Journal Article

Reactibodies generated by kinetic selection couple chemical reactivity with favorable protein dynamics

Ponomarenko, Natalia, Smirnov, Ivan, Tramontano, Alfonso, Débat, Hélène, Kurkova, Inna, Reshetnyak, Andrey, Gabibov, Alexander, Friboulet, Alain, Kuznetsov, Nikita, Carletti, Eugénie, Nachon, Florian, Avalle, Bérangère, Tonevitsky, Alexander G, Belogurov, Alexey A. Jr, Masson, Patrick, Nicolet, Yvain, Mitkevich, Vladimir A, Makarov, Alexander A

2011

Overview

Igs offer a versatile template for combinatorial and rational design approaches to the de novo creation of catalytically active proteins. We have used a covalent capture selection strategy to identify biocatalysts from within a human semisynthetic antibody variable fragment library that uses a nucleophilic mechanism. Specific phosphonylation at a single tyrosine within the variable light-chain framework was confirmed in a recombinant IgG construct. High-resolution crystallographic structures of unmodified and phosphonylated Fabs display a 15-Å-deep two-chamber cavity at the interface of variable light (VL) and variable heavy (VH) fragments having a nucleophilic tyrosine at the base of the site. The depth and structure of the pocket are atypical of antibodies in general but can be compared qualitatively with the catalytic site of cholinesterases. A structurally disordered heavy chain complementary determining region 3 loop, constituting a wall of the cleft, is stabilized after covalent modification by hydrogen bonding to the phosphonate tropinol moiety. These features and presteady state kinetics analysis indicate that an induced fit mechanism operates in this reaction. Mutations of residues located in this stabilized loop do not interfere with direct contacts to the organophosphate ligand but can interrogate second shell interactions, because the H3 loop has a conformation adjusted for binding. Kinetic and thermodynamic parameters along with computational docking support the active site model, including plasticity and simple catalytic components. Although relatively uncomplicated, this catalytic machinery displays both stereo- and chemical selectivity. The organophosphate pesticide paraoxon is hydrolyzed by covalent catalysis with rate-limiting dephosphorylation. This reactibody is, therefore, a kinetically selected protein template that has enzyme-like catalytic attributes.

• Publisher: National Academy of Sciences,National Acad Sciences
• Subject: Active sites / Algorithms / Amino Acid Sequence / Animals / Antibodies / Antibodies - chemistry / Antibodies - genetics / Antibodies - metabolism / Binding sites / Binding Sites - genetics / Biological Sciences / Calorimetry / Catalysis / catalytic activity / Chemical reactions / CHO Cells / Complementarity Determining Regions - chemistry / Complementarity Determining Regions - genetics / Complementarity Determining Regions - metabolism / Cricetinae / Cricetulus / Crystallography, X-Ray / dephosphorylation / Enzyme kinetics / Enzymes / Esters / Humans / hydrogen bonding / immunoglobulin G / Immunoglobulin Light Chains - chemistry / Immunoglobulin Light Chains - genetics / Immunoglobulin Light Chains - metabolism / Immunoglobulin Variable Region - chemistry / Immunoglobulin Variable Region - genetics / Immunoglobulin Variable Region - metabolism / Kinetics / Ligands / light intensity / Models, Molecular / Molecular Sequence Data / Molecules / Mutation / Organophosphates / Organophosphorus pesticides / paraoxon / Pesticides / Phosphonic acids / Protein Binding / Protein Conformation / Proteins / Proteins - chemistry / Proteins - genetics / Proteins - metabolism / Reactivity / Recombinant Proteins - chemistry / Recombinant Proteins - metabolism / Spectrometry, Mass, Electrospray Ionization / Thermodynamics / tyrosine