Krause Martin R, Wang Minghui, Mydock-McGrane Laurel, Covey Douglas F, Tejada Emmanuel, Almeida Paulo F, Regen Steven L
Department of Chemistry, Lehigh University , Bethlehem, Pennsylvania 18015, United States.
Langmuir. 2014 Oct 21;30(41):12114-8. doi: 10.1021/la503075e. Epub 2014 Oct 10.
One of the long-standing issues surrounding cholesterol (Chol) relates to its two-faced character. In particular, the consequences of its having a rough β-face and a smooth α-face on its structural influence in cell membranes has remained elusive. In this study, direct comparisons have been made between cholesterol and a "smoothened" analog, DChol (i.e., 18,19-dinorcholesterol) using model membranes and a combination of nearest-neighbor recognition, differential scanning calorimetry, fluorescence, and monolayer measurements. Taken together, these results indicate that subtle differences exist between the interaction of these two sterols with the different states of 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC). Chol has a greater condensing power than DChol, but only slightly so, i.e., on the order of a few tens of calories per mole.
围绕胆固醇(Chol)的一个长期存在的问题涉及其两面性。特别是,其粗糙的β面和光滑的α面对细胞膜结构影响的后果仍然难以捉摸。在本研究中,使用模型膜以及最近邻识别、差示扫描量热法、荧光和单层测量相结合的方法,对胆固醇和一种“平滑化”类似物DChol(即18,19-二降胆固醇)进行了直接比较。综合这些结果表明,这两种甾醇与1,2-二棕榈酰-sn-甘油-3-磷酸胆碱(DPPC)不同状态的相互作用存在细微差异。胆固醇比DChol具有更强的凝聚能力,但只是略强,即每摩尔几十卡路里的量级。