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. 2018 Apr 25;114(8):1921–1935. doi: 10.1016/j.bpj.2018.03.014

Table 1.

Partition Coefficients of Bodipy-PC and TOE

Lipid Mixture Dye Single-Dye Fluorescence FRET (with DHE) FRET (with Bodipy-PC) Microscopy (GUVs)
DSPC/DOPC/chol Bodipy-PC 10 ± 2 11 ± 2 NA 15 ± 4
DSPC/POPC/chol Bodipy-PC 4 ± 1 NA NA
DSPC/DOPC/chol TOE 9 ± 1 9 ± 2 7 ± 1 NA
DSPC/POPC/chol TOE 5 ± 1 NA
bSM/DOPC/chol Bodipy-PC 9 ± 2 8 ± 1 NA 10 ± 2
bSM/DOPC/POPC/chol Bodipy-PC 8 ± 2 6 ± 1 NA 9 ± 2
bSM/DOPC/POPC/chol Bodipy-PC 5 ± 1 NA NA
bSM/ POPC/chol Bodipy-PC 3 ± 1 NA NA
bSM/DOPC/chol TOE 8 ± 1 10 ± 2 8 ± 1 NA
bSM/POPC/chol TOE 5 ± 1 NA

Kps of Bodipy-PC and TOE measured for different lipid mixtures, using single-dye fluorescence, FRET and fluorescence microscopy. Errors in Kp by single-dye fluorescence and FRET measurements are standard error of the free parameter calculated from nonlinear regression analysis of Eqs 3 and 4, respectively. Errors in Kp using fluorescence microscopy correspond to the standard error of 7–10 GUV measurements. NA (not available) represents the noninvestigation of Bodipy-PC homo-FRET or the limitation in measuring Kp using a microscope. The symbol () marks the FRET profiles used in the domain size investigation.