TY - JOUR
T1 - A Glimpse of Membrane Transport through Structures—Advances in the Structural Biology of the GLUT Glucose Transporters
AU - Yan, Nieng
N1 - Funding Information:
I thank Drs. Haipeng Gong and Haizong Shen for help with the manuscript preparation, and Dr. S. Frank Yan for critical reading of the manuscript. This work was supported by funds from the Ministry of Science and Technology of China (2015CB910101, 2016YFA0500402, 2014ZX09507003-006) and the National Natural Science Foundation of China (Project Nos. 31621092, 31630017, and 31611130036). Due to the page limit, the author apologizes to those whose outstanding work has not been cited or discussed in this review.
Publisher Copyright:
© 2017 Elsevier Ltd
PY - 2017/8/18
Y1 - 2017/8/18
N2 - The cellular uptake of glucose is an essential physiological process, and movement of glucose across biological membranes requires specialized transporters. The major facilitator superfamily glucose transporters GLUTs, encoded by the SLC2A genes, have been a paradigm for functional, mechanistic, and structural understanding of solute transport in the past century. This review starts with a glimpse into the structural biology of membrane proteins and particularly membrane transport proteins, enumerating the landmark structures in the past 25 years. The recent breakthrough in the structural elucidation of GLUTs is then elaborated following a brief overview of the research history of these archetypal transporters, their functional specificity, and physiological and pathophysiological significances. Structures of GLUT1, GLUT3, and GLUT5 in distinct transport and/or ligand-binding states reveal detailed mechanisms of the alternating access transport cycle and substrate recognition, and thus illuminate a path by which structure-based drug design may be applied to help discover novel therapeutics against several debilitating human diseases associated with GLUT malfunction and/or misregulation.
AB - The cellular uptake of glucose is an essential physiological process, and movement of glucose across biological membranes requires specialized transporters. The major facilitator superfamily glucose transporters GLUTs, encoded by the SLC2A genes, have been a paradigm for functional, mechanistic, and structural understanding of solute transport in the past century. This review starts with a glimpse into the structural biology of membrane proteins and particularly membrane transport proteins, enumerating the landmark structures in the past 25 years. The recent breakthrough in the structural elucidation of GLUTs is then elaborated following a brief overview of the research history of these archetypal transporters, their functional specificity, and physiological and pathophysiological significances. Structures of GLUT1, GLUT3, and GLUT5 in distinct transport and/or ligand-binding states reveal detailed mechanisms of the alternating access transport cycle and substrate recognition, and thus illuminate a path by which structure-based drug design may be applied to help discover novel therapeutics against several debilitating human diseases associated with GLUT malfunction and/or misregulation.
KW - GLUT1
KW - SLC2A
KW - alternating access
KW - major facilitator superfamily
KW - membrane transport
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U2 - 10.1016/j.jmb.2017.07.009
DO - 10.1016/j.jmb.2017.07.009
M3 - Review article
C2 - 28756087
AN - SCOPUS:85026528060
SN - 0022-2836
VL - 429
SP - 2710
EP - 2725
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 17
ER -