General theory of specific binding: insights from a genetic-mechano-chemical protein model

TL;DR

This paper introduces a comprehensive model integrating chemistry, mechanics, and genetics to explain how proteins evolve high specificity in binding, highlighting the importance of size, flexibility, and correlated mutations for molecular discrimination.

Contribution

It presents a novel, general theory of specific protein binding that accounts for the evolution of high specificity through structural and genetic mechanisms.

Findings

Larger proteins are more capable of achieving complex discrimination tasks.

Correlated mutations extend beyond binding sites to enhance specificity.

Flexibility and shape mismatch influence discrimination effectiveness.

Abstract

Proteins need to selectively interact with specific targets among a multitude of similar molecules in the cell. But despite a firm physical understanding of binding interactions, we lack a general theory of how proteins evolve high specificity. Here, we present such a model that combines chemistry, mechanics and genetics, and explains how their interplay governs the evolution of specific protein-ligand interactions. The model shows that there are many routes to achieving molecular discrimination - by varying degrees of flexibility and shape/chemistry complementarity - but the key ingredient is precision. Harder discrimination tasks require more collective and precise coaction of structure, forces and movements. Proteins can achieve this through correlated mutations extending far from a binding site, which fine-tune the localized interaction with the ligand. Thus, the solution of more complicated tasks is enabled by increasing the protein size, and proteins become more evolvable and robust when they are larger than the bare minimum required for discrimination. The model makes testable, specific predictions about the role of flexibility and shape mismatch in discrimination, and how evolution can independently tune affinity and specificity. Thus, the proposed theory of specific binding addresses the natural question of "why are proteins so big?". A possible answer is that molecular discrimination is often a hard task best performed by adding more layers to the protein.