Abstract
An affinity analog with a 5-bromoacetamido uridine 5'-phosphate moiety bonded to the 3' end of A-U-G has been prepared with the aid of polynucleotide phosphorylase. This 3'-modified, chemically reactive A-U-G analog was used to probe the ribosomal codon binding site. The yield of the reaction depended strongly on the ribosomal source and was sensitive to salt-washing ribosomes. The major crosslinking product was identified to be protein S1. Since the reaction of this 3'-modified A-U-G programmed ribosomes for Met-tRNA-Met-M binding, it is concluded that protein S1 is located at or near the 3'-side of the ribosomal codon binding site.
MeSH Terms
Codon
Escherichia coli/metabolism
Immunodiffusion
Methionine
Molecular Weight
Oligonucleotides/metabolism
Oligoribonucleotides/metabolism
Peptide Chain Initiation, Translational
Peptide Initiation Factors
RNA, Messenger
RNA, Transfer/metabolism
Ribosomal Proteins/metabolism
Ribosomes/metabolism
Structure-Activity Relationship
Templates, Genetic
Chemicals
Codon
Oligonucleotides
Oligoribonucleotides
Peptide Initiation Factors
RNA, Messenger
Ribosomal Proteins
RNA, Transfer
Methionine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Pongs O
Stöffler G
Bald R W
References (15)
15 references, click to expand
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