蛋白激酶结构域
酵母
细胞生物学
激酶
造血
计算生物学
化学
生物
生物化学
干细胞
突变体
基因
作者
Wai Leung Lau,Bradley C. Pearce,Heather Malakian,Iyoncy Rodrigo,Dianlin Xie,Mian Gao,Frank Marsilio,ChiehYing Y. Chang,Max Ruzanov,J.K. Muckelbauer,John A. Newitt,Daša Lipovšek,S. Sheriff
标识
DOI:10.1107/s2053230x20016015
摘要
Hematopoietic progenitor kinase 1 (HPK1) is an intracellular kinase that plays an important role in modulating tumor immune response and thus is an attractive target for drug discovery. Crystallization of the wild-type HPK1 kinase domain has been hampered by poor expression in recombinant systems and poor solubility. In this study, yeast surface display was applied to a library of HPK1 kinase-domain variants in order to select variants with an improved expression level and solubility. The HPK1 variant with the most improved properties contained two mutations, crystallized readily in complex with several small-molecule inhibitors and provided valuable insight to guide structure-based drug design. This work exemplifies the benefit of yeast surface display towards engineering crystallizable proteins and thus enabling structure-based drug discovery.
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