Extending the Peptide/Protein Interaction Paradigm to a Protein/Protein Engagement Model in RiPP Biosynthesis

Enzymatic post-translational modification of small precursor peptides generates a wide diversity of bioactive peptidic natural products. The interaction between the precursor peptide and the peptide modifying enzyme relies on recognition of the N-terminal region of the precursor peptide─termed the leader peptide─by the modifying enzyme. In this study, we describe a model for the recognition of atypically long and highly structured nitrile hydratase-like leader peptides (NHLPs) by an azoline forming YcaO cyclodehydratase. Predicated upon the unique structure of NHLPs, the binding model relies on protein/protein interactions between higher-order secondary and tertiary structures of the NHLP and the modifying enzyme. In light of previous findings, we report that different modifying enzymes bind to different molecular surfaces of the NHLPs. These findings illustrate the modularity of different NHLP structural features and how fine-tuning of intermolecular interactions is necessary for efficient catalysis.

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Publication Details

Journal
ACS Chemical Biology
Published
2025-08-08
DOI
https://doi.org/10.1021/acschembio.5c00411
Citations
3
Primary Topic
Microbial Natural Products and Biosynthesis
Type
article
Field-Weighted Citation Impact
4.18

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article

Extending the Peptide/Protein Interaction Paradigm to a Protein/Protein Engagement Model in RiPP Biosynthesis

Andrew C. McShan, Vinayak Agarwal, Mujeeb A. Wakeel, Elizabeth A. Corbin
3 citations
ACS Chemical Biology
Microbial Natural Products and Biosynthesis
4.18
article

Extending the Peptide/Protein Interaction Paradigm to a Protein/Protein Engagement Model in RiPP Biosynthesis

Andrew C. McShan, Vinayak Agarwal, Mujeeb A. Wakeel, Elizabeth A. Corbin
article en
3 citations

Abstract

Enzymatic post-translational modification of small precursor peptides generates a wide diversity of bioactive peptidic natural products. The interaction between the precursor peptide and the peptide modifying enzyme relies on recognition of the N-terminal region of the precursor peptide─termed the leader peptide─by the modifying enzyme. In this study, we describe a model for the recognition of atypically long and highly structured nitrile hydratase-like leader peptides (NHLPs) by an azoline forming YcaO cyclodehydratase. Predicated upon the unique structure of NHLPs, the binding model relies on protein/protein interactions between higher-order secondary and tertiary structures of the NHLP and the modifying enzyme. In light of previous findings, we report that different modifying enzymes bind to different molecular surfaces of the NHLPs. These findings illustrate the modularity of different NHLP structural features and how fine-tuning of intermolecular interactions is necessary for efficient catalysis.

ACS Chemical BiologyVol. 20(9)
Georgia Institute of Technology (US)
Georgia Institute of Technology, National Institute of General Medical Sciences
Openalex Percentile: Top 6%
Microbial Natural Products and Biosynthesis
4.18
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