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使用反应性生物素衍生物和125I-链霉亲和素对膜蛋白或糖蛋白上的官能团进行选择性标记。

Selective labeling of functional groups on membrane proteins or glycoproteins using reactive biotin derivatives and 125I-streptavidin.

作者信息

Roffman E, Meromsky L, Ben-Hur H, Bayer E A, Wilchek M

出版信息

Biochem Biophys Res Commun. 1986 Apr 14;136(1):80-5. doi: 10.1016/0006-291x(86)90879-x.

Abstract

Amino groups, sulfhydryl groups or oxidation-induced aldehydes on erythrocyte membrane proteins and/or glycoproteins, were reacted with biotinyl N-hydroxysuccinimide ester (BNHS), 3-(N-maleimido-propionyl) biocytin (MPB) or biocytin hydrazide (BCHZ), respectively. The detergent-lysed biotinylated samples were subjected to SDS-polyacrylamide gel electrophoresis, and the proteins were transferred onto nitrocellulose membranes. The blot was then incubated with a solution containing 125I-streptavidin, and processed for autoradiography. The advantages of this approach over previously reported procedures for labeling the three functional groups include the following: extremely high sensitivity; short exposure times of autoradiograms and relatively low levels of radioactivity; single-step radiolabeling procedures subsequent to processing and handling of gels and no background labeling in control samples.

摘要

红细胞膜蛋白和/或糖蛋白上的氨基、巯基或氧化诱导的醛基,分别与生物素化N-羟基琥珀酰亚胺酯(BNHS)、3-(N-马来酰亚胺丙酰基)生物胞素(MPB)或生物胞素酰肼(BCHZ)反应。用去污剂裂解的生物素化样品进行SDS-聚丙烯酰胺凝胶电泳,然后将蛋白质转移到硝酸纤维素膜上。接着将印迹膜与含有125I-链霉亲和素的溶液孵育,并进行放射自显影处理。与先前报道的标记这三种官能团的方法相比,该方法的优点包括:极高的灵敏度;放射自显影片的曝光时间短且放射性水平相对较低;在凝胶处理和操作后的单步放射性标记程序,以及对照样品中无背景标记。

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