(H)N(COCA)NH and (HN)under-bar(COCA)NH experiments for H-1-N-15 backbone assignments in C-13/N-15-labeled proteins

被引:42
作者
Bracken, C
Palmer, AG
Cavanagh, J
机构
[1] NEW YORK STATE DEPT HLTH,WADSWORTH CTR LABS & RES,NMR,STRUCT BIOL FACIL,ALBANY,NY 12201
[2] COLUMBIA UNIV,DEPT BIOCHEM & MOL BIOPHYS,NEW YORK,NY 10032
关键词
triple resonance NMR spectroscopy; sequential assignment; proteins;
D O I
10.1023/A:1018679819693
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
Triple resonance HN(COCA)NH pulse sequences for correlating H-1((i)), H-15((i)), H-1((i-1)), and N-15((i-1)) spins that utilize overlapping coherence transfer periods provide increased sensitivity relative to pulse sequences that utilize sequential coherence transfer periods. Although the overlapping sequence elements reduce the overall duration of the pulse sequences, the principal benefit derives from a reduction in the number of 180 degrees pulses. Two versions of the technique are presented: a 3D (H)N(COCA)NH experiment that correlates N-15((i)), H-1((i-1)), and N-15((i-1)) spins, and a 3D <(HN)under bar (COCA)NH> experiment that correlates H-1((i)), N-15((i)), H-1((i-1)), and N-15((i-1)) spins by simultaneously encoding the H-1((i)) and N-15((i)) chemical shifts during the t(1) evolution period. The methods are demonstrated on a C-13/N-15-enriched sample of the protein ubiquitin and are easily adapted for application to H-2/C-13/N-15-enriched proteins.
引用
收藏
页码:94 / 100
页数:7
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