Deep learning guided design of protease substrates

Proteases, enzymes that play critical roles in health and disease, exert their function through the cleavage of peptide bonds. Identifying substrates that are efficiently and selectively cleaved by target proteases is essential for studying protease activity and for harnessing it in protease-activated diagnostics and therapeutics. However, the vast design space of possible substrates (c.a. 20<sup>10</sup> amino acid combinations for a 10-mer peptide) and the limited accessibility of high-throughput activity profiling tools hinder the speed and success of substrate design. We present CleaveNet, an end-to-end AI pipeline for the design of protease substrates. Applied to matrix metalloproteinases, CleaveNet enhances the scale, tunability, and efficiency of substrate design. CleaveNet generates peptide substrates that exhibit sound biophysical properties and capture not only well-established but also previously-uncharacterized cleavage motifs. To control substrate design, CleaveNet incorporates a conditioning tag that steers peptide generation towards desired cleavage profiles, enabling targeted design of efficient and selective substrates. CleaveNet-generated substrates were validated experimentally through a large-scale in vitro screen, even in the challenging case of designing highly selective substrates for MMP13. We envision that CleaveNet will accelerate our ability to study and capitalize on protease activity, paving the way for in silico design tools across enzyme classes.

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Publication Details

Journal
Nature Communications
Published
2026-01-06
DOI
https://doi.org/10.1038/s41467-025-67226-1
Primary Topic
Biochemical and Structural Characterization
Type
article
Field-Weighted Citation Impact
0.00

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article

Deep learning guided design of protease substrates

Sangeeta N. Bhatia, Sarah Barzegari Alamdari, Tahoura Samad, Carmen Martín-Alonso et al.
Nature Communications
Biochemical and Structural Characterization
article

Deep learning guided design of protease substrates

Sangeeta N. Bhatia, Sarah Barzegari Alamdari, Tahoura Samad, Carmen Martín-Alonso, Ava Amini, Kevin K. Yang
article en

Abstract

Proteases, enzymes that play critical roles in health and disease, exert their function through the cleavage of peptide bonds. Identifying substrates that are efficiently and selectively cleaved by target proteases is essential for studying protease activity and for harnessing it in protease-activated diagnostics and therapeutics. However, the vast design space of possible substrates (c.a. 20<sup>10</sup> amino acid combinations for a 10-mer peptide) and the limited accessibility of high-throughput activity profiling tools hinder the speed and success of substrate design. We present CleaveNet, an end-to-end AI pipeline for the design of protease substrates. Applied to matrix metalloproteinases, CleaveNet enhances the scale, tunability, and efficiency of substrate design. CleaveNet generates peptide substrates that exhibit sound biophysical properties and capture not only well-established but also previously-uncharacterized cleavage motifs. To control substrate design, CleaveNet incorporates a conditioning tag that steers peptide generation towards desired cleavage profiles, enabling targeted design of efficient and selective substrates. CleaveNet-generated substrates were validated experimentally through a large-scale in vitro screen, even in the challenging case of designing highly selective substrates for MMP13. We envision that CleaveNet will accelerate our ability to study and capitalize on protease activity, paving the way for in silico design tools across enzyme classes.

Nature CommunicationsVol. 17(1)
Broad Institute (US), Microsoft (United States) (US), Howard Hughes Medical Institute (US), Harvard–MIT Division of Health Sciences and Technology (US), MIT-Harvard Center for Ultracold Atoms (US), Microsoft Research (United Kingdom) (GB), Massachusetts Institute of Technology (US)
“la Caixa” Foundation, Broad Institute, Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Ludwig Center at Harvard
Openalex Percentile: Top 94%
Biochemical and Structural Characterization
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