Evaluation of stereo-array isotope labeling (SAIL) patterns for automated structural analysis of proteins with CYANA

被引:32
作者
Ikeya, Teppei
Terauchi, Tsutomu
Guentert, Peter
Kainosho, Masatsune
机构
[1] Tokyo Metropolitan Univ, Grad Sch Sci, Hachioji, Tokyo 1920397, Japan
[2] Japan Biol Informat Consortium, Tokyo, Japan
[3] JST, CREST, Hachioji, Tokyo 1920397, Japan
[4] RIKEN, Genom Sci Ctr, Tatsuo Miyazawa Mem Program, Yokohama, Kanagawa 2300045, Japan
关键词
NMR; H-1; N-15; C-13; SAIL; protein structure; CYANA;
D O I
10.1002/mrc.1815
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently we have developed the stereo-array isotope labeling (SAIL) technique to overcome the conventional molecular size limitation in NMR protein structure determination by employing complete stereo- and regiospecific patterns of stable isotopes. SAIL sharpens signals and simplifies spectra without the loss of requisite structural information, thus making large classes of proteins newly accessible to detailed solution structure determination. The automated structure calculation program CYANA can efficiently analyze SAIL-NOESY spectra and calculate structures without manual analysis. Nevertheless, the original SAIL method might not be capable of determining the structures of proteins larger than 50 kDa or membrane proteins, for which the spectra are characterized by many broadened and overlapped peaks. Here we have carried out simulations of new SAIL patterns optimized for minimal relaxation and overlap, to evaluate the combined use of SAIL and CYANA for solving the structures of larger proteins and membrane proteins. The modified approach reduces the number of peaks to nearly half of that observed with uniform labeling, while still yielding well-defined structures and is expected to enable NMR structure determinations of these challenging systems. Copyright (C) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:S152 / S157
页数:6
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