)</wicri:noRegion></affiliation></author><author><name sortKey="Coskun, Unal" uniqKey="Coskun U">Unal Coskun</name><affiliation wicri:level="1"><nlm:affiliation>Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD), Germany. Electronic address: coskun@plid.de.</nlm:affiliation><country xml:lang="fr">Allemagne</country><wicri:regionArea>Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD)</wicri:regionArea><wicri:noRegion>Germany; German Center for Diabetes Research (DZD)</wicri:noRegion></affiliation></author></titleStmt><publicationStmt><date when="2013">2013</date><idno type="RBID">pubmed:24374254</idno><idno type="pmid">24374254</idno><idno type="doi">10.1016/j.bbalip.2013.12.012</idno><idno type="wicri:Area/Main/Corpus">000233</idno><idno type="wicri:Area/Main/Curation">000233</idno><idno type="wicri:Area/Main/Exploration">000285</idno></publicationStmt></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">The cell membrane serves, at the same time, both as a barrier that segregates as well as a functional layer that facilitates selective communication. It is characterized as much by the complexity of its components as by the myriad of signaling process that it supports. And, herein lays the problems in its study and understanding of its behavior - it has a complex and dynamic nature that is further entangled by the fact that many events are both temporal and transient in their nature. Model membrane systems that bypass cellular complexity and compositional diversity have tremendously accelerated our understanding of the mechanisms and biological consequences of lipid-lipid and protein-lipid interactions. Concurrently, in some cases, the validity and applicability of model membrane systems are tarnished by inherent methodical limitations as well as undefined quality criteria. In this review we introduce membrane model systems widely used to study protein-lipid interactions in the context of key parameters of the membrane that govern lipid availability for peripheral membrane proteins. This article is part of a Special Issue entitled Tools to study lipid functions.</div></front></TEI><pubmed><MedlineCitation Status="Publisher" Owner="NLM"><PMID Version="1">24374254</PMID><DateCreated><Year>2014</Year><Month>1</Month><Day>15</Day></DateCreated><Article PubModel="Print-Electronic"><Journal><ISSN IssnType="Print">0006-3002</ISSN><JournalIssue CitedMedium="Print"><PubDate><Year>2013</Year><Month>Dec</Month><Day>27</Day></PubDate></JournalIssue><Title>Biochimica et biophysica acta</Title><ISOAbbreviation>Biochim. Biophys. Acta</ISOAbbreviation></Journal><ArticleTitle>Validity and applicability of membrane model systems for studying interactions of peripheral membrane proteins with lipids.</ArticleTitle><Pagination><MedlinePgn></MedlinePgn></Pagination><ELocationID EIdType="pii">S1388-1981(13)00285-0</ELocationID><ELocationID EIdType="doi">10.1016/j.bbalip.2013.12.012</ELocationID><Abstract><AbstractText NlmCategory="UNLABELLED">The cell membrane serves, at the same time, both as a barrier that segregates as well as a functional layer that facilitates selective communication. It is characterized as much by the complexity of its components as by the myriad of signaling process that it supports. And, herein lays the problems in its study and understanding of its behavior - it has a complex and dynamic nature that is further entangled by the fact that many events are both temporal and transient in their nature. Model membrane systems that bypass cellular complexity and compositional diversity have tremendously accelerated our understanding of the mechanisms and biological consequences of lipid-lipid and protein-lipid interactions. Concurrently, in some cases, the validity and applicability of model membrane systems are tarnished by inherent methodical limitations as well as undefined quality criteria. In this review we introduce membrane model systems widely used to study protein-lipid interactions in the context of key parameters of the membrane that govern lipid availability for peripheral membrane proteins. This article is part of a Special Issue entitled Tools to study lipid functions.</AbstractText><CopyrightInformation>Copyright © 2013 Elsevier B.V. All rights reserved.</CopyrightInformation></Abstract><AuthorList><Author><LastName>Czogalla</LastName><ForeName>Aleksander</ForeName><Initials>A</Initials><Affiliation>Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD), Germany. Electronic address: czogalla@plid.de.</Affiliation></Author><Author><LastName>Grzybek</LastName><ForeName>Michał</ForeName><Initials>M</Initials><Affiliation>Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD), Germany.</Affiliation></Author><Author><LastName>Jones</LastName><ForeName>Walis</ForeName><Initials>W</Initials><Affiliation>Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD), Germany.</Affiliation></Author><Author><LastName>Coskun</LastName><ForeName>Unal</ForeName><Initials>U</Initials><Affiliation>Laboratory of Membrane Biochemistry, Paul Langerhans Institute Dresden, Faculty of Medicine Carl Gustav Carus at the TU Dresden, Fetscherstrasse 74, 01307 Dresden, Germany; German Center for Diabetes Research (DZD), Germany. 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