AI Article Synopsis

  • All proteins are created in ribosomes through a process called translation, which involves four main stages: initiation, elongation, termination, and recycling.
  • Peptide bonds are formed during the elongation phase, where transfer RNAs bring amino acids to the ribosome to build the protein one unit at a time.
  • The text breaks down the lifetime of a nascent polypeptide in the ribosome into three stages, discussing how external forces affect the polypeptide's movement and interaction with the ribosome, highlighting gaps in current research on protein synthesis.

Article Abstract

All proteins in living organisms are produced in ribosomes that facilitate the translation of genetic information into a sequence of amino acid residues. During translation, the ribosome undergoes initiation, elongation, termination, and recycling. In fact, peptide bonds are formed only during the elongation phase, which comprises periodic association of transfer RNAs and multiple auxiliary proteins with the ribosome and the addition of an amino acid to the nascent polypeptide one at a time. The protein spends a considerable amount of time attached to the ribosome. Here, we conceptually divide this portion of the protein lifetime into three stages. We define each stage on the basis of the position of the N-terminus of the nascent polypeptide within the ribosome exit tunnel and the context of the catalytic center. We argue that nascent polypeptides experience a variety of forces that determine how they translocate through the tunnel and interact with the tunnel walls. We review current knowledge about nascent polypeptide translocation and identify several white spots in our understanding of the birth of proteins.

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Source
http://dx.doi.org/10.1002/wrna.1873DOI Listing

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