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Method Article

Microscale Thermophoresis to Study Protein-Lipid Interactions in Solution

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July 8th, 2025

In This Article

Abstract

Source: Sparks, R. P. et al., Use of Microscale Thermophoresis to Measure Protein-Lipid Interactions. J. Vis. Exp. (2022)

This video demonstrates microscale thermophoresis for studying the protein-lipid interaction. The assay detects the interaction between molecules by quantifying the thermophoretic movement of fluorescent-labeled proteins in response to a temperature gradient. The fluorescent molecule is mixed with different concentrations of the non-fluorescent lipid molecules, and the mixture of molecules in the solution is loaded into capillaries. A temperature gradient is applied to the samples in the capillaries, and the movement of the fluorescent molecule in the temperature gradient is detected and recorded.

Protocol

1. Preparation of materials

  1. Prepare phosphate-buffered saline (PBS): 137 mM NaCl, 2.5 mM KCl, 10 mM NaH2PO4, and 2 mM KH2PO4, pH 7.4.
  2. Prepare NTA-Atto 647 N dye. Dilute stock NTA-Atto 647 N dye to 100 nM from a 100% DMSO solution into PBS without Tween.
  3. Express Vam7-His8 – Protein as a fusion protein in E. coli and purify it using Ni-NTA and size exclusion chromatography.
  4. Titrate the analyte in PBS buffer. If the analyte is in a different buffer, labeled MST is not particularly sensitive to minor buffer differences from molecules such as....

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Disclosures

No conflicts of interest declared.

Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Cy5 Maleimide Mono-Reactive DyeGE HealthcarePA23031For protein labeling
GraphPad PrismGraphPad software
Monolith NT.115 Capillaries (1000 count)NanotemperMO-K022Capillaries for MST
Monolith NT.115 machineNanotemperUniversity equipment
NTA-Atto 647 NSigma2175Label for His tags
Phosphatidylinositol 3-phosphate diC8 (PI(3)P diC8)EchelonP-3008Lipid for binding experiments

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