Konrat R, Muhandiram D R, Farrow N A, Kay L E
Protein Engineering Network of Centres of Excellence, University of Toronto, ON, Canada.
J Biomol NMR. 1997 Jun;9(4):409-22. doi: 10.1023/a:1018354712430.
Pulse sequences are presented for the measurement of 3JC'C gamma and 3JNC gamma scalar couplings for all C gamma containing residues in 15N,13C uniformly labeled proteins. The methods described are based on quantitative J correlation spectroscopy pioneered by Bax and co-workers [Bax et. al. (1994) Methods Enzymol., 239, 79-105]. The combination of 3JC'C gamma and 3JNC gamma scalar coupling constants allows the assignment of discrete rotameric states about the chi 1 torsion angle in cases where such states exist or, alternatively, facilitates the establishment of noncanonical chi 1 conformations or the presence of rotameric averaging. The methods are applied to a 1.5 mM sample of staphylococcal nuclease.
给出了用于测量15N、13C均匀标记蛋白质中所有含Cγ残基的3JC'Cγ和3JNCγ标量耦合的脉冲序列。所描述的方法基于Bax及其同事开创的定量J相关光谱法[Bax等人(1994年)《酶学方法》,239,79 - 105]。在存在离散旋转异构体状态的情况下,3JC'Cγ和3JNCγ标量耦合常数的组合允许确定围绕χ1扭转角的离散旋转异构体状态,或者有助于建立非规范的χ1构象或旋转异构体平均化的存在。这些方法应用于1.5 mM的葡萄球菌核酸酶样品。