Sonveaux N, Thines D, Ruysschaert J M
Laboratoire de Chimie-Physique des Macromolécules aux Interfaces, CP 206/2, Université Libre de Bruxelles, Belgium.
Res Virol. 1995 Jan-Feb;146(1):43-51. doi: 10.1016/0923-2516(96)80588-7.
HBsAg particles are highly immunogenic and have been shown to be a suitable support for the presentation of foreign epitopes. More information about the topology of the HBsAg protein is a prerequisite to any rational attempt to replace the region of this protein with foreign epitopes without modifying the assembly of the particles. This topology and, more precisely, the mode of interaction of the HBsAg protein with the lipid will depend on the lipid organization in the particle envelope. Nothing is known concerning the lipid organization of HBsAg particles. The only available information concerns their lipid composition. Phospholipase D hydrolysis of HBsAg particles was used here to determine whether the particles were surrounded with a lipid monolayer or bilayer. The lipid fluidity within the particle envelope was evaluated by fluorescence polarization measurements. The data strongly suggest that the HBsAg particle membrane is organized as a discontinuous rigid bilayer of lipids interacting with protein aggregates.
乙肝表面抗原(HBsAg)颗粒具有高度免疫原性,并且已被证明是呈递外源表位的合适载体。要合理尝试用外源表位替换该蛋白区域而不改变颗粒组装,就必须先了解更多关于HBsAg蛋白拓扑结构的信息。这种拓扑结构,更确切地说,HBsAg蛋白与脂质的相互作用模式将取决于颗粒包膜中的脂质组织。目前对于HBsAg颗粒的脂质组织一无所知。唯一可用的信息是它们的脂质组成。本文利用磷脂酶D对HBsAg颗粒进行水解,以确定颗粒是被脂质单层还是双层所包围。通过荧光偏振测量评估颗粒包膜内的脂质流动性。数据有力地表明,HBsAg颗粒膜是由与蛋白质聚集体相互作用的不连续刚性脂质双层构成。