Wang C T, Saito A, Fleischer S
J Biol Chem. 1979 Sep 25;254(18):9209-19.
We have previously described the reconstitution of functional membrane vesicles with lipid content similar to that of the normal sarcoplasmic reticulum membrane (approximately 1.0 mumol of phospholipid/mg of protein). The present study describes methodology to prepare reconstituted membrane vesicles with defined phospholipid to protein ratio, both lower and higher than that of the original membrane. The Ca2+ loading rate and efficiency are greatest in the membranes of highest protein content (0.38 mumol of phospholipid/mg of protein), decline slowly as the lipid content is quadrupled, and decrease markedly as the lipid content is quadrupled again. Such membranes of defined composition can be used to study lipid-protein interaction and to correlate membrane structure with composition. The number of particles observed by freeze-fracture electron microscopy can be correlated with protein content, whereas the percentage of smooth domain is proportional to the lipid content of the reconstituted membrane. Since 90% or more of the protein of the reconstituted membrane is the calcium pump protein, the number of particles observed by freeze-fracture is directly proportional to the amount of calcium pump protein in the membrane. The number of pump molecules calculated to be in the membrane is greater by a factor of two than the number of particles which we observed. This multiplicity ratio could be greater depending upon the assumptions made regarding the width of the membrane (see "Appendix"). Thus, it would appear that the particles consist of two or more molecules of pump protein. The change in protein concentration of the membrane is reflected also in thin sections and by negative staining. In thin sections, the broad inner and outer 70 A bands become discontinuous and patchy and, in the limit, approach a symmetrical 20,20,20 A trilayer as the protein content of the membrane becomes small. In an analogous fashion, the concentration of particles at the surface of the membrane, observed by negative staining, decreases with increasing lipid concentration in the membrane. Thus, the correlation of composition with structure can be observed by each of the three methods of sample preparation for electron microscopic analysis.
我们之前曾描述过功能性膜囊泡的重构,其脂质含量与正常肌浆网膜相似(约1.0微摩尔磷脂/毫克蛋白质)。本研究描述了制备具有特定磷脂与蛋白质比例的重构膜囊泡的方法,该比例低于和高于原始膜的比例。在蛋白质含量最高的膜(0.38微摩尔磷脂/毫克蛋白质)中,Ca2+加载速率和效率最大,随着脂质含量增加四倍,其下降缓慢,而当脂质含量再次增加四倍时则显著下降。这种特定组成的膜可用于研究脂质-蛋白质相互作用,并将膜结构与组成相关联。通过冷冻断裂电子显微镜观察到颗粒数量可与蛋白质含量相关,而光滑区域的百分比与重构膜的脂质含量成正比。由于重构膜中90%或更多的蛋白质是钙泵蛋白,通过冷冻断裂观察到的颗粒数量与膜中钙泵蛋白的量直接成正比。计算得出膜中泵分子的数量比我们观察到的颗粒数量多两倍。根据对膜宽度所做的假设,这个倍数比可能更大(见“附录”)。因此,看起来颗粒由两个或更多个泵蛋白分子组成。膜中蛋白质浓度的变化在超薄切片和负染色中也有体现。在超薄切片中,宽的内、外70埃带变得不连续且呈斑块状,并且在极限情况下,随着膜中蛋白质含量变小,接近对称的20、20、20埃三层结构。以类似的方式,通过负染色观察到的膜表面颗粒浓度随着膜中脂质浓度的增加而降低。因此,通过用于电子显微镜分析的三种样品制备方法中的每一种都可以观察到组成与结构的相关性。