化学
连接器
配体(生物化学)
高分辨率
垂钓
对接(动物)
仿形(计算机编程)
立体化学
组合化学
生物化学
色谱法
受体
渔业
遥感
医学
生物
操作系统
地质学
护理部
计算机科学
作者
Sileshi Gizachew Wubshet,Bing‐Rui Liu,Kenneth T. Kongstad,Ulrike Böcker,Malene Johanne Petersen,Tuo Li,Junru Wang,Dan Stærk
出处
期刊:Talanta
[Elsevier BV]
日期:2019-03-12
卷期号:200: 279-287
被引量:41
标识
DOI:10.1016/j.talanta.2019.03.047
摘要
Plants are well-recognized sources of inhibitors for α-glucosidase - a key target enzyme for management of type 2 diabetes. Recently, two advanced bioactivity-profiling techniques, i.e., ligand fishing and high-resolution inhibition profiling, have shown great promises for accelerating identification of α-glucosidase inhibitors from complex plant extracts. Non-specific affinities and non-specific inhibitions are major sources of false positive hits from ligand fishing and high-resolution inhibition profiling, respectively. In an attempt to minimize such false positive hits, we describe a new screening approach based on ligand fishing and high-resolution inhibition profiling for detection of high-affinity ligands and assessment of inhibitory activity, respectively. The complementary nature of ligand fishing and high-resolution inhibition profiling was explored to identify α-glucosidase inhibitory ligands from a complex mixture, and proof-of-concept was demonstrated with crude ethyl acetate extract of Ginkgo biloba. In addition to magnetic beads with a 3-carbon aliphatic linker, α-glucosidase was immobilized on magnetic beads with a 21-carbon aliphatic linker; and the two different types of magnetic beads were compared for their hydrolytic activity and fishing efficiency.
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