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| Main Authors: | , , |
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| Format: | Preprint |
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2025
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| Subjects: | |
| Online Access: | https://arxiv.org/abs/2501.06371 |
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| _version_ | 1866912184211079168 |
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| author | Pandey, Akash Chen, Wei Keten, Sinan |
| author_facet | Pandey, Akash Chen, Wei Keten, Sinan |
| contents | The properties of biological materials like proteins and nucleic acids are largely determined by their primary sequence. While certain segments in the sequence strongly influence specific functions, identifying these segments, or so-called motifs, is challenging due to the complexity of sequential data. While deep learning (DL) models can accurately capture sequence-property relationships, the degree of nonlinearity in these models limits the assessment of monomer contributions to a property - a critical step in identifying key motifs. Recent advances in explainable AI (XAI) offer attention and gradient-based methods for estimating monomeric contributions. However, these methods are primarily applied to classification tasks, such as binding site identification, where they achieve limited accuracy (40-45%) and rely on qualitative evaluations. To address these limitations, we introduce a DL model with interpretable steps, enabling direct tracing of monomeric contributions. We also propose a metric ($\mathcal{I}$), inspired by the masking technique in the field of image analysis and natural language processing, for quantitative analysis on datasets mainly containing distinct properties of anti-cancer peptides (ACP), antimicrobial peptides (AMP), and collagen. Our model exhibits 22% higher explainability, pinpoints critical motifs (RRR, RRI, and RSS) that significantly destabilize ACPs, and identifies motifs in AMPs that are 50% more effective in converting non-AMPs to AMPs. These findings highlight the potential of our model in guiding mutation strategies for designing protein-based biomaterials. |
| format | Preprint |
| id |
arxiv_https___arxiv_org_abs_2501_06371 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | COLOR: A compositional linear operation-based representation of protein sequences for identification of monomer contributions to properties Pandey, Akash Chen, Wei Keten, Sinan Biomolecules The properties of biological materials like proteins and nucleic acids are largely determined by their primary sequence. While certain segments in the sequence strongly influence specific functions, identifying these segments, or so-called motifs, is challenging due to the complexity of sequential data. While deep learning (DL) models can accurately capture sequence-property relationships, the degree of nonlinearity in these models limits the assessment of monomer contributions to a property - a critical step in identifying key motifs. Recent advances in explainable AI (XAI) offer attention and gradient-based methods for estimating monomeric contributions. However, these methods are primarily applied to classification tasks, such as binding site identification, where they achieve limited accuracy (40-45%) and rely on qualitative evaluations. To address these limitations, we introduce a DL model with interpretable steps, enabling direct tracing of monomeric contributions. We also propose a metric ($\mathcal{I}$), inspired by the masking technique in the field of image analysis and natural language processing, for quantitative analysis on datasets mainly containing distinct properties of anti-cancer peptides (ACP), antimicrobial peptides (AMP), and collagen. Our model exhibits 22% higher explainability, pinpoints critical motifs (RRR, RRI, and RSS) that significantly destabilize ACPs, and identifies motifs in AMPs that are 50% more effective in converting non-AMPs to AMPs. These findings highlight the potential of our model in guiding mutation strategies for designing protein-based biomaterials. |
| title | COLOR: A compositional linear operation-based representation of protein sequences for identification of monomer contributions to properties |
| topic | Biomolecules |
| url | https://arxiv.org/abs/2501.06371 |