| Literature DB >> 27791004 |
Zheng Liu1, Cristina Gutierrez-Vargas2, Jia Wei2, Robert A Grassucci3, Madhumitha Ramesh4, Noel Espina5, Ming Sun2, Beril Tutuncuoglu4, Susan Madison-Antenucci5, John L Woolford4, Liang Tong2, Joachim Frank6.
Abstract
Ribosomes of trypanosomatids, a family of protozoan parasites causing debilitating human diseases, possess multiply fragmented rRNAs that together are analogous to 28S rRNA, unusually large rRNA expansion segments, and r-protein variations compared with other eukaryotic ribosomes. To investigate the architecture of the trypanosomatid ribosomes, we determined the 2.5-Å structure of the Trypanosoma cruzi ribosome large subunit by single-particle cryo-EM. Examination of this structure and comparative analysis of the yeast ribosomal assembly pathway allowed us to develop a stepwise assembly model for the eight pieces of the large subunit rRNAs and a number of ancillary "glue" proteins. This model can be applied to the characterization of Trypanosoma brucei and Leishmania spp. ribosomes as well. Together with other details, our atomic-level structure may provide a foundation for structure-based design of antitrypanosome drugs.Entities:
Keywords: Trypanosoma cruzi; antitrypanosome drug design; biogenesis; multiply fragmented rRNA; ribosome structure
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Year: 2016 PMID: 27791004 PMCID: PMC5087005 DOI: 10.1073/pnas.1614594113
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205