Deploying synthetic coevolution and machine learning to engineer protein-protein interactions

Author:

Yang Aerin1ORCID,Jude Kevin M.12ORCID,Lai Ben3,Minot Mason4ORCID,Kocyla Anna M.1ORCID,Glassman Caleb R.1ORCID,Nishimiya Daisuke1ORCID,Kim Yoon Seok1ORCID,Reddy Sai T.4ORCID,Khan Aly A.35ORCID,Garcia K. Christopher126ORCID

Affiliation:

1. Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA 94305, USA.

2. Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.

3. Toyota Technological Institute at Chicago, Chicago, IL 60637, USA.

4. Department of Biosystems Science and Engineering, ETH Zurich, Basel, Switzerland.

5. Departments of Pathology and Family Medicine, University of Chicago, Chicago, IL 60637, USA.

6. Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.

Abstract

Fine-tuning of protein-protein interactions occurs naturally through coevolution, but this process is difficult to recapitulate in the laboratory. We describe a platform for synthetic protein-protein coevolution that can isolate matched pairs of interacting muteins from complex libraries. This large dataset of coevolved complexes drove a systems-level analysis of molecular recognition between Z domain–affibody pairs spanning a wide range of structures, affinities, cross-reactivities, and orthogonalities, and captured a broad spectrum of coevolutionary networks. Furthermore, we harnessed pretrained protein language models to expand, in silico, the amino acid diversity of our coevolution screen, predicting remodeled interfaces beyond the reach of the experimental library. The integration of these approaches provides a means of simulating protein coevolution and generating protein complexes with diverse molecular recognition properties for biotechnology and synthetic biology.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference68 articles.

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