Literature DB >> 19822881

Review article: high-throughput affinity-based technologies for small-molecule drug discovery.

Zhengrong Zhu1, John Cuozzo.   

Abstract

High-throughput affinity-based technologies are rapidly growing in use as primary screening methods in drug discovery. In this review, their principles and applications are described and their impact on small-molecule drug discovery is evaluated. In general, these technologies can be divided into 2 groups: those that detect binding interactions by measuring changes to the protein target and those that detect bound compounds. Technologies detecting binding interactions by focusing on the protein have limited throughput but can reveal mechanistic information about the binding interaction; technologies detecting bound compounds have very high throughput, some even significantly higher than current high-throughput screening technologies, but offer limited information about the binding interaction. In addition, the appropriate use of affinity-based technologies is discussed. Finally, nanotechnology is predicted to generate a significant impact on the future of affinity-based technologies.

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Year:  2009        PMID: 19822881     DOI: 10.1177/1087057109350114

Source DB:  PubMed          Journal:  J Biomol Screen        ISSN: 1087-0571


  11 in total

1.  Analysis of high-throughput screening assays using cluster enrichment.

Authors:  Minya Pu; Tomoko Hayashi; Howard Cottam; Joseph Mulvaney; Michelle Arkin; Maripat Corr; Dennis Carson; Karen Messer
Journal:  Stat Med       Date:  2012-07-05       Impact factor: 2.373

2.  Stereo- and regiodefined DNA-encoded chemical libraries enable efficient tumour-targeting applications.

Authors:  Nicholas Favalli; Gabriele Bassi; Christian Pellegrino; Jacopo Millul; Roberto De Luca; Samuele Cazzamalli; Su Yang; Anika Trenner; Nour L Mozaffari; Renier Myburgh; Mustafa Moroglu; Stuart J Conway; Alessandro A Sartori; Markus G Manz; Richard A Lerner; Peter K Vogt; Jörg Scheuermann; Dario Neri
Journal:  Nat Chem       Date:  2021-04-08       Impact factor: 24.427

Review 3.  Small-molecule discovery from DNA-encoded chemical libraries.

Authors:  Ralph E Kleiner; Christoph E Dumelin; David R Liu
Journal:  Chem Soc Rev       Date:  2011-06-14       Impact factor: 54.564

4.  Accelerating the Throughput of Affinity Mass Spectrometry-Based Ligand Screening toward a G Protein-Coupled Receptor.

Authors:  Yan Lu; Shanshan Qin; Bingjie Zhang; Antao Dai; Xiaoqing Cai; Mengna Ma; Zhan-Guo Gao; Dehua Yang; Raymond C Stevens; Kenneth A Jacobson; Ming-Wei Wang; Wenqing Shui
Journal:  Anal Chem       Date:  2019-06-12       Impact factor: 6.986

Review 5.  Targeting the undruggable proteome: the small molecules of my dreams.

Authors:  Craig M Crews
Journal:  Chem Biol       Date:  2010-06-25

6.  Interaction-dependent PCR: identification of ligand-target pairs from libraries of ligands and libraries of targets in a single solution-phase experiment.

Authors:  Lynn M McGregor; David J Gorin; Christoph E Dumelin; David R Liu
Journal:  J Am Chem Soc       Date:  2010-11-10       Impact factor: 15.419

7.  Exploiting ligand-protein conjugates to monitor ligand-receptor interactions.

Authors:  Hirohito Haruki; Monica Rengifo Gonzalez; Kai Johnsson
Journal:  PLoS One       Date:  2012-05-31       Impact factor: 3.240

8.  A Library Screening Strategy Combining the Concepts of MS Binding Assays and Affinity Selection Mass Spectrometry.

Authors:  Jürgen Gabriel; Georg Höfner; Klaus T Wanner
Journal:  Front Chem       Date:  2019-10-04       Impact factor: 5.221

Review 9.  Novel selection methods for DNA-encoded chemical libraries.

Authors:  Alix I Chan; Lynn M McGregor; David R Liu
Journal:  Curr Opin Chem Biol       Date:  2015-02-24       Impact factor: 8.822

Review 10.  Emerging Screening Approaches in the Development of Nrf2-Keap1 Protein-Protein Interaction Inhibitors.

Authors:  Chung-Hang Leung; Jia-Tong Zhang; Guan-Jun Yang; Hao Liu; Quan-Bin Han; Dik-Lung Ma
Journal:  Int J Mol Sci       Date:  2019-09-10       Impact factor: 5.923

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