Four guidelines to identify bona fide protease–substrate pairs

Plant proteases are an important class of enzymes, with proposed involvement in various aspects of the plant life cycle. However, pinpointing authentic protease-substrate interactions remains challenging, which hinders a comprehensive understanding of the biological function of proteases. Moreover, a structured set of guidelines to validate protease substrates is lacking. In this review, we outline a minimum of four key guidelines that, when followed, can confirm the specificity of protease-substrate interaction for proteases that perform limited proteolysis and with specific cleavage sites: (i) the observation of substrate cleavage; (ii) the reduction in substrate cleavage due to protease inhibitors or (iii) genetic mutation of the protease; and (iv) a final proof of the specificity of the substrate cleavage site. It is important to emphasize that these guidelines are not universally applicable to all proteases. By creating a set of guidelines, summarizing current findings and proposing future research directions, this review aims to highlight innovative techniques that will improve the specificity and accuracy of protease research and facilitate a deeper understanding of the role of proteases in plant biology.

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Publication Details

Journal
Journal of Experimental Botany
Published
2025-05-08
DOI
https://doi.org/10.1093/jxb/eraf194
Citations
2
Primary Topic
Insect Resistance and Genetics
Type
article
Field-Weighted Citation Impact
1.61

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article

Four guidelines to identify bona fide protease–substrate pairs

Yong Zou, Simon Stael, Qun Yang, Shamik Mazumdar et al.
2 citations
Journal of Experimental Botany
Insect Resistance and Genetics
1.61
article

Four guidelines to identify bona fide protease–substrate pairs

Yong Zou, Simon Stael, Qun Yang, Shamik Mazumdar, Maxence James, Shuolin Qi
article en
2 citations

Abstract

Plant proteases are an important class of enzymes, with proposed involvement in various aspects of the plant life cycle. However, pinpointing authentic protease-substrate interactions remains challenging, which hinders a comprehensive understanding of the biological function of proteases. Moreover, a structured set of guidelines to validate protease substrates is lacking. In this review, we outline a minimum of four key guidelines that, when followed, can confirm the specificity of protease-substrate interaction for proteases that perform limited proteolysis and with specific cleavage sites: (i) the observation of substrate cleavage; (ii) the reduction in substrate cleavage due to protease inhibitors or (iii) genetic mutation of the protease; and (iv) a final proof of the specificity of the substrate cleavage site. It is important to emphasize that these guidelines are not universally applicable to all proteases. By creating a set of guidelines, summarizing current findings and proposing future research directions, this review aims to highlight innovative techniques that will improve the specificity and accuracy of protease research and facilitate a deeper understanding of the role of proteases in plant biology.

Journal of Experimental BotanyVol. 76(15)
Swedish University of Agricultural Sciences (SE)
Knut och Alice Wallenbergs Stiftelse
Responsible consumption and production
Openalex Percentile: Top 17%
Insect Resistance and Genetics
1.61
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