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临近连接分析检测用于研究两种不同细胞上的蛋白质-蛋白质相互作用。

Proximity ligation assay to study protein-protein interactions of proteins on two different cells.

机构信息

Basic Pharmaceutical Sciences, School of Pharmacy, University of Louisiana at Monroe, LA 71201, USA.

Division of Biotechnology & Molecular Medicine & Department of Pathobiological Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, USA.

出版信息

Biotechniques. 2018 Sep;65(3):149-157. doi: 10.2144/btn-2018-0049.

Abstract

Protein-protein interactions (PPI) by homo-, hetero- or oligo-merization in the cellular environment regulate cellular processes. PPI can be inhibited by antibodies, small molecules or peptides, and this inhibition has therapeutic value. A recently developed method, the proximity ligation assay (PLA), provides detection of PPI in the cellular environment. However, most applications using this assay are for proteins expressed in the same cell. We employ PLA for the first time to study PPI of cell surface proteins on two different cells. Inhibition of PPI using a peptide inhibitor is also quantified using this assay; PLA is used to detect PPI of CD2 and CD58 between Jurkat cells (T cells) and human fibroblast-like synoviocyte-rheumatoid arthritis cells that are important in the immune response in the autoimmune disease rheumatoid arthritis. This assay provides direct evidence of inhibition of PPI of two proteins on different cell surfaces.

摘要

蛋白质-蛋白质相互作用(PPI)通过同种、异种或寡聚化在细胞环境中调节细胞过程。PPI 可以被抗体、小分子或肽抑制,这种抑制具有治疗价值。最近开发的方法,接近连接测定(PLA),提供了在细胞环境中检测 PPI 的方法。然而,大多数使用该测定的应用都是针对同一细胞中表达的蛋白质。我们首次将 PLA 用于研究两种不同细胞上的细胞表面蛋白的 PPI。使用肽抑制剂抑制 PPI 也使用该测定进行定量;PLA 用于检测 Jurkat 细胞(T 细胞)和人成纤维样滑膜细胞-类风湿关节炎细胞之间 CD2 和 CD58 之间的 PPI,这些细胞在自身免疫性疾病类风湿关节炎中的免疫反应中很重要。该测定提供了两种不同细胞表面上两种蛋白质 PPI 抑制的直接证据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38f1/6770473/92256f359fcc/btn-65-149-g1.jpg

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