Cutler D F, Melancon P, Garoff H
J Cell Biol. 1986 Mar;102(3):902-10. doi: 10.1083/jcb.102.3.902.
The p62/E2 protein of Semliki Forest virus (SFV) is a typical transmembrane glycoprotein, with an amino-terminal lumenal domain, a transmembrane (hydrophobic) domain, and a carboxy-terminal cytoplasmic domain (or tail). Our hypothesis has been that the membrane-binding polypeptide region (membrane anchor) of this protein consists of both the transmembrane domain and the adjacent positively charged peptide, Arg-Ser-Lys, which is part of the cytoplasmic domain. We have investigated three anchor mutants of the p62 protein with respect to both their disposition and their stability in cell membranes. The construction of the three mutants has been described (Cutler, D.F., and H. Garoff, J. Cell Biol., 102:889-901). They are as follows: A1, changing the basic charge cluster from Arg-Ser-Lys(+2) to Gly-Ser-Glu(-1); A2, replacing an Ala in the middle of the hydrophobic stretch with a Glu; A3, changing the charge cluster from Arg-Ser-Lys(+2) to Gly-Ser-Met(0). All three mutants retain the transmembrane configuration of the wild-type p62. In a cell homogenate they have a cytoplasmic domain that is accessible to protease. In living cells an anti-peptide antibody specific for the cytoplasmic tail of p62 reacts with the tails of both wild-type and mutant p62s following its introduction into the cytoplasm. All three mutant proteins have Triton X-114 binding properties similar to the wild-type p62. However, when the membranes of cells expressing the three mutants or the wild-type p62 protein are washed with sodium carbonate, pH 11.5, three to four times as much mutant protein as wild-type p62 is released from the membranes. Thus the stability in cell membranes of the three mutant p62 proteins is significantly reduced.
塞姆利基森林病毒(SFV)的p62/E2蛋白是一种典型的跨膜糖蛋白,具有氨基末端的腔结构域、跨膜(疏水)结构域和羧基末端的细胞质结构域(或尾部)。我们的假设是,该蛋白的膜结合多肽区域(膜锚)由跨膜结构域和相邻的带正电荷肽段Arg-Ser-Lys组成,后者是细胞质结构域的一部分。我们研究了p62蛋白的三个锚定突变体在细胞膜中的定位及其稳定性。这三个突变体的构建方法已作过描述(卡特勒,D.F.,和H.加罗夫,《细胞生物学杂志》,102:889 - 901)。它们分别如下:A1,将碱性电荷簇从Arg-Ser-Lys(+2)变为Gly-Ser-Glu(-1);A2,将疏水片段中部的一个丙氨酸替换为谷氨酸;A3,将电荷簇从Arg-Ser-Lys(+2)变为Gly-Ser-Met(0)。所有三个突变体都保留了野生型p62的跨膜结构。在细胞匀浆中,它们具有可被蛋白酶作用的细胞质结构域。在活细胞中,一种对p62细胞质尾部特异的抗肽抗体在被引入细胞质后,能与野生型和突变型p62的尾部发生反应。所有三个突变蛋白都具有与野生型p62相似的Triton X - 114结合特性。然而,当用pH 11.5的碳酸钠洗涤表达这三个突变体或野生型p62蛋白的细胞的膜时,从膜上释放的突变蛋白量是野生型p62的三到四倍。因此,这三个突变p62蛋白在细胞膜中的稳定性显著降低。