Institut de Pharmacologie Moléculaire et Cellulaire, Université de Nice Sophia-Antipolis and CNRS, 660 Route des lucioles, 06560, Valbonne, France.
Cell Mol Life Sci. 2013 Sep;70(18):3405-21. doi: 10.1007/s00018-012-1247-3. Epub 2013 Jan 3.
In cells, the levels of sterol vary greatly among organelles. This uneven distribution depends largely on non-vesicular routes of transfer, which are mediated by soluble carriers called lipid-transfer proteins (LTPs). These proteins have a domain with a hydrophobic cavity that accommodates one sterol molecule. However, a demonstration of their role in sterol transport in cells remains difficult. Numerous LTPs also contain membrane-binding elements, but it is not clear how these LTPs couple their ability to target organelles with lipid transport activity. This issue appears critical, since many sterol transporters are thought to act at contact sites between two membrane-bound compartments. Here, we emphasize that biochemical and structural studies provide precious insights into the mode of action of sterol-binding proteins. Recent studies on START, Osh/ORP and NPC proteins suggest models on how these proteins could transport sterol between organelles and, thereby, influence cellular functions.
在细胞中,甾醇的水平在各个细胞器中差异很大。这种不均匀的分布在很大程度上取决于非囊泡转移途径,这些途径由可溶性载体(称为脂质转移蛋白,LTP)介导。这些蛋白质具有一个带有疏水性腔的结构域,可容纳一个甾醇分子。然而,证明它们在细胞中甾醇运输中的作用仍然很困难。许多 LTP 还包含膜结合元件,但尚不清楚这些 LTP 如何将其靶向细胞器的能力与脂质运输活性联系起来。这个问题似乎很关键,因为许多甾醇转运蛋白被认为在两个膜结合隔室之间的接触部位起作用。在这里,我们强调生化和结构研究为甾醇结合蛋白的作用模式提供了宝贵的见解。最近对 START、Osh/ORP 和 NPC 蛋白的研究提出了这些蛋白如何在细胞器之间运输甾醇以及由此影响细胞功能的模型。