TY - JOUR
T1 - High-Throughput Approaches in Carbohydrate-Active Enzymology
T2 - Glycosidase and Glycosyl Transferase Inhibitors, Evolution, and Discovery
AU - Chao, L.
AU - Jongkees, S.
PY - 2019/9/9
Y1 - 2019/9/9
N2 - © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.Carbohydrates are attached and removed in living systems through the action of carbohydrate-active enzymes such as glycosyl transferases and glycoside hydrolases. The molecules resulting from these enzymes have many important roles in organisms, such as cellular communication, structural support, and energy metabolism. In general, each carbohydrate transformation requires a separate catalyst, and so these enzyme families are extremely diverse. To make this diversity manageable, high-throughput approaches look at many enzymes at once. Similarly, high-throughput approaches can be a powerful way of finding inhibitors that can be used to tune the reactivity of these enzymes, either in an industrial, a laboratory, or a medicinal setting. In this review, we provide an overview of how these enzymes and inhibitors can be sought using techniques such as high-throughput natural product and combinatorial library screening, phage and mRNA display of (glyco)peptides, fluorescence-activated cell sorting, and metagenomics.
AB - © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA.Carbohydrates are attached and removed in living systems through the action of carbohydrate-active enzymes such as glycosyl transferases and glycoside hydrolases. The molecules resulting from these enzymes have many important roles in organisms, such as cellular communication, structural support, and energy metabolism. In general, each carbohydrate transformation requires a separate catalyst, and so these enzyme families are extremely diverse. To make this diversity manageable, high-throughput approaches look at many enzymes at once. Similarly, high-throughput approaches can be a powerful way of finding inhibitors that can be used to tune the reactivity of these enzymes, either in an industrial, a laboratory, or a medicinal setting. In this review, we provide an overview of how these enzymes and inhibitors can be sought using techniques such as high-throughput natural product and combinatorial library screening, phage and mRNA display of (glyco)peptides, fluorescence-activated cell sorting, and metagenomics.
U2 - 10.1002/anie.201900055
DO - 10.1002/anie.201900055
M3 - Review article
VL - 58
SP - 12750
EP - 12760
JO - Angewandte Chemie. International Edition
JF - Angewandte Chemie. International Edition
SN - 1433-7851
IS - 37
ER -