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tRNA selection and kinetic proofreading in translation

โœ Scribed by Blanchard, Scott C; Gonzalez, Ruben L; Kim, Harold D; Chu, Steven; Puglisi, Joseph D


Book ID
109966888
Publisher
Nature Publishing Group
Year
2004
Tongue
English
Weight
780 KB
Volume
11
Category
Article
ISSN
1545-9993

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โœฆ Synopsis


Using single-molecule methods we observed the stepwise movement of aminoacyl-tRNA (aa-tRNA) into the ribosome during selection and kinetic proofreading using single-molecule fluorescence resonance energy transfer (smFRET). Intermediate states in the pathway of tRNA delivery were observed using antibiotics and nonhydrolyzable GTP analogs. We identified three unambiguous FRET states corresponding to initial codon recognition, GTPase-activated and fully accommodated states. The antibiotic tetracycline blocks progression of aa-tRNA from the initial codon recognition state, whereas cleavage of the sarcinricin loop impedes progression from the GTPase-activated state. Our data support a model in which ribosomal recognition of correct codon-anticodon pairs drives rotational movement of the incoming complex of EF-Tu-GTP-aa-tRNA toward peptidyl-tRNA during selection on the ribosome. We propose a mechanistic model of initial selection and proofreading.


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Two simpli"ed kinetic proofreading scanning (KPS) models were proposed to describe the 5 cap and 3 poly(A) tail dependency of eukaryotic translation initiation. In Model I, the initiation factor complex starts scanning and unwinding the secondary structure of the 5 untranslated region (UTR) from the