1. Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710, USA

Correspondence to: Homme W. Hellinga Correspondence and requests for material should be addressed to H.W.H. (Email: hwh@biochem.duke.edu).

Abstract

The formation of complexes between proteins and ligands is fundamental to biological processes at the molecular level. Manipulation of molecular recognition between ligands and proteins is therefore important for basic biological studies¹ and has many biotechnological applications, including the construction of enzymes^{2, 3, 4}, biosensors^{5, 6}, genetic circuits⁷, signal transduction pathways⁸ and chiral separations⁹. The systematic manipulation of binding sites remains a major challenge. Computational design offers enormous generality for engineering protein structure and function¹⁰. Here we present a structure-based computational method that can drastically redesign protein ligand-binding specificities. This method was used to construct soluble receptors that bind trinitrotoluene, l-lactate or serotonin with high selectivity and affinity. These engineered receptors can function as biosensors for their new ligands; we also incorporated them into synthetic bacterial signal transduction pathways, regulating gene expression in response to extracellular trinitrotoluene or l-lactate. The use of various ligands and proteins shows that a high degree of control over biomolecular recognition has been established computationally. The biological and biosensing activities of the designed receptors illustrate potential applications of computational design.

1. Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710, USA

Correspondence to: Homme W. Hellinga Correspondence and requests for material should be addressed to H.W.H. (Email: hwh@biochem.duke.edu).