Dowling Paul, Trollet Capucine, Negroni Elisa, Swandulla Dieter, Ohlendieck Kay
Department of Biology, Maynooth University, National University of Ireland, W23 F2H6 Maynooth, Co. Kildare, Ireland.
Kathleen Lonsdale Institute for Human Health Research, Maynooth University, W23 F2H6 Maynooth, Co. Kildare, Ireland.
Proteomes. 2024 Jan 16;12(1):4. doi: 10.3390/proteomes12010004.
This perspective article is concerned with the question of how proteomics, which is a core technique of systems biology that is deeply embedded in the multi-omics field of modern bioresearch, can help us better understand the molecular pathogenesis of complex diseases. As an illustrative example of a monogenetic disorder that primarily affects the neuromuscular system but is characterized by a plethora of multi-system pathophysiological alterations, the muscle-wasting disease Duchenne muscular dystrophy was examined. Recent achievements in the field of dystrophinopathy research are described with special reference to the proteome-wide complexity of neuromuscular changes and body-wide alterations/adaptations. Based on a description of the current applications of top-down versus bottom-up proteomic approaches and their technical challenges, future systems biological approaches are outlined. The envisaged holistic and integromic bioanalysis would encompass the integration of diverse omics-type studies including inter- and intra-proteomics as the core disciplines for systematic protein evaluations, with sophisticated biomolecular analyses, including physiology, molecular biology, biochemistry and histochemistry. Integrated proteomic findings promise to be instrumental in improving our detailed knowledge of pathogenic mechanisms and multi-system dysfunction, widening the available biomarker signature of dystrophinopathy for improved diagnostic/prognostic procedures, and advancing the identification of novel therapeutic targets to treat Duchenne muscular dystrophy.
这篇观点文章关注的问题是,蛋白质组学作为系统生物学的核心技术,深深融入现代生物研究的多组学领域,如何能帮助我们更好地理解复杂疾病的分子发病机制。作为一种主要影响神经肌肉系统但具有大量多系统病理生理改变特征的单基因疾病的示例,对肌肉萎缩疾病杜氏肌营养不良症进行了研究。描述了肌营养不良症研究领域的最新成果,特别提及神经肌肉变化和全身改变/适应在蛋白质组层面的复杂性。在描述自上而下与自下而上蛋白质组学方法的当前应用及其技术挑战的基础上,概述了未来的系统生物学方法。设想中的整体和整合组学生物分析将包括整合各种组学类型的研究,包括作为系统蛋白质评估核心学科的蛋白质组间和蛋白质组内研究,以及复杂的生物分子分析,包括生理学、分子生物学、生物化学和组织化学。整合的蛋白质组学研究结果有望有助于提高我们对致病机制和多系统功能障碍的详细认识,拓宽肌营养不良症可用的生物标志物特征以改进诊断/预后程序,并推动识别治疗杜氏肌营养不良症的新治疗靶点。