TY - JOUR
T1 - Structure and mechanism in membrane trafficking
AU - Hughson, Frederick M.
AU - Reinisch, Karin M.
N1 - Funding Information:
We gratefully acknowledge Yiying Cai, Yi Ren, Scott Stagg, and Vinzenz Unger for providing figures. Work in our laboratories is funded by the National Institutes of Health ( GM071574 to F.M.H. and GM080616 to K.M.R.).
PY - 2010/8
Y1 - 2010/8
N2 - Cell biologists have long been interested in understanding the machinery that mediates movement of proteins and lipids between intracellular compartments. Much of this traffic is accomplished by vesicles (or other membranous carriers) that bud from one compartment and fuse with another. Given the pivotal roles that large protein complexes play in vesicular trafficking, many recent advances have relied on the combined use of X-ray crystallography and electron microscopy. Here, we discuss integrated structural studies of proteins whose assembly shapes membranes into vesicles and tubules, before turning to the so-called tethering factors that appear to orchestrate vesicle docking and fusion.
AB - Cell biologists have long been interested in understanding the machinery that mediates movement of proteins and lipids between intracellular compartments. Much of this traffic is accomplished by vesicles (or other membranous carriers) that bud from one compartment and fuse with another. Given the pivotal roles that large protein complexes play in vesicular trafficking, many recent advances have relied on the combined use of X-ray crystallography and electron microscopy. Here, we discuss integrated structural studies of proteins whose assembly shapes membranes into vesicles and tubules, before turning to the so-called tethering factors that appear to orchestrate vesicle docking and fusion.
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U2 - 10.1016/j.ceb.2010.03.011
DO - 10.1016/j.ceb.2010.03.011
M3 - Review article
C2 - 20418086
AN - SCOPUS:77955050491
SN - 0955-0674
VL - 22
SP - 454
EP - 460
JO - Current Opinion in Cell Biology
JF - Current Opinion in Cell Biology
IS - 4
ER -