Pull-Down of Metalloproteins in Their Native States by Using Desthiobiotin-Based Probes

被引:4
|
作者
Ngo, Chinh [1 ]
Mehta, Radhika [1 ]
Aggarwal, Kanchan [1 ]
Fikes, Audrey G. [1 ]
Santos, Ines C. [1 ]
Greer, Sylvester M. [1 ]
Que, Emily L. [1 ]
机构
[1] Univ Texas Austin, Dept Chem, 105 E 24th St,Stop A5300, Austin, TX 78712 USA
关键词
carbonic anhydrase; desthiobiotin; metalloproteins; proteomics; sulfonamide; ZINC-REQUIRING ECTOENZYMES; CARBONIC-ANHYDRASE; BINDING; PROTEINS; COPPER; METALLOCHAPERONES; ACTIVATION; CHALLENGES; INHIBITORS; PLASMA;
D O I
10.1002/cbic.201800613
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
One-third of all proteins are estimated to require metals for structural stability and/or catalytic activity. Desthiobiotin probes containing metal binding groups can be used to capture metalloproteins with exposed active-site metals under mild conditions so as to prevent changes in metallation state. The proof-of-concept was demonstrated with carbonic anhydrase (CA), an open active site, Zn2+-containing protein. CA was targeted by using sulfonamide derivatives. Linkers of various lengths and structures were screened to determine the optimal structure for capture of the native protein. The optimized probes could selectively pull down CA from red blood cell lysate and other protein mixtures. Pull-down of differently metallated CAs was also investigated.
引用
收藏
页码:1003 / 1007
页数:5
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