Suppr超能文献

用于定量高通量筛选的化合物管理

Compound Management for Quantitative High-Throughput Screening.

作者信息

Yasgar Adam, Shinn Paul, Jadhav Ajit, Auld Douglas, Michael Sam, Zheng Wei, Austin Christopher P, Inglese James, Simeonov Anton

机构信息

NIH Chemical Genomics Center, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892-3370, USA.

出版信息

JALA Charlottesv Va. 2008 Apr;13(2):79-89. doi: 10.1016/j.jala.2007.12.004.

Abstract

An efficient and versatile Compound Management operation is essential for the success of all downstream processes in high-throughput screening (HTS) and small molecule lead development. Staff, equipment, and processes need to be not only reliable, but remain flexible and prepared to incorporate paradigm changes. In the present report, we describe a system and associated processes which enable handling of compounds for both screening and follow-up purposes at the NIH Chemical Genomics Center (NCGC), a recently-established HTS and probe development center within the Molecular Libraries Initiative of the NIH Roadmap. Our screening process, termed quantitative HTS (qHTS), involves assaying the complete compound library, currently containing >200,000 members, at a series of dilutions to construct a full concentration-response profile. As such, Compound Management at the NCGC has been uniquely tasked to prepare, store, register, and track a vertically-developed plate dilution series (i.e., inter-plate titrations) in the 384-well format. These are compressed into a series of 1,536-well plates and are registered to track all subsequent plate storage. Here, we present details on the selection of equipment to enable automated, reliable and parallel compound manipulation in 384- and 1,536-well formats, protocols for preparation of inter-plate dilution series for qHTS, as well as qHTS-specific processes and issues.

摘要

高效且通用的化合物管理操作对于高通量筛选(HTS)和小分子先导物开发中所有下游流程的成功至关重要。人员、设备和流程不仅要可靠,还需保持灵活性,并准备好纳入范式变化。在本报告中,我们描述了一个系统及相关流程,该系统能够在美国国立卫生研究院(NIH)化学基因组学中心(NCGC)处理用于筛选和后续研究的化合物,NCGC是NIH路线图分子文库计划中最近设立的一个HTS和探针开发中心。我们的筛选过程称为定量HTS(qHTS),包括对目前包含超过20万个成员的完整化合物库进行一系列稀释测定,以构建完整的浓度 - 响应曲线。因此,NCGC的化合物管理承担了独特的任务,即制备、储存、登记和追踪384孔板格式的垂直开发的板稀释系列(即板间滴定)。这些被压缩成一系列1536孔板,并进行登记以追踪所有后续板的储存情况。在此,我们详细介绍了为实现384孔和1536孔格式的自动化、可靠且并行的化合物操作而选择的设备、用于qHTS的板间稀释系列制备方案,以及qHTS特定的流程和问题。

相似文献

1
Compound Management for Quantitative High-Throughput Screening.
JALA Charlottesv Va. 2008 Apr;13(2):79-89. doi: 10.1016/j.jala.2007.12.004.
2
A robotic platform for quantitative high-throughput screening.
Assay Drug Dev Technol. 2008 Oct;6(5):637-57. doi: 10.1089/adt.2008.150.
3
[Standard technical specifications for methacholine chloride (Methacholine) bronchial challenge test (2023)].
Zhonghua Jie He He Hu Xi Za Zhi. 2024 Feb 12;47(2):101-119. doi: 10.3760/cma.j.cn112147-20231019-00247.
4
Quantitative high-throughput screening: a titration-based approach that efficiently identifies biological activities in large chemical libraries.
Proc Natl Acad Sci U S A. 2006 Aug 1;103(31):11473-8. doi: 10.1073/pnas.0604348103. Epub 2006 Jul 24.
7
The future of toxicity testing: a focus on in vitro methods using a quantitative high-throughput screening platform.
Drug Discov Today. 2010 Dec;15(23-24):997-1007. doi: 10.1016/j.drudis.2010.07.007. Epub 2010 Aug 11.
9
MScreen: an integrated compound management and high-throughput screening data storage and analysis system.
J Biomol Screen. 2012 Sep;17(8):1080-7. doi: 10.1177/1087057112450186. Epub 2012 Jun 15.
10
HTS library plate rejuvenation using a DMSO-rich atmosphere.
SLAS Technol. 2024 Dec;29(6):100204. doi: 10.1016/j.slast.2024.100204. Epub 2024 Oct 11.

