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High-throughput and Comprehensive Drug Surveillance Using Multisegment Injection-Capillary Electrophoresis-Mass Spectrometry
Published on: April 23, 2019
High-throughput investigation of macromolecular interactions for drug development using spectral shift technology
Charlotte E Hunter1, Ehmke Pohl1,2, Stefanie Freitag-Pohl1
1Department of Chemistry, Durham University, South Road, Durham, DH1 3LE UK.
Spectral shift analysis offers a powerful, label-free method for studying macromolecular interactions. This review highlights its utility in drug discovery, particularly with high-throughput screening platforms like NanoTemper
Area of Science:
- Biophysics
- Biochemistry
- Drug Discovery
Background:
- Macromolecular interactions are crucial in biological processes and drug development.
- Biophysical methods are essential for characterizing these interactions.
- Spectral shift analysis is a valuable technique for studying binding events.
Purpose of the Study:
- To review spectral shift analysis as a tool for studying macromolecular interactions.
- To position spectral shift analysis within the landscape of biophysical methods.
- To discuss its application in drug discovery, including high-throughput screening.
Main Methods:
- Focuses on spectral shift analysis.
- Introduces NanoTemper's Dianthus platform for high-throughput screening.
- Mentions orthogonal methods like temperature-related intensity change (TRIC) and fluorescent labeling techniques.
Main Results:
- Dianthus platform enables mass-independent, immobilization-free screening.
- Spectral shift and TRIC methods are effective for various binding partners.
- Practical tips for spectral shift methods are provided.
Conclusions:
- Spectral shift analysis is a versatile tool for characterizing macromolecular interactions.
- The Dianthus platform enhances high-throughput screening capabilities in drug discovery.
- Spectral shift methods have significant current and future applications in drug discovery processes.
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