Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts, USA.
Nat Chem Biol. 2011 Aug 7;7(9):639-47. doi: 10.1038/nchembio.625.
Cephalostatin 1, OSW-1, ritterazine B and schweinfurthin A are natural products that potently, and in some cases selectively, inhibit the growth of cultured human cancer cell lines. The cellular targets of these small molecules have yet to be identified. We have discovered that these molecules target oxysterol binding protein (OSBP) and its closest paralog, OSBP-related protein 4L (ORP4L)--proteins not known to be involved in cancer cell survival. OSBP and the ORPs constitute an evolutionarily conserved protein superfamily, members of which have been implicated in signal transduction, lipid transport and lipid metabolism. The functions of OSBP and the ORPs, however, remain largely enigmatic. Based on our findings, we have named the aforementioned natural products ORPphilins. Here we used ORPphilins to reveal new cellular activities of OSBP. The ORPphilins are powerful probes of OSBP and ORP4L that will be useful in uncovering their cellular functions and their roles in human diseases.
头抱菌素 1、OSW-1、里特嗪 B 和施韦因富尔辛 A 是天然产物,它们能够强有力地、在某些情况下选择性地抑制培养的人类癌细胞系的生长。这些小分子的细胞靶标尚未确定。我们发现这些分子靶向甾醇结合蛋白 (OSBP) 和其最接近的同源物,OSBP 相关蛋白 4L (ORP4L)——这些蛋白以前并不参与癌细胞存活。OSBP 和 ORPs 构成了一个进化上保守的蛋白质超家族,其成员被牵连到信号转导、脂质运输和脂质代谢中。然而,OSBP 和 ORPs 的功能仍然很大程度上是个谜。基于我们的发现,我们将上述天然产物命名为 ORPphilins。在这里,我们使用 ORPphilins 来揭示 OSBP 的新的细胞活性。ORPphilins 是 OSBP 和 ORP4L 的强大探针,将有助于揭示它们的细胞功能及其在人类疾病中的作用。