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  • 1
    Publication Date: 2014-07-26
    Description: Clathrin-mediated endocytosis (CME) is vital for the internalization of most cell-surface proteins. In CME, plasma membrane-binding clathrin adaptors recruit and polymerize clathrin to form clathrin-coated pits into which cargo is sorted. Assembly polypeptide 2 (AP2) is the most abundant adaptor and is pivotal to CME. Here, we determined a structure of AP2 that includes the clathrin-binding beta2 hinge and developed an AP2-dependent budding assay. Our findings suggest that an autoinhibitory mechanism prevents clathrin recruitment by cytosolic AP2. A large-scale conformational change driven by the plasma membrane phosphoinositide phosphatidylinositol 4,5-bisphosphate and cargo relieves this autoinhibition, triggering clathrin recruitment and hence clathrin-coated bud formation. This molecular switching mechanism can couple AP2's membrane recruitment to its key functions of cargo and clathrin binding.〈br /〉〈br /〉〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333214/" target="_blank"〉〈img src="https://static.pubmed.gov/portal/portal3rc.fcgi/4089621/img/3977009" border="0"〉〈/a〉   〈a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4333214/" target="_blank"〉This paper as free author manuscript - peer-reviewed and accepted for publication〈/a〉〈br /〉〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Kelly, Bernard T -- Graham, Stephen C -- Liska, Nicole -- Dannhauser, Philip N -- Honing, Stefan -- Ungewickell, Ernst J -- Owen, David J -- 079895/Wellcome Trust/United Kingdom -- 090909/Wellcome Trust/United Kingdom -- 090909/Z/09/Z/Wellcome Trust/United Kingdom -- 098406/Wellcome Trust/United Kingdom -- 098406/Z/12/Z/Wellcome Trust/United Kingdom -- 100140/Wellcome Trust/United Kingdom -- New York, N.Y. -- Science. 2014 Jul 25;345(6195):459-63. doi: 10.1126/science.1254836.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Cambridge Institute for Medical Research (CIMR), Department of Clinical Biochemistry, University of Cambridge, Hills Road, Cambridge CB2 0XY, UK. btk1000@cam.ac.uk djo30@cam.ac.uk. ; Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK. ; Cambridge Institute for Medical Research (CIMR), Department of Clinical Biochemistry, University of Cambridge, Hills Road, Cambridge CB2 0XY, UK. ; Department of Cell Biology, Center of Anatomy, Hannover Medical School, Carl-Neuberg Strasse 1, D-30625 Hannover, Germany. ; Institute of Biochemistry I and Center for Molecular Medicine Cologne, University of Cologne, Joseph-Stelzmann-Strasse 52, 50931 Cologne, Germany.〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/25061211" target="_blank"〉PubMed〈/a〉
    Keywords: Adaptor Protein Complex 2/*chemistry ; Adaptor Protein Complex beta Subunits/*chemistry ; Cell Membrane/*chemistry ; Clathrin/*chemistry ; Endocytosis ; Humans ; Phosphatidylinositol 4,5-Diphosphate/chemistry ; *Polymerization
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 2
    Publication Date: 2011-05-18
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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  • 3
    Publication Date: 2011-06-08
    Description: Growing knowledge of the key molecular components involved in biological processes such as endocytosis, exocytosis, and motility has enabled direct testing of proposed mechanistic models by reconstitution. However, current techniques for building increasingly complex cellular structures and functions from purified components are limited in their ability to create conditions that emulate the physical and biochemical constraints of real cells. Here we present an integrated method for forming giant unilamellar vesicles with simultaneous control over (i) lipid composition and asymmetry, (ii) oriented membrane protein incorporation, and (iii) internal contents. As an application of this method, we constructed a synthetic system in which membrane proteins were delivered to the outside of giant vesicles, mimicking aspects of exocytosis. Using confocal fluorescence microscopy, we visualized small encapsulated vesicles docking and mixing membrane components with the giant vesicle membrane, resulting in exposure of previously encapsulated membrane proteins to the external environment. This method for creating giant vesicles can be used to test models of biological processes that depend on confined volume and complex membrane composition, and it may be useful in constructing functional systems for therapeutic and biomaterials applications.
    Print ISSN: 0027-8424
    Electronic ISSN: 1091-6490
    Topics: Biology , Medicine , Natural Sciences in General
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