Podack E R, Müller-Eberhard H J, Horst H, Hoppe W
J Immunol. 1982 May;128(5):2353-7.
The three-dimensional structure of recombinants of the isolated membrane attack complex (MAC) of complement with single bilayer dioleoyllecithin (DOL) vesicles and with dimyristoyllecithin (DML) vesicles was determined. A total of four MAC-vesicle complexes were analyzed by imaging negatively stained specimens at various defined tilting angles under minimal dose conditions in the electron microscope and by computer-aided three-dimensional reconstruction. The information on electron micrographs obtained at 6 degrees angular increments from +60 degrees to -60 degrees was digitized by densitometric scanning, Fourier-transformed, corrected for imaging errors, cross-correlated, and synthesized to the three-dimensional image. All four MAC-vesicle recombinants showed stain penetration into the interior of the vesicle, indicating increased permeability of the bilayer to negative stain. The MAC appeared as a hollow structure of 16-nm height, 2.0-nm wall thickness, and a 3.0-nm torus at the free end with an outer and inner diameter of 20.0 nm and 10.0 nm. In MAC-DOL vesicles the hollow core of the MAC terminated at the membrane-binding site, and only small pores of up to 2.0-nm in diameter penetrated the bilayer. In one MAC-DML vesicle lipid discontinuities on the outer circumference of the MAC binding site mediated stain penetration. The second MAC-DML vesicle showed a channel of approximately 4.0 nm connecting the hollow core of the MAC across the bilayer with the vesicle interior. The results suggest the MAC may mediate increased membrane permeability by protein channel formation in addition to lipid reorientation.
测定了补体的分离膜攻击复合物(MAC)与单层二油酰卵磷脂(DOL)囊泡以及与二肉豆蔻酰卵磷脂(DML)囊泡重组体的三维结构。通过在电子显微镜下在最小剂量条件下以各种确定的倾斜角度对负染色标本进行成像,并通过计算机辅助三维重建,共分析了四种MAC-囊泡复合物。从+60度到-60度以6度角增量获得的电子显微照片信息通过密度扫描进行数字化处理,进行傅里叶变换,校正成像误差,互相关,并合成三维图像。所有四种MAC-囊泡重组体均显示染色剂渗透到囊泡内部,表明双层对负染色剂的通透性增加。MAC呈现为高度为16纳米、壁厚为2.0纳米、自由端有一个外径为20.0纳米、内径为10.0纳米的3.0纳米环面的中空结构。在MAC-DOL囊泡中,MAC的中空核心在膜结合位点处终止,并且只有直径最大为2.0纳米的小孔穿透双层。在一个MAC-DML囊泡中,MAC结合位点外周的脂质不连续性介导了染色剂渗透。第二个MAC-DML囊泡显示出一个约4.0纳米的通道,该通道将MAC的中空核心穿过双层与囊泡内部相连。结果表明,除了脂质重排外,MAC可能通过形成蛋白质通道来介导膜通透性的增加。