Sheppard Devon, Guo Chenyun, Tugarinov Vitali
Department of Chemistry and Biochemistry, University of Maryland, College Park, Maryland 20742, USA.
J Biomol NMR. 2009 Apr;43(4):229-38. doi: 10.1007/s10858-009-9305-3. Epub 2009 Mar 10.
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.
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。