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源自小鼠L细胞的吞噬体膜的蛋白质和糖蛋白成分。

Protein and glycoprotein components of phagosome membranes derived from mouse L cells.

作者信息

Nagpal M L, Brown J C

出版信息

Int J Biochem. 1980;11(2):127-38. doi: 10.1016/0020-711x(80)90245-1.

DOI:10.1016/0020-711x(80)90245-1
PMID:7358196
Abstract
  1. Sodium dodecylsulfate--polyacrylamide gel electrophoresis has been employed to analyze the protein and glycorprotein components of phagosome membranes prepared from mouse L cells by the polystyrene latex bead method. 2. These experiments showed that phagosome membranes contain at least 20 major membrane protein species having apparent molecular weights between 27,000 and 250,000; the most abundant proteins have molecular weights of 112,000, 103,000, 76,000, 68,000, 62,000, 42,000 and 36,000. 3. Phagosome membrane glycoproteins, which were detected on the gels by staining with periodic acid-Schiff's reagent, were found to migrate in two broad zones centered at positions on the gel corresponding to proteins of mol. wt 140,000 and 85,000. 4. Comparison of the phagosome membrane results with the results of similar experiments carried out with cell surface membranes revealed a high degree of similarity between the two. All major protein and glycoprotein components present in phagosome membranes could be identified in both of two types of cell surface membrane preparations analyzed. 5. These results strongly support the view that phagosome membranes contain a representative, not a highly selected, sample of surface membrane proteins and glycoproteins.
摘要
  1. 已采用十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳法来分析通过聚苯乙烯乳胶珠法从小鼠L细胞制备的吞噬体膜的蛋白质和糖蛋白成分。2. 这些实验表明,吞噬体膜含有至少20种主要的膜蛋白种类,其表观分子量在27,000至250,000之间;最丰富的蛋白质分子量为112,000、103,000、76,000、68,000、62,000、42,000和36,000。3. 通过用高碘酸 - 席夫试剂染色在凝胶上检测到的吞噬体膜糖蛋白,发现在凝胶上对应于分子量为140,000和85,000的蛋白质的位置为中心的两个宽区域中迁移。4. 将吞噬体膜的结果与用细胞表面膜进行的类似实验的结果进行比较,发现两者之间有高度的相似性。在分析的两种类型的细胞表面膜制剂中都可以鉴定出吞噬体膜中存在的所有主要蛋白质和糖蛋白成分。5. 这些结果有力地支持了这样一种观点,即吞噬体膜含有表面膜蛋白和糖蛋白的代表性样本,而不是高度选择的样本。

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In vitro reassembly of vesicular stomatitis virus skeletons.水泡性口炎病毒骨架的体外重装配
J Virol. 1982 Mar;41(3):1055-62. doi: 10.1128/JVI.41.3.1055-1062.1982.
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