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© Research
Publication : ACS Catalysis

Computer-aided design of sequence libraries for the engineering of transglucosylase binding subsites to enable glucosylation of an unnatural disaccharide motif of relevance for bacterial antigen synthesis

Scientific Fields
Diseases
Organisms
Applications
Technique

Published in ACS Catalysis - 07 Jan 2015

Vergès A, Cambon E, Barbe S, Salamone S, Le Guen Y, Moulis C, Mulard LA, Remaud-Siméon M, André I

ACS Catalysis 2015, 5, 1186-98

The exploration of chemo-enzymatic routes to complex carbohydrates has been hampered by the lack of appropriate enzymatic tools having the substrate specificity for new reactions. Here, we used a computer-aided design framework to guide the construction of a small, diversity-controlled library of amino acid sequences of an α-transglucosylase, the sugar binding subsites of which were re-engineered to enable the challenging 1,2-cis-glucosylation of a partially protected β-linked disaccharide allyl (2-deoxy-2-trichloroacetamido-β-D-glucopyranosyl)-(1→2)-α-L-rhamnopyranoside, a potential intermediate in the synthesis of Shigella flexneri cell-surface oligosaccharides. The target disaccharide is not recognized by the parental wild-type enzyme and exhibits a molecular structure very distinct from that of the natural α-(1→4)-linked acceptor. A profound reshaping of the binding pocket had thus to be performed. Following the selection of 23 amino acid positions from the first shell, mutations were sampled using RosettaDesign leading to a subset of 1515 designed sequences, which were further analyzed by determining the amino acid variability among the designed sequences and their conservation in evolutionary-related enzymes. A combinatorial library of 2.7 × 104 variants was finally designed, constructed, and screened. One mutant showing the desired and totally new specificity was successfully identified from this first round of screening. Impressively, this mutant contained seven substitutions in the first shell of the active site leading to a drastic reshaping of the catalytic pocket without significantly perturbing the original specificity for sucrose donor substrate. This work illustrates how computer-aided approaches can undoubtedly offer novel opportunities to
design tailored carbohydrate-active enzymes of interest for glycochemistry or synthetic glycobiology.