NGS data from: Deploying synthetic coevolution and machine learning to engineer protein-protein interactions
Fine-tuning of protein-protein interactions occurs naturally through coevolution, but this process is difficult to recapitulate in the laboratory. We describe a synthetic platform for protein-protein coevolution that can isolate matched pairs of interacting muteins from complex libraries. This large...
Gespeichert in:
Hauptverfasser: | , , , , , , , , , , |
---|---|
Format: | Dataset |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Fine-tuning of protein-protein interactions occurs naturally through
coevolution, but this process is difficult to recapitulate in the
laboratory. We describe a synthetic platform for 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 pre-trained 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
generating protein complexes with diverse molecular recognition properties
as tools for biotechnology and synthetic biology. |
---|---|
DOI: | 10.5061/dryad.gf1vhhmv7 |