Literature DB >> 28756087

A Glimpse of Membrane Transport through Structures-Advances in the Structural Biology of the GLUT Glucose Transporters.

Nieng Yan1.   

Abstract

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 25years. 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.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  GLUT1; SLC2A; alternating access; major facilitator superfamily; membrane transport

Mesh:

Substances:

Year:  2017        PMID: 28756087     DOI: 10.1016/j.jmb.2017.07.009

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   5.469


  18 in total

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5.  Reconciling contradictory findings: Glucose transporter 1 (GLUT1) functions as an oligomer of allosteric, alternating access transporters.

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Journal:  J Biol Chem       Date:  2017-10-24       Impact factor: 5.157

6.  Extracellular gating of glucose transport through GLUT 1.

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Review 9.  Glucose transporters in adipose tissue, liver, and skeletal muscle in metabolic health and disease.

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10.  Screening of candidate substrates and coupling ions of transporters by thermostability shift assays.

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