Segmental isotopic labeling by asparaginyl endopeptidase-mediated protein ligation

被引:18
|
作者
Mikula, Kornelia M. [1 ]
Krumwiede, Luisa [1 ]
Plueckthun, Andreas [2 ]
Iwai, Hideo [1 ]
机构
[1] Univ Helsinki, Res Program Struct Biol & Biophys, Inst Biotechnol, POB 65, FIN-00014 Helsinki, Finland
[2] Univ Zurich, Dept Biochem, Winterthurerstr 190, CH-8057 Zurich, Switzerland
基金
芬兰科学院;
关键词
Asparaginyl endopeptidase; Designed armadillo repeat protein; Segmental isotopic labeling; Protein trans-ligation; Protein NMR; ARMADILLO REPEAT PROTEINS; NATIVE CHEMICAL LIGATION; MULTIDOMAIN PROTEINS; STRUCTURAL BASIS; PEPTIDE-BINDING; LARGER PROTEIN; DNAE INTEIN; IN-VIVO; SORTASE; DOMAIN;
D O I
10.1007/s10858-018-0175-4
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
Segmental isotopic labeling can facilitate NMR studies of large proteins, multi-domain proteins, and proteins with repetitive sequences by alleviating NMR signal overlaps. Segmental isotopic labeling also allows us to investigate an individual domain in the context of a full-length protein by NMR. Several established methods are available for segmental isotopic labeling such as intein-mediated ligation, but each has specific requirements and limitations. Here, we report an enzymatic approach using bacterially produced asparagine endopeptidase from Oldenlandia affinis for segmental isotopic labeling of a protein with repetitive sequences, a designed armadillo repeat protein, by overcoming some of the shortcomings of enzymatic ligation for segmental isotopic labeling.
引用
收藏
页码:225 / 235
页数:11
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