Detection of Small-Molecule Aggregation with High-Throughput Microplate Biophysical Methods

Q3 Biochemistry, Genetics and Molecular Biology
Samantha J. Allen, Corey M. Dower, Annie X. Liu, Kevin J. Lumb
{"title":"Detection of Small-Molecule Aggregation with High-Throughput Microplate Biophysical Methods","authors":"Samantha J. Allen,&nbsp;Corey M. Dower,&nbsp;Annie X. Liu,&nbsp;Kevin J. Lumb","doi":"10.1002/cpch.78","DOIUrl":null,"url":null,"abstract":"<p>Small-molecule drug discovery can be hindered by the formation of aggregates that act as non-selective inhibitors of drug targets. Such aggregates appear as false positives in high-throughput screening campaigns and can bedevil structure-activity relationships during compound optimization. Protocols are described for resonant waveguide grating (RWG) and dynamic light scattering (DLS) as microplate-based high-throughput approaches to identify compound aggregation. Resonant waveguide grating and dynamic light scattering give equivalent results for the compound test set, as assessed with Bland-Altman analysis. © 2019 The Authors.</p><p><b>Basic Protocol 1</b>: Resonant waveguide grating (RWG) in 384-well or 1536-well plate format to detect compound aggregation</p><p><b>Basic Protocol 2</b>: Dynamic light scattering (DLS) in 384-well plate format to detect compound aggregation</p>","PeriodicalId":38051,"journal":{"name":"Current protocols in chemical biology","volume":"12 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-03-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpch.78","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current protocols in chemical biology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpch.78","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 3

Abstract

Small-molecule drug discovery can be hindered by the formation of aggregates that act as non-selective inhibitors of drug targets. Such aggregates appear as false positives in high-throughput screening campaigns and can bedevil structure-activity relationships during compound optimization. Protocols are described for resonant waveguide grating (RWG) and dynamic light scattering (DLS) as microplate-based high-throughput approaches to identify compound aggregation. Resonant waveguide grating and dynamic light scattering give equivalent results for the compound test set, as assessed with Bland-Altman analysis. © 2019 The Authors.

Basic Protocol 1: Resonant waveguide grating (RWG) in 384-well or 1536-well plate format to detect compound aggregation

Basic Protocol 2: Dynamic light scattering (DLS) in 384-well plate format to detect compound aggregation

Abstract Image

高通量微孔板生物物理方法检测小分子聚集
小分子药物的发现可能会被聚集物的形成所阻碍,这些聚集物作为药物靶点的非选择性抑制剂。这种聚合体在高通量筛选活动中出现假阳性,并可能在化合物优化过程中困扰结构-活性关系。描述了共振波导光栅(RWG)和动态光散射(DLS)作为基于微板的高通量方法来识别化合物聚集的协议。谐振波导光栅和动态光散射对复合测试集给出了等效的结果,用Bland-Altman分析进行了评估。©2019作者。基本协议1:384孔或1536孔板格式的谐振波导光栅(RWG)检测化合物聚集基本协议2:384孔板格式的动态光散射(DLS)检测化合物聚集
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Current protocols in chemical biology
Current protocols in chemical biology Biochemistry, Genetics and Molecular Biology-Biophysics
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信