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Single particle reconstructions of the transferrin-transferrin receptor complex obtained with different specimen preparation techniques
被引:50
作者:
Cheng, YF
Wolf, E
Larvie, M
Zak, O
Aisen, P
Grigorieff, N
Harrison, SC
Walz, T
机构:
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[3] Childrens Hosp, Howard Hughes Med Inst, Boston, MA 02115 USA
[4] Yeshiva Univ Albert Einstein Coll Med, Dept Physiol & Biophys, Bronx, NY 10461 USA
[5] Brandeis Univ, Dept Biochem, Rosentstiel Basic Med Sci Res Ctr, Howard Hughes Med Inst, Waltham, MA 02454 USA
关键词:
transferrin receptor-transferrin complex;
specimen preparation;
angular reconstitution;
random conical tilt;
cryo-negative staining;
D O I:
10.1016/j.jmb.2005.11.021
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:
The outcome of three-dimensional (3D) reconstructions in single particle electron microscopy (EM) depends on a number of parameters. We have used the well-characterized structure of the transferrin (Tf)-transferrin receptor (TfR) complex to study how specimen preparation techniques influence the outcome of single particle EM reconstructions. The Tf-TfR complex is small (290 kDa) and of low symmetry (2-fold). Angular reconstitution from images of vitrified specimens does not reliably converge on the correct structure. Random conical tilt reconstructions from negatively stained specimens are reliable, but show variable degrees of artifacts depending on the negative staining protocol. Alignment of class averages from vitrified specimens to a 3D negative stain reference model using FREALIGN largely eliminated artifacts in the resulting 3D maps, but not completely. Our results stress the need for critical evaluation of structures determined by single particle EM. (c) 2005 Elsevier Ltd. All rights reserved.
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页码:1048 / 1065
页数:18
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