Ohgami Nobutaka, Ko Dennis C, Thomas Matthew, Scott Matthew P, Chang Catherine C Y, Chang Ta-Yuan
Department of Biochemistry, Dartmouth Medical School, Hanover, NH 03755, USA.
Proc Natl Acad Sci U S A. 2004 Aug 24;101(34):12473-8. doi: 10.1073/pnas.0405255101. Epub 2004 Aug 16.
Niemann-Pick type C (NPC) 1 protein plays important roles in moving cholesterol and other lipids out of late endosomes by means of vesicular trafficking, but it is not known whether NPC1 directly interacts with cholesterol. We performed photoaffinity labeling of intact cells expressing fluorescent protein (FP)-tagged NPC1 by using [(3)H]7,7-azocholestanol ([(3)H]AC). After immunoprecipitation, (3)H-labeled NPC1-GFP appeared as a single band. Including excess unlabeled sterol to the labeling reaction significantly diminished the labeling. Altering the NPC1 sterol-sensing domain (SSD) with loss-of-function mutations (P692S and Y635C) severely reduced the extent of labeling. To further demonstrate the specificity of labeling, we show that NPC2, a late endosomal/lysosomal protein that binds to cholesterol with high affinity, is labeled, whereas mutant NPC2 proteins inactive in binding cholesterol are not. Vamp7, an abundant late endosomal membrane protein without an SSD but with one transmembrane domain, cannot be labeled. Binding between [(3)H]AC and NPC1 does not require NPC2. Treating cells with either U-18666A, a compound that creates an NPC-like phenotype, or with bafilomycin A1, a compound that raises late endosomal pH, has no effect on labeling of NPC1-YFP, suggesting that both drugs affect processes other than NPC1 binding to cholesterol. We also developed a procedure to label the NPC1-YFP by [(3)H]AC in vitro and showed that cholesterol is more effective in protection against labeling than its analogs epicholesterol or 5-alpha-cholestan. Overall, the results demonstrate that there is direct binding between NPC1 and azocholestanol; the binding does not require NPC2 but requires a functional SSD within NPC1.
尼曼-皮克C型(NPC)1蛋白在通过囊泡运输将胆固醇和其他脂质从晚期内体中转运出来的过程中发挥着重要作用,但NPC1是否直接与胆固醇相互作用尚不清楚。我们使用[³H]7,7-偶氮胆固醇([³H]AC)对表达荧光蛋白(FP)标记的NPC1的完整细胞进行了光亲和标记。免疫沉淀后,³H标记的NPC1-GFP呈现为一条单一的条带。在标记反应中加入过量未标记的固醇会显著减少标记。用功能丧失突变(P692S和Y635C)改变NPC1固醇感应结构域(SSD)会严重降低标记程度。为了进一步证明标记的特异性,我们发现,与胆固醇具有高亲和力结合的晚期内体/溶酶体蛋白NPC2被标记,而在结合胆固醇方面无活性的突变型NPC2蛋白则未被标记。Vamp7是一种丰富的晚期内体膜蛋白,没有SSD但有一个跨膜结构域,不能被标记。[³H]AC与NPC1之间的结合不需要NPC2。用产生NPC样表型的化合物U-18666A或提高晚期内体pH值的化合物巴弗洛霉素A1处理细胞,对NPC1-YFP标记没有影响,这表明这两种药物影响的是NPC1与胆固醇结合以外的过程。我们还开发了一种在体外通过[³H]AC标记NPC1-YFP的方法,并表明胆固醇在防止标记方面比其类似物表胆固醇或5-α-胆甾烷更有效。总体而言,结果表明NPC1与偶氮胆固醇之间存在直接结合;这种结合不需要NPC2,但需要NPC1内有功能的SSD。