Mechanistic Insight into the Cleavage Site Specificity of <i>Vibrio</i> Collagenase VhaC to the Y–G Bonds in Collagen

M9 collagenases have various biotechnological and medical applications due to their high activity and specificity to collagen. Although the collagenolytic mechanism of M9 collagenases has been studied, the molecular basis for their cleavage site specificity remains unknown. Here, the mechanism of the Y-G bond cleavage site specificity of M9 collagenase VhaC was studied. The double-G motif (G441 and G442) and Y549 of VhaC define a narrow S1' substrate binding pocket responsible for P1' substrate binding, among which Y549 functions as the structural determinant for the specific recognition of P1' glycine, because its bulky side chain restricts the accommodation of residues with a side chain. The S1' tyrosine corresponding to Y549 in VhaC is strictly conserved among M9 collagenases, suggesting its significance in the cleavage site specificity. This study advances the applications of M9 collagenases in disease treatment and collagen oligopeptide production.

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Publication Details

Journal
Journal of Agricultural and Food Chemistry
Published
2025-08-22
DOI
https://doi.org/10.1021/acs.jafc.5c06270
Primary Topic
Blood properties and coagulation
Type
article
Field-Weighted Citation Impact
0.00

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article

Mechanistic Insight into the Cleavage Site Specificity of Vibrio Collagenase VhaC to the Y–G Bonds in Collagen

Xiu‐Lan Chen, Chao Gao, Peng Wang, Rui Liu et al.
Journal of Agricultural and Food Chemistry
Blood properties and coagulation
article

Mechanistic Insight into the Cleavage Site Specificity of Vibrio Collagenase VhaC to the Y–G Bonds in Collagen

Xiu‐Lan Chen, Chao Gao, Peng Wang, Rui Liu, Dandan Wang, Haiyan Cao, Yu‐Zhong Zhang, Wenxiao Zhao, Yan Wang
article en

Abstract

M9 collagenases have various biotechnological and medical applications due to their high activity and specificity to collagen. Although the collagenolytic mechanism of M9 collagenases has been studied, the molecular basis for their cleavage site specificity remains unknown. Here, the mechanism of the Y-G bond cleavage site specificity of M9 collagenase VhaC was studied. The double-G motif (G441 and G442) and Y549 of VhaC define a narrow S1' substrate binding pocket responsible for P1' substrate binding, among which Y549 functions as the structural determinant for the specific recognition of P1' glycine, because its bulky side chain restricts the accommodation of residues with a side chain. The S1' tyrosine corresponding to Y549 in VhaC is strictly conserved among M9 collagenases, suggesting its significance in the cleavage site specificity. This study advances the applications of M9 collagenases in disease treatment and collagen oligopeptide production.

Journal of Agricultural and Food ChemistryVol. 73(35)
Qingdao University of Science and Technology (CN), Shandong University (CN), Institute of Marine Biotechnology (DE), Qingdao National Laboratory for Marine Science and Technology (CN), Ecologie microbienne (FR), State Key Laboratory of Microbial Technology, Ocean University of China (CN), College of Marin (US)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Taishan Scholar Project of Shandong Province, Marine S&T Fund of Shandong Province, National Key Research and Development Program of China
Zero hunger
Openalex Percentile: Top 68%
Blood properties and coagulation
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