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在与核蛋白进行共免疫沉淀时,需要去除非特异性结合蛋白。

Removal of nonspecific binding proteins is required in co-immunoprecipitation with nuclear proteins.

机构信息

Hunan Province Key Laboratory of Tumor Cellular & Molecular Pathology, Cancer Research Institute, Hengyang Medical School, University of South China, Hengyang, Hunan, 421001, China.

Department of pathology, The First Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, Hunan, 421001, China.

出版信息

Biotechniques. 2022 Dec;73(6):289-296. doi: 10.2144/btn-2022-0048. Epub 2022 Nov 19.

Abstract

Whether protein samples should be pretreated to remove nonspecific binding proteins in co-immunoprecipitation (CO-IP) is controversial. In this work, nonspecific binding of proteins to agarose beads was found to be greater than that to magnetic beads. The nonspecific binding was increased with the decrease of ion concentrations but reduced by Nonidet P40. Western blot indicated that p65 and β-actin were present as nonspecifically bound protein to the beads. p53 and β-actin were present in the CO-IP precipitates of nuclear proteins but pretreatment cleared the nonspecifically pulled down p53 and β-actin. These data suggest that magnetic beads are better for CO-IP, but preclearing is necessary to minimize false positive regardless of which bead is used, particularly for nuclear proteins.

摘要

在免疫共沉淀(CO-IP)中,蛋白质样品是否需要预处理以去除非特异性结合蛋白存在争议。在这项工作中,发现蛋白质与琼脂糖珠的非特异性结合大于与磁珠的非特异性结合。非特异性结合随着离子浓度的降低而增加,但被 NP-40 减少。Western blot 表明 p65 和 β-肌动蛋白作为非特异性结合蛋白存在于珠上。p53 和 β-肌动蛋白存在于核蛋白的 CO-IP 沉淀中,但预处理可清除非特异性拉下的 p53 和 β-肌动蛋白。这些数据表明,对于 CO-IP,磁珠更好,但无论使用哪种珠,预清除都是必要的,以最小化假阳性,特别是对于核蛋白。

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