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SINGLE PARTICLE ANALYSIS AT HIGH RESOLUTION
被引:32
作者:

Cong, Yao
论文数: 0 引用数: 0
h-index: 0
机构:
Baylor Coll Med, Verna & Marrs McLean Dept Biochem & Mol Biol, Natl Ctr Macromol Imaging, Houston, TX 77030 USA Baylor Coll Med, Verna & Marrs McLean Dept Biochem & Mol Biol, Natl Ctr Macromol Imaging, Houston, TX 77030 USA

Ludtke, Steven J.
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h-index: 0
机构:
Baylor Coll Med, Verna & Marrs McLean Dept Biochem & Mol Biol, Natl Ctr Macromol Imaging, Houston, TX 77030 USA Baylor Coll Med, Verna & Marrs McLean Dept Biochem & Mol Biol, Natl Ctr Macromol Imaging, Houston, TX 77030 USA
机构:
[1] Baylor Coll Med, Verna & Marrs McLean Dept Biochem & Mol Biol, Natl Ctr Macromol Imaging, Houston, TX 77030 USA
来源:
METHODS IN ENZYMOLOGY, VOL 482: CRYO-EM, PART B: 3-D RECONSTRUCTION
|
2010年
/
482卷
关键词:
FATTY-ACID SYNTHASE;
ELECTRON CRYOMICROSCOPY;
CRYO-EM;
BIOLOGICAL MACROMOLECULES;
CRYOELECTRON MICROSCOPY;
NEW-GENERATION;
RECONSTRUCTION;
IMAGES;
REFINEMENT;
SUBUNIT;
D O I:
10.1016/S0076-6879(10)82009-9
中图分类号:
Q5 [生物化学];
学科分类号:
070307 [化学生物学];
摘要:
Electron cryomicroscopy (cryo-EM) and single particle analysis is emerging as a powerful technique for determining the 3D structure of large biomolecules and biomolecular assemblies in close to their native solution environment. Over the last decade, this technology has improved, first to sub-nanometer resolution, and more recently beyond 0.5 nm resolution. Achieving sub-nanometer resolution is now readily approachable on mid-range microscopes with straightforward data processing, so long as the target specimen meets some basic requirements. Achieving resolutions beyond 0.5 nm currently requires a high-end microscope and careful data acquisition and processing, with much more stringent specimen requirements. This chapter will review and discuss the methodologies for determining high-resolution cryo-EM structures of nonvirus particles to sub-nanometer resolution and beyond, with a particular focus on the reconstruction strategy implemented in the EMAN software suite.
引用
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页码:211 / 235
页数:25
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