Development of a fluorescence-based assay for RecBCD activity using functional data analysis and design of experiments†

IF 3.1 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY RSC Chemical Biology Pub Date : 2025-03-17 DOI:10.1039/D4CB00291A
Adam Winnifrith, Steven R. Brown, Piotr Jedryszek, C. Grant, Philip E. Kay, Adam M. Thomas, Jacob D. Bradbury and Thomas Lanyon-Hogg
{"title":"Development of a fluorescence-based assay for RecBCD activity using functional data analysis and design of experiments†","authors":"Adam Winnifrith, Steven R. Brown, Piotr Jedryszek, C. Grant, Philip E. Kay, Adam M. Thomas, Jacob D. Bradbury and Thomas Lanyon-Hogg","doi":"10.1039/D4CB00291A","DOIUrl":null,"url":null,"abstract":"<p >Biochemical assays are essential tools in biological research and drug discovery, but optimisation of these assays is often a challenging and lengthy process due to the wide range of input variables and the complex effects of these variables on one another. Traditional ‘one-factor-at-a-time’ optimisation is both time-consuming and fails to explore the full range of input combinations. In contrast, the modern ‘design of experiments’ (DoE) approach enables simultaneous investigation of multiple input variables and their interactions, leading to more information-rich and efficient experimentation. We therefore sought to apply DoE to the optimisation of a new fluorescence-based assay for the enzyme RecBCD, a helicase–nuclease–ATPase complex involved in bacterial stress responses. A novel ‘functional data analysis’ (FDA) approach was used to predict the shape of RecBCD reaction curves in response to different combinations of input variables, which successfully identified assay conditions suitable for drug screening. Collectively, this work delivers a new assay for the antibiotic target RecBCD and demonstrates the potential of DoE and FDA to accelerate biochemical assay development.</p>","PeriodicalId":40691,"journal":{"name":"RSC Chemical Biology","volume":" 5","pages":" 772-779"},"PeriodicalIF":3.1000,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11955833/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC Chemical Biology","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/cb/d4cb00291a","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Biochemical assays are essential tools in biological research and drug discovery, but optimisation of these assays is often a challenging and lengthy process due to the wide range of input variables and the complex effects of these variables on one another. Traditional ‘one-factor-at-a-time’ optimisation is both time-consuming and fails to explore the full range of input combinations. In contrast, the modern ‘design of experiments’ (DoE) approach enables simultaneous investigation of multiple input variables and their interactions, leading to more information-rich and efficient experimentation. We therefore sought to apply DoE to the optimisation of a new fluorescence-based assay for the enzyme RecBCD, a helicase–nuclease–ATPase complex involved in bacterial stress responses. A novel ‘functional data analysis’ (FDA) approach was used to predict the shape of RecBCD reaction curves in response to different combinations of input variables, which successfully identified assay conditions suitable for drug screening. Collectively, this work delivers a new assay for the antibiotic target RecBCD and demonstrates the potential of DoE and FDA to accelerate biochemical assay development.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
利用功能数据分析和实验设计开发一种基于荧光的RecBCD活性测定方法。
生化分析是生物研究和药物发现的重要工具,但由于输入变量范围广,这些变量相互之间的复杂影响,这些分析的优化往往是一个具有挑战性和漫长的过程。传统的“一次一个因素”优化既耗时又无法探索输入组合的全部范围。相比之下,现代“实验设计”(DoE)方法能够同时调查多个输入变量及其相互作用,从而导致更丰富的信息和更有效的实验。因此,我们试图将DoE应用于优化一种新的基于荧光的酶RecBCD测定方法,RecBCD是一种参与细菌应激反应的解旋酶-核酸酶- atp酶复合物。采用一种新颖的“功能数据分析”(FDA)方法来预测不同输入变量组合下RecBCD反应曲线的形状,成功地确定了适合药物筛选的分析条件。总的来说,这项工作为抗生素靶点RecBCD提供了一种新的检测方法,并证明了DoE和FDA加速生化检测发展的潜力。
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 去求助
来源期刊
CiteScore
6.10
自引率
0.00%
发文量
128
审稿时长
10 weeks
期刊最新文献
Correction: Proteolysis targeting chimeras (PROTACs) come of age: entering the third decade of targeted protein degradation. An AKR1C3-activated kinase inhibitor prodrug. Tuning the efficiency of molecular probes via quinone methide-based in situ labeling. Backbone engineering in the hydrophobic core of villin headpiece. Contributors to the 2025 RSC Chemical Biology Emerging Investigators Collection.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1