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10.3389/fcell.2016.00035 http://scihub22266oqcxt.onion/10.3389/fcell.2016.00035 C4860415!4860415!27243003     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Front+Cell+Dev+Biol 2016 ; 4 (ä): ä Nephropedia Template TP {{tp|p=27243003|t=2016. Membrane Tethering Complexes in the Endosomal System |pdf=|usr=}}{{27243003}} gab.com Text Membrane Tethering Complexes in the Endosomal System JO: Front Cell Dev Biol http://www.kidney.de/pget.php?&tw=1&pmid=27243003 #FOAvip Vesicles that are generated by endocytic events at the plasma membrane are destined to early endosomes. A prerequisite for proper fusion is the tethering of two membrane entities. Tethering of vesicles to early endosomes is mediated by the class C core vacuole/endosome tethering (CORVET) complex, while fusion of late endosomes with lysosomes depends on the homotypic fusion and vacuole protein sorting (HOPS) complex. Recycling through the trans-Golgi network (TGN) and to the plasma membrane is facilitated by the Golgi associated retrograde protein (GARP) and endosome-associated recycling protein (EARP) complexes, respectively. However, there are other tethering functions in the endosomal system as there are multiple pathways through which proteins can be delivered from endosomes to either the TGN or the plasma membrane. Furthermore, proteins that may be part of novel tethering complexes have been recently identified. Thus, it is likely that more tethering factors exist. In this review, I will provide an overview of different tethering complexes of the endosomal system and discuss how they may provide specificity in membrane traffic. Twit Text FOAVip Membrane Tethering Complexes in the Endosomal System ????Front Cell Dev Biol http://www.kidney.de/pget.php?&tw=1&pmid=27243003 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27243003 #FOAvip English Wikipedia <ref>{{Cite pmid|27243003}}</ref> Membrane Tethering Complexes in the Endosomal System #MMPMID27243003 Spang A Front Cell Dev Biol 2016[]; 4 (ä): ä PMID27243003show ga Vesicles that are generated by endocytic events at the plasma membrane are destined to early endosomes. A prerequisite for proper fusion is the tethering of two membrane entities. Tethering of vesicles to early endosomes is mediated by the class C core vacuole/endosome tethering (CORVET) complex, while fusion of late endosomes with lysosomes depends on the homotypic fusion and vacuole protein sorting (HOPS) complex. Recycling through the trans-Golgi network (TGN) and to the plasma membrane is facilitated by the Golgi associated retrograde protein (GARP) and endosome-associated recycling protein (EARP) complexes, respectively. However, there are other tethering functions in the endosomal system as there are multiple pathways through which proteins can be delivered from endosomes to either the TGN or the plasma membrane. Furthermore, proteins that may be part of novel tethering complexes have been recently identified. Thus, it is likely that more tethering factors exist. In this review, I will provide an overview of different tethering complexes of the endosomal system and discuss how they may provide specificity in membrane traffic. äMembrane Tethering Complexes in the Endosomal System (epmc).pdf DeepDyve Pubget Overpricing