Kinetics of phospholipid membrane fusion induced by surfactant apoproteins A and B

被引:56
作者
Poulain, FR
Nir, S
Hawgood, S
机构
[1] UNIV CALIF SAN FRANCISCO,DEPT PEDIAT,SAN FRANCISCO,CA 94143
[2] HEBREW UNIV JERUSALEM,FAC AGR,SEAGRAM CTR SOIL & WATER SCI,IL-76100 REHOVOT,ISRAEL
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 1996年 / 1278卷 / 02期
关键词
surfactant; surfactant apoprotein; membrane fusion; kinetics; tubular myelin; myelin;
D O I
10.1016/0005-2736(95)00212-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Surfactant apoproteins A (SP-A) and B (SP-B) interact with the lipids of surfactant and such protein-lipid interactions may be of importance in several of the steps in the surfactant cycle. We analyzed the kinetics of fusion of dipalmitoylphosphatidylcholine-phosphatidylglycerol (DPPC:PG; 7:3, w/w) phospholipid vesicles induced by SP-B alone, in the presence of 5 mM calcium, and in the presence of calcium and SP-A. Membrane fusion was measured by the method of resonance energy transfer between non-exchangeable fluorophores incorporated in the membrane, Data were analyzed using a mass action kinetic model for membrane fusion between phospholipid vesicles. We found a SP-B dose-dependent increase in lipid mixing within a range of phospholipid concentration of 5 to 100 mu M. Calcium caused a small additive increase in lipid mixing, but calcium and SP-A combined markedly increased lipid mixing induced by SP-B. Both aggregation and fusion rate constants increased with an increase in the SP-B/lipid ratio. In the presence of calcium and SP-A, the number of vesicles per fusion product markedly increased, as did the aggregation rate constants, whereas the fusion rate constants remained essentially unchanged.
引用
收藏
页码:169 / 175
页数:7
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