Schütz G J, Kada G, Pastushenko V P, Schindler H
Institute for Biophysics, University of Linz, A-4040 Linz, Austria.
EMBO J. 2000 Mar 1;19(5):892-901. doi: 10.1093/emboj/19.5.892.
The lateral motion of single fluorescence labeled lipid molecules was imaged in native cell membranes on a millisecond time scale and with positional accuracy of approximately 50 nm, using 'single dye tracing'. This first application of single molecule microscopy to living cells rendered possible the direct observation of lipid-specific membrane domains. These domains were sensed by a lipid probe with saturated acyl chains as small areas in a liquid-ordered phase: the probe showed confined but fast diffusion, with high partitioning (approximately 100-fold) and long residence time (approximately 13 s). The analogous probe with mono-unsaturated chains diffused predominantly unconfined within the membrane. With approximately 15 saturated probes per domain, the locations, sizes, shapes and motions of individual domains became clearly visible. Domains had a size of 0.7 micrometer (0.2-2 micrometer), covering approximately 13% of total membrane area. Both the liquid-ordered phase characteristics and the sizes of domains match properties of membrane fractions described as detergent-resistant membranes (DRMs), strongly suggesting that the domains seen are the in vivo correlate of DRMs and thus may be identified as lipid rafts.
利用“单染料追踪”技术,在毫秒时间尺度上对天然细胞膜中单个荧光标记脂质分子的横向运动进行成像,位置精度约为50纳米。单分子显微镜在活细胞中的首次应用使得直接观察脂质特异性膜结构域成为可能。这些结构域被具有饱和酰基链的脂质探针感知为液相有序相中的小区域:该探针显示出受限但快速的扩散,具有高分配率(约100倍)和长停留时间(约13秒)。具有单不饱和链的类似探针在膜内主要进行非受限扩散。每个结构域约有15个饱和探针,各个结构域的位置、大小、形状和运动变得清晰可见。结构域大小为0.7微米(0.2 - 2微米),覆盖约13%的总膜面积。液相有序相特征和结构域大小均与被描述为抗去污剂膜(DRMs)的膜组分特性相符,强烈表明所观察到的结构域是DRMs在体内的对应物,因此可能被鉴定为脂筏。