过剩3
过剩1
葡萄糖转运蛋白
结晶
重组DNA
运输机
配体(生物化学)
化学
结构生物学
计算生物学
生物化学
生物
受体
基因
有机化学
内分泌学
胰岛素
出处
期刊:Methods in molecular biology
日期:2017-12-07
卷期号:: 15-29
标识
DOI:10.1007/978-1-4939-7507-5_2
摘要
Overexpression, purification, and crystallization of eukaryotic membrane proteins represent a major challenge for structural biology. In recent years, we have solved the crystal structures of the human glucose transporters GLUT1 in the inward-open conformation at 3.17 Å resolution and GLUT3 in the outward-open and occluded conformations at 2.4 and 1.5 Å resolutions, respectively. Structural elucidation of these transporters in three distinct functional states reveal the molecular basis for the alternating access transport cycle of this prototypal solute carrier family. It established the molecular foundation for future dynamic and kinetic investigations of these GLUTs, and will likely facilitate structure-based ligand development. In this chapter, we present the detailed protocols of recombinant protein expression, purification, and crystallization of GLUT1 and GLUT3, which may help the pursuit of structural elucidation of other eukaryotic membrane proteins.
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