Rosiere T K, Marrs J A, Bouck G B
Department of Biological Sciences, University of Illinois, Chicago 60680.
J Cell Biol. 1990 Apr;110(4):1077-88. doi: 10.1083/jcb.110.4.1077.
The major integral plasma membrane protein (IP39) of Euglena gracilis was radiolabeled, peptide mapped, and dissected with proteases to identify cytoplasmic domains that bind and anchor proteins of the cell surface. When plasma membranes were radioiodinated and extracted with octyl glucoside, 98% of the extracted label was found in IP39 or the 68- and 110-kD oligomers of IP39. The octyl glucoside extracts were incubated with unlabeled cell surface proteins immobilized on nitrocellulose (overlays). Radiolabel from the membrane extract bound one (80 kD) of the two (80 and 86 kD) major membrane skeletal protein bands. Resolubilization of the bound label yielded a radiolabeled polypeptide identical in Mr to IP39. Intact plasma membranes were also digested with papain before or after radioiodination, thereby producing a cytoplasmically truncated IP39. The octyl glucoside extract of truncated IP39 no longer bound to the 80-kD membrane skeletal protein in the nitrocellulose overlays. EM of intact or trypsin digested plasma membranes incubated with membrane skeletal proteins under stringent conditions similar to those used in the nitrocellulose overlays revealed a partially reformed membrane skeletal layer. Little evidence of a membrane skeletal layer was found, however, when plasma membranes were predigested with papain before reassociation. A candidate 80-kD binding domain of IP39 has been tentatively identified as a peptide fragment that was present after trypsin digestion of plasma membranes, but was absent after papain digestion in two-dimensional peptide maps of IP39. Together, these data suggest that the unique peripheral membrane skeleton of Euglena binds to the plasma membrane through noncovalent interactions between the major 80-kD membrane skeletal protein and a small, papain sensitive cytoplasmic domain of IP39. Other (62, 51, and 25 kD) quantitatively minor peripheral proteins also interact with IP39 on the nitrocellulose overlays, and the possible significance of this binding is discussed.
纤细裸藻的主要整合质膜蛋白(IP39)被放射性标记、进行肽图谱分析并用蛋白酶切割,以鉴定结合并锚定细胞表面蛋白的胞质结构域。当质膜用放射性碘标记并用辛基葡糖苷提取时,98%的提取标记物存在于IP39或IP39的68-kD和110-kD寡聚体中。将辛基葡糖苷提取物与固定在硝酸纤维素上的未标记细胞表面蛋白一起孵育(覆盖法)。膜提取物中的放射性标记物与两条主要膜骨架蛋白带(80 kD和86 kD)中的一条(80 kD)结合。结合标记物的再溶解产生了一个Mr与IP39相同的放射性标记多肽。完整的质膜在放射性碘标记之前或之后也用木瓜蛋白酶消化,从而产生胞质截短的IP39。截短的IP39的辛基葡糖苷提取物不再与硝酸纤维素覆盖物中的80-kD膜骨架蛋白结合。在与膜骨架蛋白一起孵育的完整或经胰蛋白酶消化的质膜的电镜观察中,在类似于硝酸纤维素覆盖法的严格条件下,发现了部分重新形成的膜骨架层。然而,当质膜在重新结合之前先用木瓜蛋白酶预消化时,几乎没有发现膜骨架层的证据。IP39的一个候选80-kD结合结构域已初步鉴定为一个肽片段,该片段在质膜经胰蛋白酶消化后存在,但在IP39的二维肽图谱中经木瓜蛋白酶消化后不存在。这些数据共同表明,裸藻独特的外周膜骨架通过主要的80-kD膜骨架蛋白与IP39的一个小的、对木瓜蛋白酶敏感的胞质结构域之间的非共价相互作用与质膜结合。其他(62 kD、51 kD和25 kD)数量较少的外周蛋白也在硝酸纤维素覆盖物上与IP39相互作用,并讨论了这种结合的可能意义。