Webb Y, Zhou X, Ngo L, Cornish V, Stahl J, Erdjument-Bromage H, Tempst P, Rifkind R A, Marks P A, Breslow R, Richon V M
Department of Chemistry, Columbia University, New York, New York 10027, USA.
J Biol Chem. 1999 May 14;274(20):14280-7. doi: 10.1074/jbc.274.20.14280.
The ability of a novel class of hybrid polar compounds (HPCs) to induce differentiation and consequent cessation of proliferation of transformed cells has led to their development as potential chemotherapeutic agents in the treatment of cancer. Suberoylanilide hydroxamic acid (SAHA) is a prototype of a family of hydroxamic acid based compounds (SAHA-like HPCs) that can, at micromolar concentrations, induce a variety of transformed cell lines to differentiate. The mechanism of action of the HPCs is not entirely understood. Searching for a cellular target of the SAHA-like HPCs, we synthesized a photoaffinity labeling reagent structurally based on SAHA, and probed for SAHA-binding proteins in murine erythroleukemia (MEL) cells. Photoaffinity labeling in cell free extracts identified a 32-kDa protein (p32) that was specifically labeled by the photoaffinity reagent. Cell fractionation assays localized p32 to the P100 fraction. p32 was partially purified and identified by mass spectrometry as the 40 S ribosomal protein S3. Expression of epitope-tagged S3 in bacterial lysates followed by photoaffinity labeling confirmed its specific labeling. Identification of a cytodifferentiation agent target may shed light on the mechanism by which the SAHA-like HPCs exert their antitumor effects.
一类新型杂化极性化合物(HPCs)能够诱导转化细胞分化并使其增殖停止,这促使它们被开发为治疗癌症的潜在化疗药物。辛二酰苯胺异羟肟酸(SAHA)是一类基于异羟肟酸的化合物(SAHA样HPCs)的原型,这类化合物在微摩尔浓度下能够诱导多种转化细胞系分化。HPCs的作用机制尚未完全明确。为了寻找SAHA样HPCs的细胞靶点,我们合成了一种基于SAHA结构的光亲和标记试剂,并在小鼠红白血病(MEL)细胞中探测SAHA结合蛋白。无细胞提取物中的光亲和标记鉴定出一种32 kDa的蛋白(p32),该蛋白被光亲和试剂特异性标记。细胞分级分离试验将p32定位到P100组分。p32经过部分纯化,并通过质谱鉴定为40 S核糖体蛋白S3。在细菌裂解物中表达表位标记的S3,随后进行光亲和标记,证实了其特异性标记。鉴定细胞分化剂靶点可能有助于阐明SAHA样HPCs发挥抗肿瘤作用的机制。