Quantitative Flow Cytometry to Study Labeled Protein-Phospholipid Vesicle Interactions

Abstract

Source: Podoplelova, N. et al., Analyzing the Interaction of Fluorescent-Labeled Proteins with Artificial Phospholipid Microvesicles using Quantitative Flow Cytometry. J. Vis. Exp. (2022)

In this video, we demonstrate the interaction between proteins and artificial phospholipid vesicles using quantitative flow cytometry. The binding of fluorescently-labeled proteins to fluorescently-labeled phospholipid vesicles increases the mean fluorescence intensity, and this increase is detected by a flow cytometer.

Protocol

1. Detection of protein-lipid interaction by flow cytometry Kinetic binding experiments Dilute phospholipid vesicles in Tyrode's buffer (20 mM HEPES, 150 mM NaCl, 2.7 mM KCl, 1 mM MgCl2, 0.4 mM NaH2PO4, 2.5 mM CaCl2, 5 mM glucose, 0.5% BSA, pH 7.4) to a concentration of 1 µM and total volume of 250 µL. Mix fluorescent-labeled coagulation factor X (fX-fd) from step 1 at a concentration of 500 nM with the phospholi…

Materials

Alexa Fluor 647 NHS Ester (Succinimidyl Ester)	Thermo Fisher Scientific	A37573	Fluorescent dye
BD FACSCantoII	BD Bioscience
DiIC16(3) (1,1'-Dihexadecyl-3,3,3',3'-Tetramethylindocarbocyanine Perchlorate)	Thermo Fisher Scientific	D384	Fluorescent dye
DMSO	Sigma Aldrich	D8418
HEPES	Sigma Aldrich	H4034-500G
L-α-phosphatidylserine (Brain, Porcine) (sodium salt)	Avanti Polar Lipids	840032P
L-α-phosphatidylcholine (Brain, Porcine)	Avanti Polar Lipids	840053P
Mini-Extruder	Avanti Polar Lipids	610020-1EA
Potassium chloride	Sigma Aldrich	P9541-500G
Calcium chloride, anhydrous, powder, ≥97%	Sigma Aldrich	C4901-100G
Sodium phosphate monobasic	Sigma Aldrich	S3139-250G
Sodium chloride	Sigma Aldrich	S3014-500G
Magnesium chloride	Sigma Aldrich	M8266-100G
Bovine serum albumin	VWR Life Science AMRESCO	Am-O332-0.1
EDTA disodium salt	VWR Life Science AMRESCO	Am-O105B-0.1