Sensitive colorimetric assays for α-glucosidase activity and inhibitor screening based on unmodified gold nanoparticles

被引:38
|
作者
Chen, Hongxia [1 ]
Zhang, Jiangjiang [1 ]
Wu, Heng [1 ]
Koh, Kwangnak [2 ]
Yin, Yongmei [3 ]
机构
[1] Shanghai Univ, Sch Life Sci, Lab Biosensing Technol, Shanghai 200444, Peoples R China
[2] Pusan Natl Univ, Inst Gen Educ, Pusan 609735, South Korea
[3] Nanjing Med Univ, Affiliated Hosp 5, Dept Oncol, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Colorimetric biosensor; Gold nanoparticle; alpha-Glucosidase; Inhibitor; TYPE-2; DIABETES-MELLITUS; IN-VIVO; AU NANOPARTICLES; AMYLASE ACTIVITY; CONTROLLED-TRIAL; GRAPHENE OXIDE; DNA DETECTION; SENSOR; CYSTEINE; AGGREGATION;
D O I
10.1016/j.aca.2015.02.022
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A colorimetric sensor has been developed in this work to sensitively detect alpha-glucosidase activity and screen alpha-glucosidase inhibitors (AGIs) utilizing unmodified gold nanoparticles (AuNPs). The sensing strategy is based on triple-catalytic reaction triggered by alpha-glucosidase. In the presence of alpha-glucosidase, aggregation of AuNPs is prohibited due to the oxidation of cysteine to cystine in the system. However, with addition of AGIs, cysteine induced aggregation of AuNPs occurs. Thus, a new method for alpha-glucosidase activity detection and AGIs screening is developed by measuring the UV-vis absorption or visually distinguishing. A well linear relation is presented in a range of 0.0025-0.05 U mL(-1). The detection limit is found to be 0.001 U mL(-1) for alpha-glucosidase assay, which is one order of magnitude lower than other reports. The IC50 values of four kinds of inhibitors observed with this method are in accordance with other reports. The using of unmodified AuNPs in this work avoids the complicated and time-consuming modification procedure. This simple and efficient colorimetric method can also be extended to other enzymes assays. (C) 2015 Published by Elsevier B.V.
引用
收藏
页码:92 / 98
页数:7
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