Craig I F, Via D P, Sherrill B C, Sklar L A, Mantulin W W, Gotto A M, Smith L C
J Biol Chem. 1982 Jan 10;257(1):330-5.
Cholesteryl ester transfer to low density lipoproteins (LDL) was achieved either by incubation of a cholesteryl ester-rich lipid microemulsion with whole plasma or by incubation of the cholesteryl ester-rich microemulsion with lipoprotein-free plasma and LDL. Sequential ultracentrifugal isolation gave LDL that contained between 5 and 37% of the cholesteryl ester derived from the artificial cholesteryl ester donor. The labeling was essentially complete within 2 h of incubation. Resonance energy transfer of LDL, labeled with fluorescent cholesteryl esters and with the surface probe 5-(N-hexadecanoylamino) fluorescein, indicated that the added cholesteryl ester was located in the inner core of the lipoprotein. In addition, biological screening of the labeled LDL in cultured cells in vitro and in the rat in vivo showed that this labeling procedure had no detectable deleterious effect on LDL. This method of labeling lipoproteins allows a rapid and specific introduction of cholesteryl esters into lipoproteins.
通过将富含胆固醇酯的脂质微乳液与全血浆一起孵育,或通过将富含胆固醇酯的微乳液与无脂蛋白血浆和低密度脂蛋白(LDL)一起孵育,可实现胆固醇酯向LDL的转移。连续超速离心分离得到的LDL含有5%至37%来自由人工胆固醇酯供体提供的胆固醇酯。孵育2小时内标记基本完成。用荧光胆固醇酯和表面探针5-(N-十六烷酰氨基)荧光素标记的LDL的共振能量转移表明,添加的胆固醇酯位于脂蛋白的内核中。此外,在体外培养细胞和体内大鼠中对标记的LDL进行生物学筛选表明,这种标记方法对LDL没有可检测到的有害影响。这种标记脂蛋白的方法允许将胆固醇酯快速、特异性地引入脂蛋白中。