TY - JOUR
T1 - Kinetics of Ca2+-Induced Fusion of Cardiolipin-Phosphatidylcholine Vesicles
T2 - Correlation between Vesicle Aggregation, Bilayer Destabilization, and Fusion
AU - Wilschut, Jan
AU - Scholma, Janny
AU - Hoekstra, Dick
AU - Nir, Shlomo
PY - 1985/8/1
Y1 - 1985/8/1
N2 - We have investigated the kinetics of Ca2+-induced aggregation and fusion of large unilamellar vesicles composed of an equimolar mixture of bovine heart cardiolipin and dioleoylphosphatidylcholine. Mixing of bilayer lipids was monitored with an assay based on resonance energy transfer (RET) and mixing of aqueous vesicle contents with the Tb/dipicolinate assay. The results obtained with either assay were analyzed in terms of a mass action kinetic model, providing separate rate constants for vesicle aggregation and for the fusion reaction proper. At different Ca2+ concentrations, either at 25 °C or at 37 °C, aggregation rate constants derived from the data obtained with the RET assay were the same as those derived from the Tb/dipicolinate data, indicating that mixing of bilayer lipids occurred only during vesicle aggregation events that resulted in mixing of aqueous contents as well. At 25 °C, identical fusion rate constants were obtained with either assay, indicating that at this temperature the probability of lipid mixing and that of aqueous contents mixing, occurring after vesicle aggregation, were the same. The fusion rate constants for the RET assay increased more steeply with increasing temperature than the fusion rate constants derived from the Tb/dipicolinate data. As a result, at 37 °C the tendency of the vesicles, after aggregation, to mix lipids was slightly higher than their tendency to mix aqueous contents. The aggregation rate constants increased steeply with Ca2+ concentrations increasing in a narrow range (9.5-11 mM), indicating that, in addition to a Ca2+-dependent charge neutralization on the vesicle surface, structural changes in the lipid bilayer are involved in the aggregation process. Since the fusion rate constants increased remarkably in parallel with the aggregation rate constants, it is concluded that the structural changes in the vesicle bilayer, that facilitate vesicle aggregation, also cause a destabilization of the bilayer and, thus, render the vesicles susceptible to fusion.
AB - We have investigated the kinetics of Ca2+-induced aggregation and fusion of large unilamellar vesicles composed of an equimolar mixture of bovine heart cardiolipin and dioleoylphosphatidylcholine. Mixing of bilayer lipids was monitored with an assay based on resonance energy transfer (RET) and mixing of aqueous vesicle contents with the Tb/dipicolinate assay. The results obtained with either assay were analyzed in terms of a mass action kinetic model, providing separate rate constants for vesicle aggregation and for the fusion reaction proper. At different Ca2+ concentrations, either at 25 °C or at 37 °C, aggregation rate constants derived from the data obtained with the RET assay were the same as those derived from the Tb/dipicolinate data, indicating that mixing of bilayer lipids occurred only during vesicle aggregation events that resulted in mixing of aqueous contents as well. At 25 °C, identical fusion rate constants were obtained with either assay, indicating that at this temperature the probability of lipid mixing and that of aqueous contents mixing, occurring after vesicle aggregation, were the same. The fusion rate constants for the RET assay increased more steeply with increasing temperature than the fusion rate constants derived from the Tb/dipicolinate data. As a result, at 37 °C the tendency of the vesicles, after aggregation, to mix lipids was slightly higher than their tendency to mix aqueous contents. The aggregation rate constants increased steeply with Ca2+ concentrations increasing in a narrow range (9.5-11 mM), indicating that, in addition to a Ca2+-dependent charge neutralization on the vesicle surface, structural changes in the lipid bilayer are involved in the aggregation process. Since the fusion rate constants increased remarkably in parallel with the aggregation rate constants, it is concluded that the structural changes in the vesicle bilayer, that facilitate vesicle aggregation, also cause a destabilization of the bilayer and, thus, render the vesicles susceptible to fusion.
UR - http://www.scopus.com/inward/record.url?scp=0021893689&partnerID=8YFLogxK
U2 - 10.1021/bi00338a023
DO - 10.1021/bi00338a023
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C2 - 4063345
AN - SCOPUS:0021893689
SN - 0006-2960
VL - 24
SP - 4630
EP - 4636
JO - Biochemistry
JF - Biochemistry
IS - 17
ER -