Semi-Synthesis of Labeled Proteins for Spectroscopic Applications

被引:12
作者
De Rosa, Lucia [1 ]
Russomanno, Anna [1 ]
Romanelli, Alessandra [2 ]
D'Andrea, Luca Domenico [1 ]
机构
[1] CNR, Ist Biostrutture & Bioimmagini, I-80134 Naples, Italy
[2] Univ Naples Federico II, Dipartimento Sci Biol, I-80134 Naples, Italy
关键词
expressed protein ligation; intein; Forster resonance energy transfer; segmental labeling; NMR; protein labeling; RESONANCE ENERGY-TRANSFER; SMALL-MOLECULE PROBES; DNAB MINI-INTEIN; EXPRESSED PROTEIN; CHEMICAL LIGATION; MULTIDOMAIN PROTEIN; SYNTHETIC PEPTIDE; TERMINAL CYSTEINE; ESCHERICHIA-COLI; HIGHLY EFFICIENT;
D O I
10.3390/molecules18010440
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
Since the introduction of SPPS by Merrifield in the 60s, peptide chemists have considered the possibility of preparing large proteins. The introduction of native chemical ligation in the 90s and then of expressed protein ligation have opened the way to the preparation of synthetic proteins without size limitations. This review focuses on semi-synthetic strategies useful to prepare proteins decorated with spectroscopic probes, like fluorescent labels and stable isotopes, and their biophysical applications. We show that expressed protein ligation, combining the advantages of organic chemistry with the easy and size limitless recombinant protein expression, is an excellent strategy for the chemical synthesis of labeled proteins, enabling a single protein to be functionalized at one or even more distinct positions with different probes.
引用
收藏
页码:440 / 465
页数:26
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