Validation of Cryo-EM Structure of IP3R1 Channel

被引:37
作者
Murray, Stephen C. [1 ,2 ]
Flanagan, John [2 ]
Popova, Olga B. [3 ]
Chiu, Wah [1 ,2 ]
Ludtke, Steven J. [1 ,2 ]
Serysheva, Irina I. [2 ,3 ]
机构
[1] Baylor Coll Med, Grad Program Struct & Computat Biol & Mol Biophys, Houston, TX 77030 USA
[2] Baylor Coll Med, Natl Ctr Macromol Imaging, Verna & Marrs McLean Dept Biochem & Mol Biol, Houston, TX 77030 USA
[3] Univ Texas Med Sch Houston, Dept Biochem & Mol Biol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
INOSITOL 1,4,5-TRISPHOSPHATE RECEPTOR; ELECTRON CRYOMICROSCOPY; GROEL; MICROSCOPY; RESOLUTION; ORIENTATION; REFINEMENT; BINDING;
D O I
10.1016/j.str.2013.04.016
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
About a decade ago, three electron cryomicroscopy (cryo-EM) single-particle reconstructions of IP(3)R1 were reported at low resolution. It was disturbing that these structures bore little similarity to one another, even at the level of quaternary structure. Recently, we published an improved structure of IP(3)R1 at similar to 1 nm resolution. However, this structure did not bear any resemblance to any of the three previously published structures, leading to the question of why the structure should be considered more reliable than the original three. Here, we apply several methods, including class-average/map comparisons, tilt-pair validation, and use of multiple refinement software packages, to give strong evidence for the reliability of our recent structure. The map resolution and feature resolvability are assessed with the gold standard criterion. This approach is generally applicable to assessing the validity of cryo-EM maps of other molecular machines.
引用
收藏
页码:900 / 909
页数:10
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