Frey B M, Frey F J, Lingappa V R, Trachsel H
Department of Physiology, University of California, San Francisco.
Biochem J. 1991 Apr 1;275 ( Pt 1)(Pt 1):219-25. doi: 10.1042/bj2750219.
Lipocortin I has been presumed to be synthesized and secreted in response to glucocorticoids yet the amino acid sequence of lipocortin I reveals no signal sequence typically necessary for proteins to enter the secretory pathway. The translocation of lipocortin I across membranes was analyzed in a cell-free system and in Xenopus oocytes. Based on the published sequence, the cDNA of human lipocortin I was cloned and expressed in Escherichia coli. Lipocortin I was purified and used to raise monoclonal antibodies. To test whether lipocortin I is secreted in vitro, transcribed lipocortin mRNA was translated in a wheat germ cell-free system in the absence and presence of microsomal membranes. Prolactin mRNA was used as a control for translocation of newly synthesized protein into membrane vesicles. Prolactin, but not lipocortin I, was translocated into the membranes. To test for secretion of lipocortin I in vivo, Xenopus oocytes were co-injected with transcripts encoding lipocortin I and prolactin, with and without the signal sequence. Prolactin with the signal sequence was released into the medium. However, neither prolactin without a signal sequence nor lipocortin I was released. Carbonate extraction, using an integral transmembrane protein as control, revealed no evidence for membrane integration of lipocortin I. Thus lipocortin I is not a secreted protein.
脂皮质素I被推测是响应糖皮质激素而合成和分泌的,然而脂皮质素I的氨基酸序列并未显示出蛋白质进入分泌途径通常所需的信号序列。在无细胞系统和非洲爪蟾卵母细胞中分析了脂皮质素I跨膜的转运情况。根据已发表的序列,克隆了人脂皮质素I的cDNA并在大肠杆菌中表达。纯化脂皮质素I并用其制备单克隆抗体。为了检测脂皮质素I在体外是否分泌,在有无微粒体膜存在的情况下,在麦胚无细胞系统中翻译转录的脂皮质素mRNA。催乳素mRNA用作新合成蛋白质转运到膜泡中的对照。催乳素而非脂皮质素I转运到了膜中。为了检测脂皮质素I在体内的分泌情况,将编码脂皮质素I和催乳素的转录本与有无信号序列一起共注射到非洲爪蟾卵母细胞中。带有信号序列的催乳素释放到了培养基中。然而,没有信号序列的催乳素和脂皮质素I均未释放。以一种完整跨膜蛋白为对照进行碳酸盐提取,未发现脂皮质素I整合到膜中的证据。因此,脂皮质素I不是一种分泌蛋白。