Ribosome-mediated synthesis of natural product-like peptides via cell-free translation

被引:31
|
作者
Maini, Rumit [1 ]
Umemoto, Shiori [1 ]
Suga, Hiroaki [1 ,2 ]
机构
[1] Univ Tokyo, Dept Chem, Grad Sch Sci, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1130033, Japan
[2] JST, CREST, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1130033, Japan
关键词
IN-VITRO SELECTION; BETA-AMINO ACIDS; MACROCYCLIC PEPTIDES; STRUCTURAL BASIS; CYCLIC-PEPTIDES; DRUG DISCOVERY; INHIBITORS; LIBRARIES; BIOSYNTHESIS; PERMEABILITY;
D O I
10.1016/j.cbpa.2016.06.006
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
Peptide natural products (PNPs) represent a unique class of compounds known for their fascinating structural motifs with important biological activities. Lately, PNPs have garnered a lot of interest for their application in drug discovery. Nevertheless, lack of diversity oriented synthetic/biosynthetic platforms to generate large natural product-like libraries has limited their development as peptide therapeutics. The promiscuity of cell free translation has allowed for the synthesis of artificial PNPs having complex structural features. Modified cell-free translation systems coupled with the display technologies have generated diverse natural product-like peptide libraries and led to the discovery of several biologically active molecules. Such technologies have drastically decreased the time to obtain peptide drug leads and therefore, revolutionized the field of peptide drug discovery. In this account, we review recent developments in the synthesis of natural product-like peptides via cell-free translation.
引用
收藏
页码:44 / 52
页数:9
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