Selective N-terminal fluorescent labeling of proteins using 4-chloro-7-nitrobenzofurazan: A method to distinguish protein N-terminal acetylation

被引:26
|
作者
Bernal-Perez, Lina F. [1 ]
Prokai, Laszlo [2 ]
Ryu, Youngha [1 ]
机构
[1] Texas Christian Univ, Dept Chem, Ft Worth, TX 76129 USA
[2] Univ N Texas, Hlth Sci Ctr, Dept Mol Biol & Immunol, Ft Worth, TX 76107 USA
关键词
Protein N-terminal acetylation; Fluorescent labeling; NBD-Cl; Z-domain; Thymosin; RIBOSOMAL-PROTEINS; THYMOSIN ALPHA-1; Z-DOMAIN; RIMJ; METHYLTRANSFERASE; IDENTIFICATION; CLONING;
D O I
10.1016/j.ab.2012.05.026
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A fluorogenic derivatization method was developed to distinguish the protein N-terminal acetylation status. The unacetylated protein selectively reacted with 4-chloro-7-nitrobenzofurazan (NBD-Cl) at neutral pH to provide high fluorescence. In contrast, the protein with N-terminal acetylation was essentially nonfluorescent under the same conditions despite the presence of many internal lysine residues. Fluorescence of the NBD-labeled protein was very stable, and only micromolar concentrations of proteins were required for reliable detection. This method also provides a general and practical way to quantify proteins when their N-terminal amino group is available. (c) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:13 / 15
页数:3
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