Fig. 2From: Genetically encoded phosphatidylserine biosensor for in vitro, ex vivo and in vivo labellingSurface plasmon resonance (SPR) revealed the specificity of C2 fusion proteins to PS in artificial hybrid bilayer lipid membranes (hBLM). a Schematic representation of SPR: the monochromatic light is reflected on a gold surface. At a certain angle, where the surface plasmons are excited, the reflected light has a minimum, which is continuously measured. The angle changes upon protein binding on the lipid surface. b–f, i Representative SPR sensorgrams of C2, C2-mKate, C2m2-mKate, C2-SNAP, C2m2-SNAP binding to the membranes of different composition: neutral hBLM composed of cholesterol and phosphatidylcholine (PC:Chol), phosphatidylethanolamine-enriched hBLM (PC:Chol:PE), phosphatidylserine-enriched hBLM (PC:Chol:PS). b–f, ii Quantification of C2 fusion protein binding after wash-out. Data are presented as means ± standard error of the mean (n = 6–8 independent measurements). Means were compared by one-way ANOVA and post-hoc Tukey test. p values < 0.05 were considered as significantBack to article page