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用于同时确定大蛋白质中 Alaβ 和 Ileγ2 甲基基团的甲基检测“往返”核磁共振实验。

Methyl-detected 'out-and-back' NMR experiments for simultaneous assignments of Alabeta and Ilegamma2 methyl groups in large proteins.

作者信息

Sheppard Devon, Guo Chenyun, Tugarinov Vitali

机构信息

Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, USA.

出版信息

J Biomol NMR. 2009 Apr;43(4):229-38. doi: 10.1007/s10858-009-9305-3. Epub 2009 Mar 10.

Abstract

A set of sensitive methyl-detected 'out-and-back' NMR experiments for simultaneous assignments of Alabeta and Ilegamma2 methyl positions in large proteins is described. The developed methodology is applied to an 82-kDa enzyme Malate Synthase G. Complete alanine beta and isoleucine gamma2 1H-13C methyl chemical shift assignments could be obtained from the set of new methyl-detected 'out-and-back' 3D experiments. The described methodology for methyl assignments should be applicable to protein molecules within approximately 100-kDa molecular weight range irrespective of the labeling strategy chosen to produce selectively protonated Alabeta and Ilegamma2 13CH3 sites on a deuterated background.

摘要

本文描述了一组灵敏的甲基检测“往返”核磁共振实验,用于同时确定大蛋白质中 Alaβ 和 Ileγ2 甲基位置。所开发的方法应用于 82 kDa 的苹果酸合酶 G。从这组新的甲基检测“往返”三维实验中可以获得完整的丙氨酸β和异亮氨酸γ2 的 1H-13C 甲基化学位移归属。所描述的甲基归属方法应适用于分子量约为 100 kDa 范围内的蛋白质分子,而与为在氘代背景上产生选择性质子化的 Alaβ 和 Ileγ2 13CH3 位点所选择的标记策略无关。

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