Maksaev G I, Samsonov A V, Lipatov A S, Bychenko A B, Frolov V A
Frumkin Institute of Electrochemistry, Russian Academy of Sciences, Moscow.
Membr Cell Biol. 2000;14(3):397-411.
One of the key stages of cell infection with influenza virus is the enveloped virus fusion with the cell endosome membrane. To study fusion of single fluorescently-labeled influenza virions with a model bilayer membrane (BLM), a special model system was developed. A small patch of BLM with several adsorbed virions was localized upon a contact with a glass micropipette. Low pH of solution inside the pipette triggered fusion that could be registered by a change in the conductance and integral fluorescence of the BLM patch. It has been shown that the fusion initiation is followed by an increase of fluorescence signal due to the probe redistribution from the virus membrane to the BLM fragment. The increase in fluorescence was accompanied by changes in conductance. Usually, from two to five periods of the channel activity were observed, each of which probably corresponded to fusion of a single virion. It has been found that electric activity was completely inhibited by amantadine known as a blocking agent of M2 channels. This allows one to suggest that the observed changes in conductance are connected with the activity of M2 channels in the virus membrane, whose electric accessibility was the result of fusion of single virions with BLM.
流感病毒感染细胞的关键阶段之一是包膜病毒与细胞内体膜的融合。为了研究单个荧光标记的流感病毒粒子与模型双层膜(BLM)的融合,开发了一种特殊的模型系统。当与玻璃微量移液器接触时,带有几个吸附病毒粒子的一小片BLM会被定位。移液器内溶液的低pH值引发融合,这可以通过BLM片的电导率和积分荧光的变化来记录。结果表明,由于探针从病毒膜重新分布到BLM片段,融合起始后荧光信号会增加。荧光增加伴随着电导率的变化。通常,观察到两到五个通道活动周期,每个周期可能对应于单个病毒粒子的融合。已经发现,金刚烷胺(一种已知的M2通道阻滞剂)完全抑制了电活动。这使得人们可以推测,观察到的电导率变化与病毒膜中M2通道的活性有关,其电可及性是单个病毒粒子与BLM融合的结果。