Information-Rich Drug Discovery Enabled by Next-Generation Multiplexing SPR

ZÁZNAM | Proběhlo St, 20.3.2024
Na tomto webináři se dozvíte, jak lze metodu SPR multiplexovat a automatizovat, aby bylo možné provádět vysoce výkonný screening kandidátů na léčiva s velkým množstvím dat proti více cílovým proteinům.
Technology Networks: Information-Rich Drug Discovery Enabled by Next-Generation Multiplexing SPR
Technology Networks: Information-Rich Drug Discovery Enabled by Next-Generation Multiplexing SPR

Detailed validation is key in successful drug development. Surface plasmon resonance (SPR) offers a label-free, direct-binding analysis that brings additional insights into drug kinetics compared to established functional assays.

SPR gives detailed information on affinity, complex half-life, thermodynamic constants and mode-of-action of potential candidates.

In this webinar, you’ll discover how SPR can be multiplexed and automated to enable high-throughput, data-rich drug candidate screening against multiple target proteins.

Attend this webinar to discover:

  • The relevance of kinetics and SPR for your drug development project
  • The value of multiplexing assays for drug development
  • Bruker’s newest Triceratops SPR #64, its flexibility and throughput in drug discovery and development pipelines

Presenter: Dr. Cyrill George Brunner (Senior Application Specialist, Bruker Daltonics)

Technology Networks
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