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Unusual Post-Translational Modifications in the Biosynthesis of Lasso Peptides.

Yuwei DuanWeijing NiuLinlin PangXiaoying BianYouming ZhangGuannan Zhong
Published in: International journal of molecular sciences (2022)
Lasso peptides are a subclass of ribosomally synthesized and post-translationally modified peptides (RiPPs) and feature the threaded, lariat knot-like topology. The basic post-translational modifications (PTMs) of lasso peptide contain two steps, including the leader peptide removal of the ribosome-derived linear precursor peptide by an ATP-dependent cysteine protease, and the macrolactam cyclization by an ATP-dependent macrolactam synthetase. Recently, advanced bioinformatic tools combined with genome mining have paved the way to uncover a rapidly growing number of lasso peptides as well as a series of PTMs other than the general class-defining processes. Despite abundant reviews focusing on lasso peptide discoveries, structures, properties, and physiological functionalities, few summaries concerned their unique PTMs. In this review, we summarized all the unique PTMs of lasso peptides uncovered to date, shedding light on the related investigations in the future.
Keyphrases
  • amino acid
  • machine learning
  • high resolution
  • systematic review
  • gene expression
  • genome wide
  • fluorescent probe