A robust and cost-effective method for the production of Val, Leu, Ile (δ1) methyl-protonated 15N-, 13C-, 2H-labeled proteins

被引:426
作者
Goto, NK [1 ]
Gardner, KH
Mueller, GA
Willis, RC
Kay, LE
机构
[1] Univ Toronto, Dept Biochem, Toronto, ON M5S 1A8, Canada
[2] Hosp Sick Children, Dept Biochem & Struct Biol, Toronto, ON M5S 1X8, Canada
[3] Univ Toronto, Prot Engn Network Ctr Excellence, Toronto, ON M5S 1A8, Canada
[4] Univ Toronto, Dept Med Genet & Microbiol, Toronto, ON M5S 1A8, Canada
[5] Univ Toronto, Dept Biochem, Toronto, ON M5S 1A8, Canada
[6] Univ Toronto, Dept Chem, Toronto, ON M5S 1A8, Canada
基金
英国医学研究理事会; 加拿大自然科学与工程研究理事会;
关键词
deuteration; alpha-ketobutyrate; alpha-ketoisovalerate; methyl protonation;
D O I
10.1023/A:1008393201236
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
A selective protonation strategy is described that uses [3-H-2] C-13 alpha-ketoisovalerate to introduce (H-1-delta methyl)leucine and (H-1-gamma methyl)-valine into N-15-, C-13-, H-2-labeled proteins. A minimum level of 90% incorporation of label into both leucine and valine methyl groups is obtained by inclusion of approximate to 100 mg/L alpha-ketoisovalerate in the bacterial growth medium. Addition of [3,3-H-2(2)] alpha-ketobutyrate to the expression media (D2O solvent) results in the production of proteins with (H-1-delta 1 methyl)-isoleucine (>90% incorporation). H-1-C-13 HSQC correlation spectroscopy establishes that CH2D and CHD2 isotopomers are not produced with this method. This approach offers enhanced labeling of Leu methyl groups over previous methods that utilize Val as the labeling agent and is more cost effective.
引用
收藏
页码:369 / 374
页数:6
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