Single-particle Cryo-EM of calcium release channels: structural validation

被引:18
作者
Ludtke, Steven J. [1 ]
Serysheva, Irina I. [2 ]
机构
[1] Baylor Coll Med, Verna & Marrs McLean Dept Biochem & Mol Biol, Natl Ctr Macromol Imaging, Houston, TX 77030 USA
[2] Univ Texas Med Sch Houston, Dept Biochem & Mol Biol, Struct Biol Imaging Ctr, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR; NICOTINIC ACETYLCHOLINE-RECEPTOR; MUSCLE SARCOPLASMIC-RETICULUM; RYANODINE RECEPTOR; ELECTRON CRYOMICROSCOPY; CRYSTAL-STRUCTURES; TRANSMEMBRANE DOMAINS; BINDING; MICROSCOPY; RESOLUTION;
D O I
10.1016/j.sbi.2013.06.003
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Few tools are available to determine the structure of large integral membrane proteins such as intracellular Ca2+ release channels, RyRs and IP(3)Rs. Single particle cryo-EM can readily determine the structure of such channels to intermediate resolution, and can be used to quantitatively assess conformational variability. However, due to the, often low, image contrast of these cryospecimens, methods for validation are critical to insure the accuracy of such structures, and to put limits on their interpretability. The low-resolution structure of RyR has been well established for some time, but high-resolution has been slow to emerge. The structure of IP3R channel by cryo-EM had a number of false-starts, but improved validation methods have recently lead to a demonstrably accurate reconstruction.
引用
收藏
页码:755 / 762
页数:8
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