Literature DB >> 25278503

Structure of the large ribosomal subunit from human mitochondria.

Alan Brown1, Alexey Amunts1, Xiao-Chen Bai1, Yoichiro Sugimoto1, Patricia C Edwards1, Garib Murshudov1, Sjors H W Scheres1, V Ramakrishnan1.   

Abstract

Human mitochondrial ribosomes are highly divergent from all other known ribosomes and are specialized to exclusively translate membrane proteins. They are linked with hereditary mitochondrial diseases and are often the unintended targets of various clinically useful antibiotics. Using single-particle cryogenic electron microscopy, we have determined the structure of its large subunit to 3.4 angstrom resolution, revealing 48 proteins, 21 of which are specific to mitochondria. The structure unveils an adaptation of the exit tunnel for hydrophobic nascent peptides, extensive remodeling of the central protuberance, including recruitment of mitochondrial valine transfer RNA (tRNA(Val)) to play an integral structural role, and changes in the tRNA binding sites related to the unusual characteristics of mitochondrial tRNAs.
Copyright © 2014, American Association for the Advancement of Science.

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Year:  2014        PMID: 25278503      PMCID: PMC4246062          DOI: 10.1126/science.1258026

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  116 in total

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