Numerical values of CF fluorescence during metabolite delivery to vesicles of various lipid types.

Data A. Numerical values of the temporal dependence of CF fluorescence in individual vesicles made of archaeal 4ME diether G1PC lipids or bacterial diester G3PE-PG-CA lipids exposed to glycine, alanine, leucine, aspartic acid, glutamine, tryptophan, glyceraldehyde, dihydroxyacetone, glycerol, deoxyribose, ribose, arabinose, urea, cytosine, uracil, phosphonate, adenine, or guanine. These data are used in Figs 2, S1 and S2. Data B. Numerical values of the mean temporal dependence of CF fluorescence in vesicles made of bacterial diester G3PE-PG-CA lipids or bacterial diester G3PE lipids exposed to urea, glycine, glycerol, phosphonate, deoxyribose, and ribose. These data are used in S4 Fig. Data C. Numerical values of the mean temporal dependence of CF fluorescence in vesicles made of archaeal 4ME diether G1PC lipids, 4ME diether G3PC lipids, diether G3PC lipids, 4ME Diester G3PC, or bacterial diester G3PE-PG-CA lipids exposed to urea, glycine, glycerol, phosphonate, deoxyribose, and ribose. These data are used in Fig 3. Data D. Numerical values of the mean temporal dependence of CF fluorescence in vesicles made of 12:0 Diether G3PC lipids, 16:0 Diether G3PC lipids, or 18:0 Diether G3PC lipids exposed to urea, glycine, glycerol, phosphonate, deoxyribose, and ribose. These data are used in S5 Fig. Data E. Numerical values of the mean temporal dependence of CF fluorescence in vesicles made of 18:0 Diether G3PC lipids or 18:1 Diether G3PC lipids exposed to urea, glycine, glycerol, phosphonate, deoxyribose, and ribose. These data are used in S6 Fig. (XLSX)