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开发和鉴定磷酸泛素抗体,以监测细胞和组织中的 PINK1-PRKN 信号转导。

Development and characterization of phospho-ubiquitin antibodies to monitor PINK1-PRKN signaling in cells and tissue.

机构信息

Department of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.

Department of Neurology, Faculty of Medical Sciences in Katowice, Medical University of Silesia, Katowice, Poland.

出版信息

Autophagy. 2024 Sep;20(9):2076-2091. doi: 10.1080/15548627.2024.2356490. Epub 2024 May 27.

Abstract

The selective removal of dysfunctional mitochondria, a process termed mitophagy, is critical for cellular health and impairments have been linked to aging, Parkinson disease, and other neurodegenerative conditions. A central mitophagy pathway is orchestrated by the ubiquitin (Ub) kinase PINK1 together with the E3 Ub ligase PRKN/Parkin. The decoration of damaged mitochondrial domains with phosphorylated Ub (p-S65-Ub) mediates their elimination though the autophagy system. As such p-S65-Ub has emerged as a highly specific and quantitative marker of mitochondrial damage with significant disease relevance. Existing p-S65-Ub antibodies have been successfully employed as research tools in a range of applications including western blot, immunocytochemistry, immunohistochemistry, and enzyme-linked immunosorbent assay. However, physiological levels of p-S65-Ub in the absence of exogenous stress are very low, therefore difficult to detect and require reliable and ultrasensitive methods. Here we generated and characterized a collection of novel recombinant, rabbit monoclonal p-S65-Ub antibodies with high specificity and affinity in certain applications that allow the field to better understand the molecular mechanisms and disease relevance of PINK1-PRKN signaling. These antibodies may also serve as novel diagnostic or prognostic tools to monitor mitochondrial damage in various clinical and pathological specimens.: AD: Alzheimer disease; CCCP: carbonyl cyanide 3-chlorophenylhydrazone; ELISA: enzyme-linked immunosorbent assay; HEK293E cell: human embryonic kidney E cell; ICC: immunocytochemistry; IHC: immunohistochemistry: KO: knockout; LoB: limit of blank; LoD: limit of detection; LoQ: limit of quantification; MEF: mouse embryonic fibroblast; MSD: Meso Scale Discovery; n.s.: non-significant; nonTg: non-transgenic; PBMC: peripheral blood mononuclear cell; PD: Parkinson disease; p-S65-PRKN: phosphorylated PRKN at serine 65; p-S65-Ub: phosphorylated Ub at serine 65; Ub: ubiquitin; WT: wild-type.

摘要

功能失调的线粒体选择性去除,这一过程被称为线粒体自噬,对细胞健康至关重要,其损伤与衰老、帕金森病和其他神经退行性疾病有关。一个中央的线粒体自噬途径是由泛素(Ub)激酶 PINK1 与 E3 Ub 连接酶 PRKN/Parkin 共同协调的。用磷酸化 Ub(p-S65-Ub)修饰受损的线粒体域,通过自噬系统介导其消除。因此,p-S65-Ub 已成为线粒体损伤的高度特异性和定量标志物,与疾病有重要关联。现有的 p-S65-Ub 抗体已成功地作为研究工具应用于一系列应用中,包括 Western blot、免疫细胞化学、免疫组织化学和酶联免疫吸附测定。然而,在没有外源性应激的情况下,生理水平的 p-S65-Ub 非常低,因此难以检测,需要可靠和超灵敏的方法。在这里,我们生成并鉴定了一系列新型的重组兔单克隆 p-S65-Ub 抗体,它们在某些应用中具有高特异性和亲和力,使该领域能够更好地理解 PINK1-PRKN 信号转导的分子机制和疾病相关性。这些抗体也可能作为新型的诊断或预后工具,用于监测各种临床和病理标本中的线粒体损伤。: AD: 阿尔茨海默病; CCCP: 羰基氰化物 3-氯苯腙; ELISA: 酶联免疫吸附测定; HEK293E 细胞: 人胚肾 E 细胞; ICC: 免疫细胞化学; IHC: 免疫组织化学: KO: 敲除; LoB: 空白限; LoD: 检测限; LoQ: 定量限; MEF: 鼠胚胎成纤维细胞; MSD: Meso Scale Discovery; n.s.: 无显著差异; nonTg: 非转基因; PBMC: 外周血单核细胞; PD: 帕金森病; p-S65-PRKN: 丝氨酸 65 磷酸化 PRKN; p-S65-Ub: 丝氨酸 65 磷酸化 Ub; Ub: 泛素; WT: 野生型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdad/11346534/60ff93e4b9b8/KAUP_A_2356490_F0001_OC.jpg

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