Site-specific incorporation of a fluorescent terphenyl unnatural amino acid

被引:18
|
作者
Lampkowski, Jessica S. [1 ]
Uthappa, Diya M. [1 ]
Young, Douglas D. [1 ]
机构
[1] Coll William & Mary, Dept Chem, Williamsburg, VA 23187 USA
关键词
Unnatural amino acids; Green fluorescent protein; Fluorescent sensors; Protein expression; Aminoacyl-tRNA synthetase; EXPANDED GENETIC-CODE; ESCHERICHIA-COLI; LIVING CELLS; CHEMICAL AMINOACYLATION; FUSION PROTEINS; TRANSFER-RNA; P-TERPHENYL; PROBES; DYNAMICS; CONJUGATION;
D O I
10.1016/j.bmcl.2015.09.050
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The site-specific incorporation of unnatural amino acids into proteins has a wide range of biological implications. Of particular interest is the incorporation of fluorescent probes as a mechanism to track protein function, transport, and folding. Thus, the development of a novel system for the incorporation of new fluorescent unnatural amino acids has significant utility. Specifically, we have elucidated an aminoacyl-tRNA synthetase capable of recognizing a terphenyl UAA derivative, and charging a cognate tRNA with this amino acid for protein incorporation. Moreover, we have successfully incorporated this fluorescent UAA into GFP at several key residues, demonstrating a novel means to modulate fluorescence within the protein. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5277 / 5280
页数:4
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