Itoh H, Tashima Y
Department of Biochemistry, Akita University, School of Medicine, Japan.
Eur J Biochem. 1990 Oct 24;193(2):429-35. doi: 10.1111/j.1432-1033.1990.tb19356.x.
Brain 90- and 100-kDa heat-shock proteins (HSP90 and HSP100) were purified and antibodies against them prepared. The two antibodies were very specific and did not cross-react with each other. In rat, immunoblotting with the anti-HSP90 antibody showed the most abundant presence of HSP90 in testis as well as brain, compared with lung, liver, spleen, kidney, cardiac muscle, ovarium and uterus. The anti-HSP90 antibody showed the presence of a new 105-kDa protein in rat testis. This novel 105-kDa protein was also detected in brain at a very low concentration but not in HeLa cells or other organs including the uterus and ovarium. The testis 105-kDa protein was purified from rat testis; although it was clearly separable from HSP90 by two-dimensional gel electrophoresis, Q-Sepharose and hydroxyapatite column chromatographies, the properties of this protein were very similar to HSP90. The similarity was higher than 60% on peptide mapping with trypsin digestion, the 105-kDa protein cross-reacted with anti-HSP90 antibody, both were bound similarly to heparin-Sepharose gel and both are located in the cytosol fraction. When the 105-kDa protein was fractionated by HPLC, a molecular mass of 195 kDa was calculated, indicating that it is composed of two identical subunits, similarly to HSP90. The 105-kDa protein did not react with the anti-HSP100 antibody. There was a slight similarity between the 105-kDa protein and HSP100 on the peptide mapping. HSP100 was present in the microsomal fraction as well as in the cytosol. It is concluded that the 105-kDa protein is a testis-specific and HSP90-related protein.
纯化了大脑中的90 kDa和100 kDa热休克蛋白(HSP90和HSP100),并制备了针对它们的抗体。这两种抗体非常特异,且不会相互交叉反应。在大鼠中,与肺、肝、脾、肾、心肌、卵巢和子宫相比,用抗HSP90抗体进行免疫印迹显示,HSP90在睾丸和大脑中的含量最为丰富。抗HSP90抗体显示大鼠睾丸中存在一种新的105 kDa蛋白。这种新的105 kDa蛋白在大脑中也有极低浓度的存在,但在HeLa细胞或包括子宫和卵巢在内的其他器官中未检测到。从大鼠睾丸中纯化出睾丸105 kDa蛋白;尽管通过二维凝胶电泳、Q-琼脂糖凝胶和羟基磷灰石柱色谱法可将其与HSP90清晰分离,但该蛋白的特性与HSP90非常相似。用胰蛋白酶消化进行肽图分析时,相似性高于60%,105 kDa蛋白与抗HSP90抗体发生交叉反应,二者与肝素-琼脂糖凝胶的结合方式相似,且都位于胞质溶胶部分。当用高效液相色谱法分离105 kDa蛋白时,计算出其分子量为195 kDa,表明它与HSP90一样由两个相同的亚基组成。105 kDa蛋白不与抗HSP100抗体反应。在肽图分析中,105 kDa蛋白与HSP100之间存在轻微相似性。HSP100存在于微粒体部分和胞质溶胶中。结论是,105 kDa蛋白是一种睾丸特异性且与HSP90相关的蛋白。