Junker M, Creutz C E
Program in Biophysics, University of Virginia, Charlottesville 22908.
Biochemistry. 1993 Sep 28;32(38):9968-74. doi: 10.1021/bi00089a012.
Endonexin (annexin IV) is a member of the annexin family of homologous proteins that share the ability to bind to pure lipid membranes and to aggregate vesicles in a Ca(2+)-dependent fashion. Endonexin appears to preferentially interact with certain types of lipids such as phosphatidylglycerol (PG) in PG/phosphatidylcholine (PC) mixed lipid membranes. Such preferential binding should result in localization of PG lipids to membrane regions where endonexin is bound. This was tested using a PG derivative containing the fluorophore pyrene, which exhibits fluorescence sensitive to molecular collision frequency. Motional restriction of pyrene-PG upon endonexin-membrane binding was evident from decreased ratios of excimer-to-monomer (E/M) pyrene fluorescence with endonexin binding to 97% PG/3% pyrene-PG vesicles. A maximum decrease of 30% suggests a 30% decrease in the average diffusion constant of pyrene-PG molecules or a 53% decrease assuming that only outer-monolayer lipid molecules interact with endonexin. In vesicles containing 5% and 10% pyrene-PG in PC, segregation of lipids was evident from observed increases in E/M of 14.2 +/- 1.8% and 6.8 +/- 0.1%, respectively, in the presence of endonexin and either 10 mM (5% pyrene-PG) or 2 mM (10% pyrene-PG) free Ca2+. At higher concentrations of Ca2+ (> 10 mM for 5% pyrene-PG and > 2 mM for 10% pyrene-PG), smaller endonexin-dependent increases in E/M are observed as endonexin molecules at high surface densities compete for the limited pool of pyrene-PG. The nature of these interactions of endonexin with mixed lipid systems has implications for the way annexins may modulate membrane structure in cells.
内毒素(膜联蛋白IV)是膜联蛋白家族中同源蛋白的一员,该家族成员具有以Ca(2+)依赖方式结合纯脂质膜和聚集囊泡的能力。内毒素似乎优先与某些类型的脂质相互作用,如PG/磷脂酰胆碱(PC)混合脂质膜中的磷脂酰甘油(PG)。这种优先结合应导致PG脂质定位到内毒素结合的膜区域。使用含有荧光团芘的PG衍生物对此进行了测试,芘对分子碰撞频率具有荧光敏感性。随着内毒素与97%PG/3%芘-PG囊泡结合,芘-PG的准分子与单体(E/M)芘荧光比率降低,这表明内毒素与膜结合后芘-PG的运动受限。最大降低30%表明芘-PG分子的平均扩散常数降低30%,或者假设只有外层单分子层脂质分子与内毒素相互作用,则降低53%。在PC中含有5%和10%芘-PG的囊泡中,在存在内毒素和10 mM(5%芘-PG)或2 mM(10%芘-PG)游离Ca2+的情况下,分别观察到E/M增加14.2 +/- 1.8%和6.8 +/- 0.1%,脂质分离明显。在较高浓度的Ca2+(5%芘-PG时>10 mM,10%芘-PG时>2 mM)下,随着高表面密度的内毒素分子竞争有限的芘-PG池,观察到内毒素依赖性E/M增加较小。内毒素与混合脂质系统的这些相互作用的性质对膜联蛋白调节细胞中膜结构的方式具有重要意义。