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Biology subjects

Corbi-Verge, C.

Publications and source records attributed to Corbi-Verge, C..

2 recordsLinked to original sources

Designing real novel proteins using deep graph neural networks

Protein structure and function is determined by the arrangement of the linear sequence of amino acids in 3D space. Despite substantial advances, precisely designing sequences that fold into a predetermined shape (the "protein design" problem) remains difficult. We show that a deep graph neural network, ProteinSolver, can solve protein design by phrasing it as a constraint satisfaction problem (CSP). To sidestep the considerable issue of optimizing the network architecture, we first develop a network that is accurately able to solve the related and straightforward problem of Sudoku puzzles. Recognizing that each protein design CSP has many solutions, we train this network on millions of real protein sequences corresponding to thousands of protein structures. We show that our method rapidly designs novel protein sequences and perform a variety of in silico and in vitro validations suggesting that our designed proteins adopt the predetermined structures. One Sentence SummaryA neural network optimized using Sudoku puzzles designs protein sequences that adopt predetermined structures.

bioinformatics↗

A physics-based energy function allows the computational redesign of a PDZ domain

A powerful approach to understand protein structure and evolution is to perform computer simulations that mimic aspects of evolution. In particular, structure-based computational protein design (CPD) can address the inverse folding problem, exploring a large space of amino acid sequences and selecting ones predicted to adopt a given fold. Previously, CPD has been used to entirely redesign several proteins: all or most of the protein sequence was allowed to mutate freely; among sampled sequences, those with low computed folding energy were selected, and a few percent of them did indeed adopt the correct fold. Those studies used an energy function that was partly or largely knowledge-based, with several empirical terms. Here, we show that a PDZ domain can be entirely redesigned using a \"physics-based\" energy function that combines standard molecular mechanics and a recent, continuum electrostatic solvent model. Many thousands of sequences were generated by Monte Carlo simulation. Among the lowest-energy sequences, three were chosen for experimental testing. All three could be overexpressed and had native-like circular dichroism and 1D-NMR spectra. Two exhibited an increase in their thermal denaturation curves when a peptide ligand was present, indicating binding and suggesting correctly folded proteins. Evidently, the physical principles that govern molecular mechanics and continuum electrostatics are sufficient to perform whole-protein redesign. This is encouraging, since these methods provide physical insights, can be systematically improved, and are transferable to other biopolymers and ligands of medical or technological interest.\n\n\n\nO_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=73 SRC=\"FIGDIR/small/790667v3_ufig1.gif\" ALT=\"Figure 1\">\nView larger version (26K):\norg.highwire.dtl.DTLVardef@145ea28org.highwire.dtl.DTLVardef@10ffa2forg.highwire.dtl.DTLVardef@1f2460eorg.highwire.dtl.DTLVardef@d5691c_HPS_FORMAT_FIGEXP M_FIG Table of Contents Graphic\n\nC_FIG

biophysics↗