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From sequence to function through structure: Deep learning for protein design.
Ferruz, Noelia; Heinzinger, Michael; Akdel, Mehmet; Goncearenco, Alexander; Naef, Luca; Dallago, Christian.
Afiliación
  • Ferruz N; Institute of Informatics and Applications, University of Girona, Girona, Spain.
  • Heinzinger M; Department of Biochemistry, University of Bayreuth, Bayreuth, Germany.
  • Akdel M; Department of Informatics, Bioinformatics & Computational Biology, Technische Universität München, 85748 Garching, Germany.
  • Goncearenco A; VantAI, 151 W 42nd Street, New York, NY 10036, United States.
  • Naef L; VantAI, 151 W 42nd Street, New York, NY 10036, United States.
  • Dallago C; VantAI, 151 W 42nd Street, New York, NY 10036, United States.
Comput Struct Biotechnol J ; 21: 238-250, 2023.
Article en En | MEDLINE | ID: mdl-36544476
The process of designing biomolecules, in particular proteins, is witnessing a rapid change in available tooling and approaches, moving from design through physicochemical force fields, to producing plausible, complex sequences fast via end-to-end differentiable statistical models. To achieve conditional and controllable protein design, researchers at the interface of artificial intelligence and biology leverage advances in natural language processing (NLP) and computer vision techniques, coupled with advances in computing hardware to learn patterns from growing biological databases, curated annotations thereof, or both. Once learned, these patterns can be used to provide novel insights into mechanistic biology and the design of biomolecules. However, navigating and understanding the practical applications for the many recent protein design tools is complex. To facilitate this, we 1) document recent advances in deep learning (DL) assisted protein design from the last three years, 2) present a practical pipeline that allows to go from de novo-generated sequences to their predicted properties and web-powered visualization within minutes, and 3) leverage it to suggest a generated protein sequence which might be used to engineer a biosynthetic gene cluster to produce a molecular glue-like compound. Lastly, we discuss challenges and highlight opportunities for the protein design field.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Comput Struct Biotechnol J Año: 2023 Tipo del documento: Article País de afiliación: España Pais de publicación: Países Bajos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Comput Struct Biotechnol J Año: 2023 Tipo del documento: Article País de afiliación: España Pais de publicación: Países Bajos