期刊
SCIENCE
卷 379, 期 6637, 页码 1123-1130出版社
AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.ade2574
关键词
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Recent advances in machine learning have allowed for the prediction of protein structure from multiple sequence alignments. By using a large language model, we are able to directly infer full atomic-level protein structure from primary sequence. This has led to a significant acceleration in high-resolution structure prediction, enabling the characterization of a large number of metagenomic proteins. Utilizing this capability, we have constructed the ESM Metagenomic Atlas, which provides insights into the diversity of natural proteins.
Recent advances in machine learning have leveraged evolutionary information in multiple sequence alignments to predict protein structure. We demonstrate direct inference of full atomic-level protein structure from primary sequence using a large language model. As language models of protein sequences are scaled up to 15 billion parameters, an atomic-resolution picture of protein structure emerges in the learned representations. This results in an order-of-magnitude acceleration of high-resolution structure prediction, which enables large-scale structural characterization of metagenomic proteins. We apply this capability to construct the ESM Metagenomic Atlas by predicting structures for >617 million metagenomic protein sequences, including >225 million that are predicted with high confidence, which gives a view into the vast breadth and diversity of natural proteins.
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