Niles W D, Silvius J R, Cohen F S
Department of Molecular Biophysics and Physiology, Rush Medical College, Chicago, Illinois 60612, USA.
J Gen Physiol. 1996 Mar;107(3):329-51. doi: 10.1085/jgp.107.3.329.
Membrane fusion of a phospholipid vesicle with a planar lipid bilayer is preceded by an initial prefusion stage in which a region of the vesicle membrane adheres to the planar membrane. A resonance energy transfer (RET) imaging microscope, with measured spectral transfer functions and a pair of radiometrically calibrated video cameras, was used to determine both the area of the contact region and the distances between the membranes within this zone. Large vesicles (5-20 microns diam) were labeled with the donor fluorophore coumarin-phosphatidylethanolamine (PE), while the planar membrane was labeled with the acceptor rhodamine-PE. The donor was excited with 390 nm light, and separate images of donor and acceptor emission were formed by the microscope. Distances between the membranes at each location in the image were determined from the RET rate constant (kt) computed from the acceptor:donor emission intensity ratio. In the absence of an osmotic gradient, the vesicles stably adhered to the planar membrane, and the dyes did not migrate between membranes. The region of contact was detected as an area of planar membrane, coincident with the vesicle image, over which rhodamine fluorescence was sensitized by RET. The total area of the contact region depended biphasically on the Ca2+ concentration, but the distance between the bilayers in this zone decreased with increasing [Ca2+]. The changes in area and separation were probably related to divalent cation effects on electrostatic screening and binding to charged membranes. At each [Ca2+], the intermembrane separation varied between 1 and 6 nm within each contact region, indicating membrane undulation prior to adhesion. Intermembrane separation distances < or = 2 nm were localized to discrete sites that formed in an ordered arrangement throughout the contact region. The area of the contact region occupied by these punctate attachment sites was increased at high [Ca2+]. Membrane fusion may be initiated at these sites of closest membrane apposition.
磷脂囊泡与平面脂质双层的膜融合之前会经历一个初始的预融合阶段,在此阶段囊泡膜的一个区域会附着于平面膜。使用一台具有测量光谱转移函数的共振能量转移(RET)成像显微镜以及一对经过辐射校准的摄像机,来确定接触区域的面积以及该区域内两层膜之间的距离。用供体荧光团香豆素 - 磷脂酰乙醇胺(PE)标记大囊泡(直径5 - 20微米),而用受体罗丹明 - PE标记平面膜。用390纳米的光激发供体,显微镜形成供体和受体发射的单独图像。图像中每个位置的膜间距离由根据受体与供体发射强度比计算出的RET速率常数(kt)确定。在没有渗透梯度的情况下,囊泡稳定地附着于平面膜,并且染料不会在膜之间迁移。接触区域被检测为与囊泡图像重合的平面膜区域,在该区域罗丹明荧光通过RET被敏化。接触区域的总面积对Ca2 +浓度呈双相依赖,但该区域双层膜之间的距离随[Ca²⁺]增加而减小。面积和间距的变化可能与二价阳离子对静电屏蔽以及与带电膜结合的影响有关。在每个[Ca²⁺]下,每个接触区域内的膜间间距在1至6纳米之间变化,表明在粘附之前膜有起伏。膜间间距≤2纳米的区域定位于在整个接触区域以有序排列形成的离散位点。在高[Ca²⁺]时,这些点状附着位点所占据的接触区域面积增加。膜融合可能在这些膜最紧密贴合的位点开始。