Specific, efficient, and selective inhibition of prokaryotic translation initiation by a novel peptide antibiotic

被引:52
作者
Brandi, L
Fabbretti, A
La Teana, A
Abbondi, M
Losi, D
Donadio, S
Gualerzi, CO [1 ]
机构
[1] Univ Camerino, Dept Biol MCA, Genet Lab, I-62032 Camerino, MC, Italy
[2] Vicuron Pharmaceut, I-21040 Gerenzano, VA, Italy
[3] Polytech Univ Marche, Inst Biochem, I-60100 Ancona, Italy
关键词
30S initiation complex; fMet-tRNA binding; P-site inhibition;
D O I
10.1073/pnas.0507740102
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many known antibiotics target the translational apparatus, but none of them can selectively inhibit initiation of protein synthesis and/or is prokaryotic-specific. This article describes the properties of GE81112, an effective and prokaryotic-specific initiation inhibitor. GE81112 is a natural tetrapeptide produced by a Streptomyces sp. identified by an in vitro high-throughput screening test developed to find inhibitors of the prokaryotic translational apparatus preferentially acting on steps other than elongation. In vivo GE81112 inhibits protein synthesis but not other cell functions such as DNA duplication, transcription, and cell wall synthesis. In vitro GE81112 was found to target the 30S ribosomal subunit and to interfere with both coded and noncoded P-site binding of fMet-tRNA, thereby selectively inhibiting formation of the 30S initiation complex.
引用
收藏
页码:39 / 44
页数:6
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