Multimodal AI Decodes Extreme Environment Functional Dark Matter Beyond Homology
Xu, M.; Wang, D.; Liu, Q.; Jiang, H.; Liu, X.; Li, Y.; Wang, D.; Dong, H.; Yan, X.; Liu, Y.; Xu, A.; Peng, H.; Zhang, Y.; Li, H.; Li, S.; Chen, J.; Wu, X.; Wang, Y.; Li, D.; Liu, S.; Meng, L.; Li, Y.; Xue, C.; Jiang, L.; Zhang, Y.; Song, J.; Wang, M.; Guo, Y.; Li, Z.; Shen, Y.; Fu, X.; Mock, T.; Zhuang, Y.; Xue, C.; Wang, J.; Yang, H.; Xu, X.; Lee, S. M. Y.; Fan, G.; Mao, X.
Show abstract
Functional annotation of proteins from extreme environments represents a major bottleneck for bioresource discovery, as a vast reservoir of functional dark matter defies existing homology-based methods. We demonstrate that environmental pressures impart conserved physicochemical energy signatures that co-determine protein function with sequence and structure. Here we developed ACCESS, a multimodal graph neural network employing hierarchical contrastive learning with a tailored label-sample co-embedding to fuse energy, sequence, and structural information and overcome homology scarcity. ACCESS surpasses state-of-the-art methods including BLASTp and CLEAN in annotating low-identity enzymes. Applied to extreme environmental metagenomics, we constructed a function map of extremophile enzymes to expand the biocatalyst library, pinpointed functionally critical residues to guide rational design, and enabled large-scale, function-based macro-evolutionary analyses. This paradigm transcends the limitations of homology, illuminating protein dark matter and accelerating the exploration of the biospheres functional diversity for applications in biotechnology and therapeutic development.
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