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神经母细胞瘤21至23千道尔顿蛋白中甲基化、异戊二烯化和GTP结合之间的关系。

Relationship among methylation, isoprenylation, and GTP binding in 21- to 23-kDa proteins of neuroblastoma.

作者信息

Haklai R, Kloog Y

机构信息

Department of Biochemistry, George S. Wise Faculty of Life Sciences, Tel-Aviv University, Israel.

出版信息

Cell Mol Neurobiol. 1991 Aug;11(4):415-33. doi: 10.1007/BF00711422.

Abstract
  1. Dimethylsulfoxide-induced differentiated neuroblastoma express high levels of membrane 21 to 23-kDa carboxyl methylated proteins. Relationships among methylation, isoprenylation, and GTP binding in these proteins were investigated. Protein carboxyl methylation, protein isoprenylation, and [alpha-32P]GTP binding were determined in the electrophoretically separated proteins of cells labeled with the methylation precursor [methyl-3H]methionine or with an isoprenoid precursor [3H]mevalonate. 2. A broad band of GTP-binding proteins, which overlaps with the methylated 21 to 23-kDa proteins, was detected in [alpha-32P]GTP blot overlay assays. This band of proteins was separated in two-dimensional gels into nine methylated proteins, of which four bound GTP. 3. The carboxyl-methylated 21 to 23-kDa proteins incorporated [3H]mevalonate metabolites with characteristics of protein isoprenylation. The label was not removed by organic solvents or destroyed by hydroxylamine. Incorporation of radioactivity from [3H]mevalonate was enhanced when endogenous levels of mevalonate were reduced by lovastatin, an inhibitor of mevalonate synthesis. Lovastatin blocked methylation of the 21 to 23-kDa proteins as well (greater than 70%). 4. Methylthioadenosine, a methylation inhibitor, inhibited methylation of these proteins (greater than 80%) but did not affect their labeling by [3H]mevalonate. The results suggest that methylation of the 21 to 23-kDa proteins depends on, and is subsequent to, isoprenylation. The sequence of events may be similar to that known in ras proteins, i.e., carboxyl methylation of a C-terminal cysteine that is isoprenylated. 5. Lovastatin reduced the level of small GTP-binding proteins in the membranes and increased GTP binding in the cytosol. Methylthioadensoine blocked methylation without affecting GTP binding. 6. Thus, isoprenylation appears to precede methylation and to be important for membrane association, while methylation is not required for GTP binding or membrane association. The role of methylation remains to be determined but might be related to specific interactions of the small GTP-binding proteins with other proteins.
摘要
  1. 二甲基亚砜诱导分化的神经母细胞瘤表达高水平的21至23 kDa羧甲基化蛋白。研究了这些蛋白中甲基化、异戊二烯化和GTP结合之间的关系。在用甲基化前体[甲基 - 3H]甲硫氨酸或类异戊二烯前体[3H]甲羟戊酸标记的细胞的电泳分离蛋白中,测定了蛋白羧甲基化、蛋白异戊二烯化和[α - 32P]GTP结合。2. 在[α - 32P]GTP印迹覆盖分析中检测到一条与甲基化的21至23 kDa蛋白重叠的GTP结合蛋白宽带。这条蛋白带在二维凝胶中被分离成9种甲基化蛋白,其中4种结合GTP。3. 羧甲基化的21至23 kDa蛋白掺入了具有蛋白异戊二烯化特征的[3H]甲羟戊酸代谢物。该标记不能被有机溶剂去除,也不会被羟胺破坏。当甲羟戊酸合成抑制剂洛伐他汀降低内源性甲羟戊酸水平时,[3H]甲羟戊酸的放射性掺入增加。洛伐他汀也阻断了21至23 kDa蛋白的甲基化(大于70%)。4. 甲基硫代腺苷,一种甲基化抑制剂,抑制了这些蛋白的甲基化(大于80%),但不影响它们被[3H]甲羟戊酸标记。结果表明,21至23 kDa蛋白的甲基化依赖于异戊二烯化且在其之后发生。事件顺序可能与ras蛋白中已知的相似,即异戊二烯化的C末端半胱氨酸的羧甲基化。5. 洛伐他汀降低了膜中小GTP结合蛋白的水平,并增加了胞质溶胶中的GTP结合。甲基硫代腺苷阻断甲基化而不影响GTP结合。6. 因此,异戊二烯化似乎先于甲基化且对膜结合很重要,而甲基化对于GTP结合或膜结合不是必需的。甲基化的作用仍有待确定,但可能与小GTP结合蛋白与其他蛋白的特异性相互作用有关。

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