Generalized biomolecular modeling and design with RoseTTAFold All-Atom

Rohith Krishna(University of Washington), Jue Wang(University of Washington), Woody Ahern(University of Washington), Pascal Sturmfels(University of Washington), Preetham Venkatesh(University of Washington), Indrek Kalvet(Howard Hughes Medical Institute), Gyu Rie Lee(Howard Hughes Medical Institute), Felix S. Morey-Burrows(University of Sheffield), Ivan Anishchenko(University of Washington), Ian R. Humphreys(University of Washington), Ryan McHugh(University of Washington), Dionne Vafeados(University of Washington), Xinting Li(University of Washington), George A. Sutherland(University of Sheffield), Andrew Hitchcock(University of Sheffield), C. Neil Hunter(University of Sheffield), Alex Kang(University of Washington), Evans Brackenbrough(University of Washington), Asim K. Bera(University of Washington), Minkyung Baek(Seoul National University), Frank DiMaio(University of Washington), David Baker(Howard Hughes Medical Institute)
Science
March 7, 2024
Cited by 836Open Access
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Abstract

Deep-learning methods have revolutionized protein structure prediction and design but are presently limited to protein-only systems. We describe RoseTTAFold All-Atom (RFAA), which combines a residue-based representation of amino acids and DNA bases with an atomic representation of all other groups to model assemblies that contain proteins, nucleic acids, small molecules, metals, and covalent modifications, given their sequences and chemical structures. By fine-tuning on denoising tasks, we developed RFdiffusion All-Atom (RFdiffusionAA), which builds protein structures around small molecules. Starting from random distributions of amino acid residues surrounding target small molecules, we designed and experimentally validated, through crystallography and binding measurements, proteins that bind the cardiac disease therapeutic digoxigenin, the enzymatic cofactor heme, and the light-harvesting molecule bilin.


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