Publication: Biochemical characterization of detergent-resistant membranes: a systematic approach
cris.virtualsource.author-orcid | 083943e3-ae7a-4391-91d3-91bed86ab50e | |
cris.virtualsource.author-orcid | b4c31f46-29ab-4035-a115-1542a94c1d9a | |
datacite.rights | metadata.only | |
dc.contributor.author | Babiichuk, Eduard | |
dc.contributor.author | Draeger, Annette | |
dc.date.accessioned | 2024-10-13T13:34:50Z | |
dc.date.available | 2024-10-13T13:34:50Z | |
dc.date.issued | 2006 | |
dc.description.abstract | Lateral segregation of cholesterol- and sphingomyelin-rich rafts and glycerophospholipid-containing non-raft microdomains has been proposed to play a role in a variety of biological processes. The most compelling evidence for membrane segregation is based on the observation that extraction with non-ionic detergents leads to solubilization of a subset of membrane components only. However, one decade later, a large body of inconsistent detergent-extraction data is threatening the very concept of membrane segregation. We have assessed the validity of the existing paradigms and we show the following. (i) The localization of a membrane component within a particular fraction of a sucrose gradient cannot be taken as a yardstick for its solubility: a variable localization of the DRMs (detergent-resistant membranes) in sucrose gradients is the result of complex associations between the membrane skeleton and the lipid bilayer. (ii) DRMs of variable composition can be generated by using a single detergent, the increasing concentration of which gradually extracts one protein/lipid after another. Therefore any extraction pattern obtained by a single concentration experiment is bound to be 'investigator-specific'. It follows that comparison of DRMs obtained by different detergents in a single concentration experiment is prone to misinterpretations. (iii) Depletion of cholesterol has a graded effect on membrane solubility. (iv) Differences in detergent solubility of the members of the annexin protein family arise from their association with chemically different membrane compartments; however, these cannot be attributed to the 'brick-like' raft-building blocks of fixed size and chemical composition. Our findings demonstrate a need for critical re-evaluation of the accumulated detergent-extraction data. | |
dc.description.numberOfPages | 10 | |
dc.description.sponsorship | Institut für Anatomie, Zellbiologie | |
dc.description.sponsorship | Institut für Anatomie | |
dc.identifier.isi | 000239474100004 | |
dc.identifier.pmid | 16608442 | |
dc.identifier.publisherDOI | 10.1042/BJ20060056 | |
dc.identifier.uri | https://boris-portal.unibe.ch/handle/20.500.12422/92702 | |
dc.language.iso | en | |
dc.publisher | Portland Press | |
dc.publisher.place | London | |
dc.relation.isbn | 16608442 | |
dc.relation.ispartof | Biochemical journal | |
dc.relation.issn | 0264-6021 | |
dc.relation.organization | DCD5A442BD6DE17DE0405C82790C4DE2 | |
dc.relation.organization | DCD5A442BCD7E17DE0405C82790C4DE2 | |
dc.title | Biochemical characterization of detergent-resistant membranes: a systematic approach | |
dc.type | article | |
dspace.entity.type | Publication | |
oaire.citation.endPage | 16 | |
oaire.citation.issue | 3 | |
oaire.citation.startPage | 407 | |
oaire.citation.volume | 397 | |
oairecerif.author.affiliation | Institut für Anatomie, Zellbiologie | |
oairecerif.author.affiliation | Institut für Anatomie | |
unibe.contributor.role | creator | |
unibe.contributor.role | creator | |
unibe.description.ispublished | pub | |
unibe.eprints.legacyId | 18924 | |
unibe.journal.abbrevTitle | BIOCHEM J | |
unibe.subtype.article | journal |