引用本文的文献

2
A general assay platform to study protein pharmacology using ligand-dependent structural dynamics.
Nat Commun. 2025 May 10;16(1):4342. doi: 10.1038/s41467-025-59658-6.
3
Machine Learning Models Identify Inhibitors of New Delhi Metallo-β-lactamase.
J Chem Inf Model. 2024 May 27;64(10):3977-3991. doi: 10.1021/acs.jcim.3c02015. Epub 2024 May 10.
5
Paracatalytic induction: Subverting specificity in hedgehog protein autoprocessing with small molecules.
Methods Enzymol. 2023;685:1-41. doi: 10.1016/bs.mie.2023.03.001. Epub 2023 Apr 19.
6
Quantitative Bioactivity Signatures of Dietary Supplements and Natural Products.
ACS Pharmacol Transl Sci. 2023 Apr 14;6(5):683-701. doi: 10.1021/acsptsci.2c00194. eCollection 2023 May 12.
7
In vivo quantitative high-throughput screening for drug discovery and comparative toxicology.
Dis Model Mech. 2023 Mar 1;16(3). doi: 10.1242/dmm.049863. Epub 2023 Mar 20.
9
A platform of assays for the discovery of anti-Zika small-molecules with activity in a 3D-bioprinted outer-blood-retina model.
PLoS One. 2022 Jan 18;17(1):e0261821. doi: 10.1371/journal.pone.0261821. eCollection 2022.
10
A Genome-Edited ERα-HiBiT Fusion Reporter Cell Line for the Identification of ERα Modulators High-Throughput Screening and CETSA.
Assay Drug Dev Technol. 2021 Nov-Dec;19(8):539-549. doi: 10.1089/adt.2021.059. Epub 2021 Oct 14.

本文引用的文献

1
Compound cytotoxicity profiling using quantitative high-throughput screening.
Environ Health Perspect. 2008 Mar;116(3):284-91. doi: 10.1289/ehp.10727.
2
Quantitative high-throughput screen identifies inhibitors of the Schistosoma mansoni redox cascade.
PLoS Negl Trop Dis. 2008 Jan 2;2(1):e127. doi: 10.1371/journal.pntd.0000127.
3
Three classes of glucocerebrosidase inhibitors identified by quantitative high-throughput screening are chaperone leads for Gaucher disease.
Proc Natl Acad Sci U S A. 2007 Aug 7;104(32):13192-7. doi: 10.1073/pnas.0705637104. Epub 2007 Aug 1.
4
Reporting data from high-throughput screening of small-molecule libraries.
Nat Chem Biol. 2007 Aug;3(8):438-41. doi: 10.1038/nchembio0807-438.
5
Mixing in 384-well plates: issues, measurements, and solutions.
Assay Drug Dev Technol. 2007 Apr;5(2):265-75. doi: 10.1089/adt.2006.042.
6
Leadlikeness and structural diversity of synthetic screening libraries.
Mol Divers. 2006 Aug;10(3):377-88. doi: 10.1007/s11030-006-9040-6. Epub 2006 Sep 21.
7
Quality assessment and analysis of Biogen Idec compound library.
J Biomol Screen. 2006 Oct;11(7):828-35. doi: 10.1177/1087057106290993. Epub 2006 Sep 6.
8
Quantitative high-throughput screening: a titration-based approach that efficiently identifies biological activities in large chemical libraries.
Proc Natl Acad Sci U S A. 2006 Aug 1;103(31):11473-8. doi: 10.1073/pnas.0604348103. Epub 2006 Jul 24.
9
Statistical practice in high-throughput screening data analysis.
Nat Biotechnol. 2006 Feb;24(2):167-75. doi: 10.1038/nbt1186.
10
Assessing the minimum number of data points required for accurate IC50 determination.
Assay Drug Dev Technol. 2005 Oct;3(5):525-31. doi: 10.1089/adt.2005.3.525.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验