A High-Throughput Fluorometric Assay for Lipid–Protein Binding

W. Cho, Y. Hu, K. Baek, H. Kim

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

2 Citations (Scopus)

Abstract

An increasing number of intracellular and extracellular proteins are shown to interact with membrane lipids under physiological conditions. For rapid and robust quantitative measurement of lipid–protein interaction, we developed a sensitive fluorescence quenching-based assay that is universally applicable to all proteins and lipids. The assay employs fluorescence protein (FP)-tagged proteins whose fluorescence emission intensity is decreased when they bind vesicles containing quenching lipids. This simple assay can be performed with a fluorescence plate reader or a spectrofluorometer and optimized for different proteins with various combinations of FPs and quenching lipids. The assay allows a rapid, sensitive, and accurate determination of lipid specificity and affinity for various lipid-binding proteins, and high-throughput screening of molecules that modulate their membrane binding.

Original languageEnglish
Title of host publicationMethods in Enzymology
PublisherAcademic Press Inc.
Pages1-18
Number of pages18
DOIs
Publication statusPublished - 2017

Publication series

NameMethods in Enzymology
Volume583
ISSN (Print)0076-6879
ISSN (Electronic)1557-7988

Bibliographical note

Publisher Copyright:
© 2017 Elsevier Inc.

Keywords

  • Dark quenchers
  • Fluorescence proteins
  • High-throughput fluorescence assay
  • Lipid specificity
  • Membrane protein binding
  • Membrane-binding inhibitors

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