A strategy for electron tomographic data collection and crystallographic reconstruction of biological bundles

被引:9
作者
Sherman, MB [1 ]
Jakana, J
Sun, SJ
Matsudaira, P
Chiu, W
Schmid, MF
机构
[1] Natl Ctr Macromol Imaging, Houston, TX 77030 USA
[2] Baylor Coll Med, Verna & Marrs Mclean Dept Biochem, Houston, TX 77030 USA
[3] MIT, Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[4] MIT, Dept Biol, Cambridge, MA 02142 USA
关键词
acrosomal bundles; actin; scruin; electron crystallography; tomography; electron cryomicroscopy; tilt series imaging; profile fitting;
D O I
10.1006/jsbi.1997.3916
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
Structures of highly ordered biological bundles have unique features which call for special experimental and computational methods in electron cryomicroscopy. They can be considered as three dimensional quasi-crystals and reconstructed using a crystallographic approach. However, they are neither "infinitely" large with respect to the borders of the bundle, nor are they a single unit cell in thickness along the viewing direction, Also, because of their shape, bundles do not generally have a preferred azimuthal orientation, which poses challenges for orientation estimation and refinement. We developed a strategy for recording and processing electron cryomicroscopic images that differs fi om classical two-dimensional crystalline reconstruction techniques. These developments allowed us to merge data hom tomographic tilt series of ice-embedded acrosomal bundles. The goal is to determine accurately amplitudes and phases at the diffraction maxima in terms of hkl indices, and compute a three-dimensional map from the diffraction data. (C) 1997 Academic Press.
引用
收藏
页码:245 / 256
页数:12
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