Recent advances in sortase-catalyzed ligation methodology

被引:120
作者
Antos, John M. [1 ]
Truttmann, Matthias C. [2 ]
Ploegh, Hidde L. [2 ]
机构
[1] Western Washington Univ, Dept Chem, 516 High St, Bellingham, WA 98229 USA
[2] Whitehead Inst Biomed Res, Cambridge Ctr 9, Cambridge, MA 02142 USA
基金
瑞士国家科学基金会;
关键词
STAPHYLOCOCCUS-AUREUS SORTASE; SITE-SPECIFIC MODIFICATION; PROTEIN LIGATION; IMMOBILIZED SORTASE; MEDIATED LIGATIONS; BUTELASE; PURIFICATION; SPECIFICITY; STEP; CYCLIZATION;
D O I
10.1016/j.sbi.2016.05.021
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
The transpeptidation reaction catalyzed by bacterial sortases continues to see increasing use in the construction of novel protein derivatives. In addition to growth in the number of applications that rely on sortase, this field has also seen methodology improvements that enhance reaction performance and scope. In this opinion, we present an overview of key developments in the practice and implementation of sortase-based strategies, including applications relevant to structural biology. Topics include the use of engineered sortases to increase reaction rates, the use of redesigned acyl donors and acceptors to mitigate reaction reversibility, and strategies for expanding the range of substrates that are compatible with a sortase-based approach.
引用
收藏
页码:111 / 118
页数:8
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