Nemoto T, Roi R, Matsusaka T, Iwanari H, Yamashita H, Kyakumoto S, Sato N
Department of Biochemistry, Iwate Medical University School of Dentistry, Morioka, Japan.
Biochem Mol Biol Int. 1997 Aug;42(5):881-9. doi: 10.1080/15216549700203321.
The purpose of this study was to develop monoclonal antibodies (mAbs) that distinguish between the two isoforms of human 90-kDa heat shock protein (HSP90), i.e., HSP90 alpha and beta. Human HSP90 alpha and beta isoforms expressed in Escherichia coli were separately used as antigens for developing the mAbs. Twenty-three and ten mAbs were obtained by immunization of mice with HSP90 alpha and beta, respectively. Among them, ten and three mAbs specifically recognized HSP90 alpha and beta isoforms, respectively, on the criteria of both enzyme-linked immunosorbent and immunoblotting analyses. Immunochemical analysis by use of the mAbs revealed that both of the HSP90 isoforms were present in human cells even under unstressed conditions and that the expression of HSP90 alpha was more strongly induced when the cells were exposed to arsenate. This is the first report of the development of the mAbs discriminating between the two isoforms of HSP90. The mAbs specific for HSP90 isoforms should be useful for the regulational and functional analyses of HSP90 isoforms.
本研究的目的是开发能够区分人90 kDa热休克蛋白(HSP90)的两种亚型,即HSP90α和β的单克隆抗体(mAb)。在大肠杆菌中表达的人HSP90α和β亚型分别用作开发mAb的抗原。通过用HSP90α和β免疫小鼠,分别获得了23个和10个mAb。其中,根据酶联免疫吸附和免疫印迹分析标准,分别有10个和3个mAb特异性识别HSP90α和β亚型。使用这些mAb进行的免疫化学分析表明,即使在未受应激的条件下,两种HSP90亚型也存在于人类细胞中,并且当细胞暴露于砷酸盐时,HSP90α的表达诱导更强。这是关于开发区分HSP90两种亚型的mAb的首次报道。对HSP90亚型具有特异性的mAb应该有助于对HSP90亚型进行调节和功能分析。