应用凝胶电泳和质谱法鉴定神经系统肿瘤中的硝基蛋白

X. Zhan, Na Li
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引用次数: 0

摘要

蛋白酪氨酸硝化是神经系统肿瘤如胶质瘤和垂体腺瘤的重要分子事件。确定酪氨酸硝化的蛋白靶点和精确修饰位点,是解决酪氨酸硝化蛋白在神经系统肿瘤中的生物学作用,发现有效的生物标志物,深入了解分子机制,确定新的诊断策略和新的治疗靶点的必要步骤。一维/二维凝胶电泳(1DGE, 2DGE)或硝基酪氨酸亲和柱(NTAC)结合串联质谱(MS/MS)已成功应用于神经系统肿瘤中硝基蛋白的分析。本文介绍了蛋白质酪氨酸硝化的基本概念,基于凝胶电泳/免疫亲和富集和串联质谱的氮蛋白组学方法,以及神经系统肿瘤中氮蛋白的研究现状。已建立的氮蛋白质组学方法很容易转化为研究其他疾病。NO和RNS是重要的炎症介质[15];(3)神经系统肿瘤中NO、过氧化物和超氧化物的生成增加[16];(4)通过生化和免疫组化方法,神经系统肿瘤中硝基酪氨酸水平高于正常组织,仅在人类神经系统肿瘤中检测到蛋白硝基微管蛋白和蛋白硝基p53[17]。此外,氨基酸类似于3-硝基酪氨酸,由于小鼠神经母细胞瘤细胞系和大鼠胶质瘤细胞系的功能和形态损伤[18]。这些研究证明了酪氨酸蛋白硝化在神经系统肿瘤发病机制中的重要性。阐明硝基蛋白的功能,可能有助于深入揭示硝基膦硝化作用在人神经系统肿瘤中的分子机制和生物学功能。通过文献综述和SwissProt网站上的蛋白质综合注释,阐述了与神经系统肿瘤相关的硝基蛋白结构域/基序、硝基酪氨酸位点的位置和可能的信号通路。在肿瘤发生发展过程中,硝基蛋白参与了多个生物学过程:(a)肿瘤细胞的迁移和侵袭[19];(b)细胞增殖和凋亡[20];(c)化疗耐药[21];(d)信号转导[22];(e)表型去分化[23];(f)微管动态稳定[24];(g)肿瘤复发;(h)其他如免疫反应和转录后调控。此外,酪氨酸硝化是一个可逆反应[25],磷酸化基序之间存在竞争[26]的发现,使我们推测蛋白质硝化的动态过程也可能受到调控。然而,酪氨酸硝化对人类神经系统肿瘤的干预尚未发现明确的靶点。研究肿瘤相关的硝基蛋白和阐明肿瘤形成的分子机制需要很长时间。
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The Use of Gel Electrophoresis and Mass Spectrometry to Identify Nitroproteins in Nervous System Tumors
Protein tyrosine nitration is an important molecular event in nervous system tumor such as glioma and pituitary adenomas. It is the essential step to identify the protein targets and exact modified sites of tyrosine nitration for addressing the biological roles of pro - tein tyrosine nitration in nervous system tumors and discovering effective biomarkers to understand in-depth molecular mechanisms and determine new diagnosis strategy and novel therapeutic targets. One/two-dimensional gel electrophoresis (1DGE, 2DGE), or nitrotyrosine affinity column (NTAC), coupled with tandem mass spectrometry (MS/MS) have been successfully applied in the analysis of nitroproteins in nervous system tumors. This article address the basic concept of protein tyrosine nitration, nitroproteomics meth - odology based on gel electrophoresis/immunoaffinity enrichment and tandem mass spectrometry, and the current status of nitroprotein study in nervous system tumors. The established nitroproteomics approach is easily translated to study other diseases. NO and RNS are important inflammatory mediators [ 15 ]; and (3) increased production of NO, peroxinitrite and superoxide, occurs in nervous system tumors [ 16 ]; (4) higher levels of nitrotyrosine are observed in nervous system tumors than normal tissues with biochemical approaches and immunohistochemical, and only protein nitrotubulin and protein nitro-p53 have been determined in human nervous system tumors [ 17]. Furthermore, the amino acid analog 3-nitrotyrosine due to functional and morphological injury of mouse-neuroblastoma cell lines and rat-glioma cell lines [ 18 ]. These studies demonstrated the importance of protein tyrosine nitration in the pathogenesis of nervous system tumors. Illustrating the functions of nitroproteins might reveal in-depth molecular mechanisms and biological function of tyro sine nitration in human nervous system tumors. Literature-based review and comprehen sive annotation of proteins on the SwissProt website were used to expound the nitroprotein domains/motifs, location of nitrotyrosine sites and possible signaling pathways relevant to nervous system tumors. Nitroproteins took part in multiple biological processes in the devel opment of tumors as follows: (a) tumor cell migration and invasion [ 19 ]; (b) cell proliferation and apoptosis [20]; (c) chemotherapy resistance [ 21 ]; (d) signal transduction [ 22]; (e) phenotypic dedifferentiation [23]; (f) microtubule dynamic stabilization [24 ]; (g) tumor recurrence; (h) others such as immunoreaction and post-transcriptional regulation. Moreover, the discov ery of tyrosine nitration being a reversible reaction [ 25 ] and having a competition between phosphorylation motif [ 26], led us to speculate that dynamic process of protein nitration might also be regulated and controlled. However, no definite target of intervention is found for tyrosine nitration in human nervous system tumors. It takes long time to study tumor-related nitroproteins and to illustrate molecular mechanisms in tumor formation.
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The Use of Gel Electrophoresis and Mass Spectrometry to Identify Nitroproteins in Nervous System Tumors Peculiarities of SDS-PAGE of Titin/Connectin Improving Tribological Behavior of Porous Anodic Film by Electrophoretic Impregnation by a Tio2 Synthesized Nanoparticle Two-Dimensional Gel Electrophoresis as an Information Base for Human Proteome Electrophoresis in the Comet Assay
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