NMR techniques for very large proteins and RNAs in solution

被引:73
|
作者
Tzakos, Andreas G.
Grace, Christy R. R.
Lukavsky, Peter J.
Riek, Roland
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
[2] Salk Inst Biol Studies, Struct Biol Lab, La Jolla, CA 92037 USA
来源
ANNUAL REVIEW OF BIOPHYSICS AND BIOMOLECULAR STRUCTURE | 2006年 / 35卷
基金
英国医学研究理事会;
关键词
TROSY; CRIPT; cross-correlated relaxation; RDCs;
D O I
10.1146/annurev.biophys.35.040405.102034
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
Three-dimensional structure determination of small proteins and oligonucleotides by solution NMR is established. With the development of novel NMR and labeling techniques, structure determination is now feasible for proteins with a molecular mass of up to similar to 100 kDa and RNAs of up to 35 kDa. Beyond these molecular. required for applying masses special techniques and approaches are NMR as a multiprobe method for structural investigations of proteins and RNAs. It is the aim of this review to summarize the NMR techniques and approaches available to advance the molecular mass limit of NMR both for proteins (up to I MDa) and RNAs (up to 100 kDa). Physical pictures of the novel techniques, their experimental applications, as well as labeling and assignment strategies are discussed and accompanied by future perspectives.
引用
收藏
页码:319 / 342
页数:24
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