Crepaldi Domingues Cleyton, Ciana Annarita, Buttafava Armando, Balduini Cesare, de Paula Eneida, Minetti Giampaolo
Departamento de Bioquímica, Instituto de Biologia, Universidade Estadual de Campinas, Campinas, SP, Brazil.
J Membr Biol. 2009 Jan;227(1):39-48. doi: 10.1007/s00232-008-9142-4. Epub 2008 Dec 9.
Lipid rafts are microdomains enriched in cholesterol and sphingolipids that contain specific membrane proteins. The resistance of domains to extraction by nonionic detergents at 4 degrees C is the commonly used method to characterize these structures that are operationally defined as detergent-resistant membranes (DRMs). Because the selectivity of different detergents in defining membrane rafts has been questioned, we have compared DRMs from human erythrocytes prepared with two detergents: Triton X-100 and C12E8. The DRMs obtained presented a cholesterol/protein mass ratio three times higher than in the whole membrane. Flotillin-2 was revealed in trace amounts in DRMs obtained with C12E8, but it was almost completely confined within the DRM fraction with Triton X-100. Differently, stomatin was found distributed in DRM and non-DRM fractions for both detergents. We have also measured the order parameter (S) of nitroxide spin labels inserted into DRMs by means of electron paramagnetic resonance. The 5- and 16-stearic acid spin label revealed significantly higher S values for DRMs obtained with either Triton X-100 or C12E8 in comparison to intact cells, while the difference in the S values between Triton X-100 and C12E8 DRMs was not statistically significant. Our results suggest that although the acyl chain packing is similar in DRMs prepared with either Triton X-100 or C12E8 detergent, protein content is dissimilar, with flotillin-2 being selectively enriched in Triton X-100 DRMs.
脂筏是富含胆固醇和鞘脂的微结构域,其中包含特定的膜蛋白。在4℃下用非离子去污剂提取这些结构域的抗性是表征这些结构的常用方法,这些结构在操作上被定义为抗去污剂膜(DRM)。由于不同去污剂在定义膜筏方面的选择性受到质疑,我们比较了用两种去污剂(Triton X-100和C12E8)制备的人红细胞DRM。所获得的DRM的胆固醇/蛋白质质量比是全细胞膜的三倍。在用C12E8获得的DRM中微量检测到了小窝蛋白-2,但在用Triton X-100时它几乎完全局限于DRM组分中。不同的是,两种去污剂处理后,气孔蛋白分布在DRM和非DRM组分中。我们还通过电子顺磁共振测量了插入DRM中的氮氧化物自旋标记的序参数(S)。与完整细胞相比,5-和16-硬脂酸自旋标记显示,用Triton X-100或C12E8获得的DRM的S值显著更高,而Triton X-100和C12E8 DRM之间的S值差异无统计学意义。我们的结果表明,尽管用Triton X-100或C12E8去污剂制备的DRM中酰基链堆积相似,但蛋白质含量不同,小窝蛋白-2选择性地富集在Triton X-100 DRM中。