Abe I, Okumoto K, Tamura S, Fujiki Y
Department of Biology, Faculty of Science, Kyushu University, Fukuoka, Japan.
FEBS Lett. 1998 Jul 24;431(3):468-72. doi: 10.1016/s0014-5793(98)00815-1.
We cloned a human PEX11 cDNA by expressed sequence tag homology search using yeast Candida boidinii PEX11, followed by screening of human liver cDNA library. PEX11 encoded a peroxisomal protein Pex11p comprising 247 amino acids, with two transmembrane segments and a dilysine motif at the C-terminus. Pex11p comigrated in SDS-PAGE with a 28-kDa peroxisomal integral membrane protein (PMP28) isolated from the liver of clofibrate-treated rats and was crossreactive to anti-PMP28 antibody, thereby indicating PEX11 to encode PMP28. Pex11p exposes both N- and C-terminal parts to the cytosol. PEX11 was not responsible for ten complementation groups of human peroxisome deficiency disorders.
我们利用博伊丁假丝酵母的PEX11通过表达序列标签同源性搜索克隆了人PEX11 cDNA,随后筛选人肝脏cDNA文库。PEX11编码一种过氧化物酶体蛋白Pex11p,其包含247个氨基酸,有两个跨膜区段以及位于C端的双赖氨酸基序。Pex11p在SDS-PAGE中与从经氯贝丁酯处理的大鼠肝脏中分离出的28 kDa过氧化物酶体整合膜蛋白(PMP28)迁移率相同,并且与抗PMP28抗体发生交叉反应,从而表明PEX11编码PMP28。Pex11p的N端和C端均暴露于细胞质中。PEX11与人类过氧化物酶体缺乏症的十个互补组无关。