Design and Screening Strategies for α-Glucosidase Inhibitors Based on Enzymological Information

被引:75
作者
Hakamata, Wataru [1 ]
Kurihara, Masaaki
Okuda, Haruhiro
Nishio, Toshiyuki [1 ]
Oku, Tadatake [1 ]
机构
[1] Nihon Univ, Coll Bioresource Sci, Dept Biol Chem, Tokyo 102, Japan
关键词
alpha-glucosidase; substrate specificity; inhibitor; HTS; virtual screening; in silico; structure based drug design; HEPATITIS-C VIRUS; GLYCOSIDASE INHIBITORS; CHEMOTHERAPEUTIC VALUE; QUALITY-CONTROL; SUBSTRATE-SPECIFICITY; HYDROLYTIC ACTIVITY; NATURAL OCCURRENCE; DEOXY DERIVATIVES; ANOMERIC FORMS; GLYCOSYLATION;
D O I
10.2174/156802609787354306
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
alpha-Glucosidase inhibitors are marketed as therapeutic drugs for diabetes that act through the inhibition of carbohydrate metabolism. Inhibitors of the alpha-glucosidases that are involved in the biosynthesis of N-linked oligosaccharide chains have been reported to have antitumor, antiviral, and apoptosis-inducing activities, and some have been used clinically. alpha-Glucosidase inhibitors have interesting biological activities, and their design, synthesis, and screening are being actively performed. In quite a few reports, however, alpha-glucosidases with different origins than the target alpha-glucosidases, have been used to evaluate inhibitory activities. There might be confusion regarding the naming of alpha-glucosidases. For example, the term alpha-glucosidase is sometimes used as a generic name for alpha-glucoside hydrolases. Moreover, IUBMB recommends the use of "alpha-glucosidase" (EC 3.2.1.20) for exo-alpha-1,4-glucosidases, which are further classified into four families based on amino acid sequence similarities. Accordingly, substrate specificity and susceptibility to inhibitors varies markedly among enzymes in the IUBMB alpha-glucosidases. The design and screening of inhibitors without consideration of these differences is not efficient. For the development of a practical inhibitor that is operational in cells, HTS using the target alpha-glucosidase and the computer-aided design of inhibitors based on enzymatic information concerning the same alpha-glucosidase are essential.
引用
收藏
页码:3 / 12
页数:10
相关论文
共 112 条
[1]  
*ACC INC, ACC DISC STUD
[2]  
Alymova I. V., 2005, Current Drug Targets - Infectious Disorders, V5, P401, DOI 10.2174/156800505774912884
[3]   Sugar-mimic glycosidase inhibitors: natural occurrence, biological activity and prospects for therapeutic application [J].
Asano, N ;
Nash, RJ ;
Molyneux, RJ ;
Fleet, GWJ .
TETRAHEDRON-ASYMMETRY, 2000, 11 (08) :1645-1680
[4]  
ATSUMI S, 1993, CANCER RES, V53, P4896
[5]   Integration of virtual and high-throughput screening [J].
Bajorath, F .
NATURE REVIEWS DRUG DISCOVERY, 2002, 1 (11) :882-894
[6]   PURIFICATION AND CHARACTERIZATION OF TRIMMING GLUCOSIDASE-I FROM PIG-LIVER [J].
BAUSE, E ;
SCHWEDEN, J ;
GROSS, A ;
ORTHEN, B .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1989, 183 (03) :661-669
[7]   Chemical glycobiology [J].
Bertozzi, CR ;
Kiessling, LL .
SCIENCE, 2001, 291 (5512) :2357-2364
[8]   Binding mode analyses and pharmacophore model development for sulfonamide chalcone derivatives, a new class of α-glucosidase inhibitors [J].
Bharatham, Kavitha ;
Bharatham, Nagakumar ;
Park, Ki Hun ;
Lee, Keun Woo .
JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 2008, 26 (08) :1202-1212
[9]  
*BIOINF RES CTR, MOL SOFTW
[10]   Molecular chaperones and protein quality control [J].
Bukau, Bernd ;
Weissman, Jonathan ;
Horwich, Arthur .
CELL, 2006, 125 (03) :443-451