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10.1038/nrm.2016.121 http://scihub22266oqcxt.onion/10.1038/nrm.2016.121 C5198518!5198518!27703243     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27703243&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Nat+Rev+Mol+Cell+Biol 2017 ; 18 (1): 5-17 Nephropedia Template TP {{tp|p=27703243|t=2017. Reverse-topology membrane scission by the ESCRT complexes |pdf=|usr=}}{{27703243}} gab.com Text Reverse-topology membrane scission by the ESCRT complexes JO: Nat Rev Mol Cell Biol http://www.kidney.de/pget.php?&tw=1&pmid=27703243 #FOAvip The narrow membrane necks formed during viral, exosomal, and intra-endosomal budding from membranes, cytokinesis, and related processes have interiors that are contiguous with the cytosol. The severing of these necks involves action from the opposite face of the membrane as compared to the well-characterized coated vesicle pathways, and is referred to as ?reverse? or ?inverse? topology membrane scission. This process is carried out by the endosomal sorting complexes required for transport (ESCRT) proteins. In particular, the ESCRT-III proteins can form filaments, flat spirals, tubes and conical funnels, which are thought to somehow direct membrane remodeling and scission. Their assembly, and their disassembly by the ATPase VPS4, has been intensively studied, but the mechanism of scission has been elusive. New insights from cryo-electron microscopy and various types of spectroscopy may finally be close to rectifying this situation. Twit Text FOAVip Reverse-topology membrane scission by the ESCRT complexes ????Nat Rev Mol Cell Biol http://www.kidney.de/pget.php?&tw=1&pmid=27703243 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27703243 #FOAvip English Wikipedia <ref>{{Cite pmid|27703243}}</ref> Reverse-topology membrane scission by the ESCRT complexes #MMPMID27703243 Schöneberg J; Lee IH; Iwasa JH; Hurley JH Nat Rev Mol Cell Biol 2017[Jan]; 18 (1): 5-17 PMID27703243show ga The narrow membrane necks formed during viral, exosomal, and intra-endosomal budding from membranes, cytokinesis, and related processes have interiors that are contiguous with the cytosol. The severing of these necks involves action from the opposite face of the membrane as compared to the well-characterized coated vesicle pathways, and is referred to as ?reverse? or ?inverse? topology membrane scission. This process is carried out by the endosomal sorting complexes required for transport (ESCRT) proteins. In particular, the ESCRT-III proteins can form filaments, flat spirals, tubes and conical funnels, which are thought to somehow direct membrane remodeling and scission. Their assembly, and their disassembly by the ATPase VPS4, has been intensively studied, but the mechanism of scission has been elusive. New insights from cryo-electron microscopy and various types of spectroscopy may finally be close to rectifying this situation. äReverse-topology membrane scission by the ESCRT complexes (epmc).pdf DeepDyve Pubget Overpricing