Ab initio characterization of protein molecular dynamics with AI2BMD

Biomolecular dynamics simulation is a fundamental technology for life sciences research, and its usefulness depends on its accuracy and efficiency<sup>1-3</sup>. Classical molecular dynamics simulation is fast but lacks chemical accuracy<sup>4,5</sup>. Quantum chemistry methods such as density functional theory can reach chemical accuracy but cannot scale to support large biomolecules<sup>6</sup>. Here we introduce an artificial intelligence-based ab initio biomolecular dynamics system (AI<sup>2</sup>BMD) that can efficiently simulate full-atom large biomolecules with ab initio accuracy. AI<sup>2</sup>BMD uses a protein fragmentation scheme and a machine learning force field<sup>7</sup> to achieve generalizable ab initio accuracy for energy and force calculations for various proteins comprising more than 10,000 atoms. Compared to density functional theory, it reduces the computational time by several orders of magnitude. With several hundred nanoseconds of dynamics simulations, AI<sup>2</sup>BMD demonstrated its ability to efficiently explore the conformational space of peptides and proteins, deriving accurate <sup>3</sup>J couplings that match nuclear magnetic resonance experiments, and showing protein folding and unfolding processes. Furthermore, AI<sup>2</sup>BMD enables precise free-energy calculations for protein folding, and the estimated thermodynamic properties are well aligned with experiments. AI<sup>2</sup>BMD could potentially complement wet-lab experiments, detect the dynamic processes of bioactivities and enable biomedical research that is impossible to conduct at present.

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Publication Details

Journal
Nature
Published
2024-11-06
DOI
https://doi.org/10.1038/s41586-024-08127-z
Citations
106
Primary Topic
Protein Structure and Dynamics
Type
article
Field-Weighted Citation Impact
24.78
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article

Ab initio characterization of protein molecular dynamics with AI2BMD

Ran Bi, Xinheng He, Yatao Li, Jiawei Meng et al.
106 citations
Nature
Protein Structure and Dynamics
24.78
article

Ab initio characterization of protein molecular dynamics with AI2BMD

Ran Bi, Xinheng He, Yatao Li, Jiawei Meng, Haiguang Liu, Xiangzhen Shen, Chaoran Cheng, Mingyu Li, Tong Wang, Yusong Wang, Shaoning Li, Zun Wang, Bin Shao, He Zhang, Tie‐Yan Liu
article en
106 citations

Abstract

Biomolecular dynamics simulation is a fundamental technology for life sciences research, and its usefulness depends on its accuracy and efficiency<sup>1-3</sup>. Classical molecular dynamics simulation is fast but lacks chemical accuracy<sup>4,5</sup>. Quantum chemistry methods such as density functional theory can reach chemical accuracy but cannot scale to support large biomolecules<sup>6</sup>. Here we introduce an artificial intelligence-based ab initio biomolecular dynamics system (AI<sup>2</sup>BMD) that can efficiently simulate full-atom large biomolecules with ab initio accuracy. AI<sup>2</sup>BMD uses a protein fragmentation scheme and a machine learning force field<sup>7</sup> to achieve generalizable ab initio accuracy for energy and force calculations for various proteins comprising more than 10,000 atoms. Compared to density functional theory, it reduces the computational time by several orders of magnitude. With several hundred nanoseconds of dynamics simulations, AI<sup>2</sup>BMD demonstrated its ability to efficiently explore the conformational space of peptides and proteins, deriving accurate <sup>3</sup>J couplings that match nuclear magnetic resonance experiments, and showing protein folding and unfolding processes. Furthermore, AI<sup>2</sup>BMD enables precise free-energy calculations for protein folding, and the estimated thermodynamic properties are well aligned with experiments. AI<sup>2</sup>BMD could potentially complement wet-lab experiments, detect the dynamic processes of bioactivities and enable biomedical research that is impossible to conduct at present.

NatureVol. 635(8040)
Microsoft (United States) (US), Microsoft Research Asia (China) (CN)
Openalex Percentile: Top 0%
Protein Structure and Dynamics
24.78
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