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一种快速定量荧光方法蛋白靶向小分子药物筛选
JoVE Journal
Bioengenharia
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JoVE Journal Bioengenharia
A Rapid and Quantitative Fluorimetric Method for Protein-Targeting Small Molecule Drug Screening
DOI:

08:34 min

October 16, 2015

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Capítulos

  • 00:05Título
  • 01:05Synthesis of Protein-templated Gold Nanoclusters (Au NCs)
  • 03:17Screen Relative Binding Affinity of Different Small Molecular Drugs to HSA
  • 05:19Measure the Binding Constant of a Specific Drug to HSA
  • 06:41Results: Studying Protein-drug Binding by Forming Fluorescent Gold Nanoclusters (Au NCs) using Drug-loaded Serum Albumen as Template
  • 07:53Conclusion

Summary

Tadução automática

A protocol for small molecular drug screening based on in-situ synthesis of ultrasmall fluorescent gold nanoclusters (Au NCs) using drug-loaded protein as template is presented. This method is simple to determine the binding affinity of drugs to a target protein by a visible fluorescent signal emitted from the protein-templated Au NCs.

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