학술논문

Structural basis for selective stalling of human ribosome nascent chain complexes by a drug-like molecule
Document Type
Article
Source
Nature Structural and Molecular Biology; June 2019, Vol. 26 Issue: 6 p501-509, 9p
Subject
Language
ISSN
15459993; 15459985
Abstract
The drug-like molecule PF-06446846 (PF846) binds the human ribosome and selectively blocks the translation of a small number of proteins by an unknown mechanism. In structures of PF846-stalled human ribosome nascent chain complexes, PF846 binds in the ribosome exit tunnel in a eukaryotic-specific pocket formed by 28S ribosomal RNA, and alters the path of the nascent polypeptide chain. PF846 arrests the translating ribosome in the rotated state of translocation, in which the peptidyl-transfer RNA 3′-CCA end is improperly docked in the peptidyl transferase center. Selections of messenger RNAs from mRNA libraries using translation extracts reveal that PF846 can stall translation elongation, arrest termination or even enhance translation, depending on nascent chain sequence context. These results illuminate how a small molecule selectively targets translation by the human ribosome, and provides a foundation for developing small molecules that modulate the production of proteins of therapeutic interest. Structures of PF846-stalled human ribosome nascent chain complexes show that this drug-like molecule binds in the ribosome exit tunnel in a eukaryotic-specific pocket formed by 28S rRNA and alters the path of the nascent polypeptide chain.