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Mechanism of spontaneous inside-out vesiculation of red cell membranes

In certain conditions, human red cell membranes spontaneously form inside out vesicles within 20 min after hypotonic lysis. Study of the geometry of this process now reveals that, contrary to earlier views of vesiculation by endocytosis or by the mechanical shearing of cytoskeleton-depleted membrane...

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Detalles Bibliográficos
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2115135/
https://www.ncbi.nlm.nih.gov/pubmed/3384849
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description In certain conditions, human red cell membranes spontaneously form inside out vesicles within 20 min after hypotonic lysis. Study of the geometry of this process now reveals that, contrary to earlier views of vesiculation by endocytosis or by the mechanical shearing of cytoskeleton-depleted membrane, lysis generates a persistent membrane edge which spontaneously curls, cuts, and splices the membrane surface to form single or concentric vesicles. Analysis of the processes by which proteins may stabilize a free membrane edge led us to formulate a novel zip-type mechanism for membrane cutting-splicing and fusion even in the absence of free edges. Such protein-led membrane fusion represents an alternative to mechanisms of membrane fusion based on phospholipid interactions, and may prove relevant to processes of secretion, endocytosis, phagocytosis, and membrane recycling in many cell types.
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spelling pubmed-21151352008-05-01 Mechanism of spontaneous inside-out vesiculation of red cell membranes J Cell Biol Articles In certain conditions, human red cell membranes spontaneously form inside out vesicles within 20 min after hypotonic lysis. Study of the geometry of this process now reveals that, contrary to earlier views of vesiculation by endocytosis or by the mechanical shearing of cytoskeleton-depleted membrane, lysis generates a persistent membrane edge which spontaneously curls, cuts, and splices the membrane surface to form single or concentric vesicles. Analysis of the processes by which proteins may stabilize a free membrane edge led us to formulate a novel zip-type mechanism for membrane cutting-splicing and fusion even in the absence of free edges. Such protein-led membrane fusion represents an alternative to mechanisms of membrane fusion based on phospholipid interactions, and may prove relevant to processes of secretion, endocytosis, phagocytosis, and membrane recycling in many cell types. The Rockefeller University Press 1988-06-01 /pmc/articles/PMC2115135/ /pubmed/3384849 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
Mechanism of spontaneous inside-out vesiculation of red cell membranes
title Mechanism of spontaneous inside-out vesiculation of red cell membranes
title_full Mechanism of spontaneous inside-out vesiculation of red cell membranes
title_fullStr Mechanism of spontaneous inside-out vesiculation of red cell membranes
title_full_unstemmed Mechanism of spontaneous inside-out vesiculation of red cell membranes
title_short Mechanism of spontaneous inside-out vesiculation of red cell membranes
title_sort mechanism of spontaneous inside-out vesiculation of red cell membranes
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2115135/
https://www.ncbi.nlm.nih.gov/pubmed/3384849