ANALYSES OF SUBNANOMETER RESOLUTION CRYO-EM DENSITY MAPS

被引:16
作者
Baker, Matthew L. [1 ]
Baker, Mariah R. [1 ]
Hryc, Corey F. [1 ]
DiMaio, Frank [2 ]
机构
[1] Baylor Coll Med, Natl Ctr Macromol Imaging, Verna & Marrs McLean Dept Biochem & Mol Biol, Houston, TX 77030 USA
[2] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
来源
METHODS IN ENZYMOLOGY, VOL 483: CRYO-EM, PART C: ANALYSES, INTERPRETATION, AND CASE STUDIES | 2010年 / 483卷
关键词
PARTICLE ELECTRON CRYOMICROSCOPY; STRUCTURAL-INFORMATICS APPROACH; PROTEIN-STRUCTURE PREDICTION; X-RAY CRYSTALLOGRAPHY; FITTING ATOMIC MODELS; GROUP-II CHAPERONIN; RICE-DWARF-VIRUS; CRYOELECTRON MICROSCOPY; SECONDARY STRUCTURE; STRUCTURE REFINEMENT;
D O I
10.1016/S0076-6879(10)83001-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Today, electron cryomicroscopy (cryo-EM) can routinely achieve subnanometer resolutions of complex macromolecular assemblies. From a density map, one can extract key structural and functional information using a variety of computational analysis tools. At subnanometer resolution, these tools make it possible to isolate individual subunits, identify secondary structures, and accurately fit atomic models. With several cryo-EM studies achieving resolutions beyond 5 angstrom, computational modeling and feature recognition tools have been employed to construct backbone and atomic models of the protein components directly from a density map. In this chapter, we describe several common classes of computational tools that can be used to analyze and model subnanometer resolution reconstructions from cryo-EM. A general protocol for analyzing subnanometer resolution density maps is presented along with a full description of steps used in analyzing the 4.3 angstrom resolution structure of Mm-cpn.
引用
收藏
页码:1 / 29
页数:29
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