| Literature DB >> 29107485 |
Jailson Brito Querido1, Eder Mancera-Martínez1, Quentin Vicens1, Anthony Bochler1, Johana Chicher2, Angelita Simonetti1, Yaser Hashem3.
Abstract
Kinetoplastids are potentially lethal protozoan pathogens affecting more than 20 million people worldwide. There is a critical need for more specific targets for the development of safer anti-kinetoplastid therapeutic molecules that can replace the scarce and highly cytotoxic current drugs. The kinetoplastid ribosome represents a potential therapeutic target due to its relative structural divergence when compared with its human counterpart. However, several kinetoplastid-specific ribosomal features remain uncharacterized. Here, we present the near-atomic cryoelectron microscopy structure of a novel bona fide kinetoplastid-specific ribosomal (r-) protein (KSRP) bound to the ribosome. KSRP is an essential protein located at the solvent face of the 40S subunit, where it binds and stabilizes kinetoplastid-specific domains of rRNA, suggesting its role in ribosome integrity. KSRP also interacts with the r-protein eS6 at a region that is only conserved in kinetoplastids. The kinetoplastid-specific ribosomal environment of KSRP provides a promising target for the design of safer anti-kinetoplastidian drugs.Entities:
Keywords: cryo-EM; kinetoplastid-specific ribosomal protein; kinetoplastids; ribosome
Mesh:
Substances:
Year: 2017 PMID: 29107485 DOI: 10.1016/j.str.2017.09.014
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006