Munroe William H, Phillips Martin L, Schumaker Verne N
Department of Chemistry and Biochemistry University of California, Los Angeles, Los Angeles, CA 90095.
Department of Chemistry and Biochemistry University of California, Los Angeles, Los Angeles, CA 90095 Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA 90095.
J Lipid Res. 2015 Jun;56(6):1172-81. doi: 10.1194/jlr.M058735. Epub 2015 Apr 24.
HDL is typically isolated ultracentrifugally at 40,000 rpm or greater, however, such high centrifugal forces are responsible for altering the recovered HDL particle. We demonstrate that this damage to HDL begins at approximately 30,000 rpm and the magnitude of loss increases in a rotor speed-dependent manner. The HDL is affected by elevated ultracentrifugal fields resulting in a lower particle density due to the shedding of associated proteins. To circumvent the alteration of the recovered HDL, we utilize a KBr-containing density gradient and a lowered rotor speed of 15,000 rpm to separate the lipoproteins using a single 96 h centrifugation step. This recovers the HDL at two density ranges; the bulk of the material has a density of about 1.115 g/ml, while lessor amounts of material are recovered at >1.2 g/ml. Thus, demonstrating the isolation of intact HDL is possible utilizing lower centrifuge rotor speeds.
高密度脂蛋白(HDL)通常通过在40000转/分钟或更高转速下超速离心来分离,然而,如此高的离心力会改变回收的HDL颗粒。我们证明,对HDL的这种损伤在约30000转/分钟时开始,且损失程度以转子速度依赖的方式增加。HDL受升高的超速离心场影响,由于相关蛋白质的脱落导致颗粒密度降低。为避免回收的HDL发生改变,我们利用含溴化钾的密度梯度和15000转/分钟的较低转子速度,通过单个96小时的离心步骤来分离脂蛋白。这在两个密度范围内回收HDL;大部分物质的密度约为1.115克/毫升,而在密度>1.2克/毫升时回收的物质较少。因此,证明了利用较低的离心机转子速度分离完整的HDL是可行的。