Recent progress of methods for cuproptosis detection

IF 3.9 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Frontiers in Molecular Biosciences Pub Date : 2024-09-04 DOI:10.3389/fmolb.2024.1460987
Ligang Zhang, Ruiting Deng, Raoqing Guo, Yawen Jiang, Yichen Guan, Caiyue Chen, Wudi Zhao, Guobin Huang, Lian Liu, Hongli Du, Dongsheng Tang
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Abstract

Varying from other identified cell death pathways, cuproptosis is a new type of regulated cell death characterized by excess Cu ions, abnormal aggregation of lipoylated proteins in TCA cycle, loss of Fe-S cluster proteins, upregulation of HSP70, leading to proteotoxic and oxidative stress. Cuproptosis is highly concerned by scientific community and as the field of cuproptosis further develops, remarkable progress has been made in the verification and mechanism of cuproptosis, and methods used to detect cuproptosis have been continuously improved. According to the characteristic changes of cuproptosis, techniques based on cell death verification, Cu content, morphology, molecular biology of protein levels of cuproptosis-related molecules and biochemical pathways of cuproptosis-related enzyme activity and metabolites of oxidative stress, lipoic acid, TCA cycle, Fe-S cluster proteins, oxidative phosphorylation, cell respiration intensity have been subject to cuproptosis verification and research. In order to further deepen the understanding of detecting cuproptosis, the principle and application of common cuproptosis detection methods are reviewed and categorized in cellular phenomena and molecular mechanism in terms of cell death, Cu content, morphology, molecular biology, biochemical pathways with a flow chart. All the indicating results have been displayed in response to the markers of cuproptosis, their advantages and limitations are summaried, and comparison of cuproptosis and ferroptosis detection is performed in this study. Our collection of methods for cuproptosis detection will provide a great basis for cuproptosis verification and research in the future.
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杯突检测方法的最新进展
与其他已发现的细胞死亡途径不同,杯突症是一种新型的调节性细胞死亡,其特点是Cu离子过量、脂酰化蛋白在TCA循环中异常聚集、Fe-S簇蛋白丢失、HSP70上调,从而导致蛋白毒性和氧化应激。杯突症受到科学界的高度关注,随着杯突症领域的进一步发展,人们在杯突症的验证和机制方面取得了显著的进展,用于检测杯突症的方法也在不断改进。根据杯突症的特征性变化,基于细胞死亡验证、Cu 含量、形态学、杯突症相关分子蛋白水平的分子生物学、杯突症相关酶活性的生化通路以及氧化应激、硫辛酸、TCA 循环、Fe-S 簇蛋白、氧化磷酸化、细胞呼吸强度等代谢产物的生化通路等技术已成为杯突症验证和研究的对象。为了进一步加深对杯突症检测方法的理解,本文对常用杯突症检测方法的原理和应用进行了综述,并从细胞死亡、铜含量、形态学、分子生物学、生化途径等细胞现象和分子机制方面进行了分类,以流程图的形式展示。所有显示结果都与杯突症标志物相对应,总结了它们的优势和局限性,并在本研究中对杯突症和铁突症检测进行了比较。我们收集的杯突症检测方法将为今后的杯突症验证和研究提供重要依据。
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来源期刊
Frontiers in Molecular Biosciences
Frontiers in Molecular Biosciences Biochemistry, Genetics and Molecular Biology-Biochemistry
CiteScore
7.20
自引率
4.00%
发文量
1361
审稿时长
14 weeks
期刊介绍: Much of contemporary investigation in the life sciences is devoted to the molecular-scale understanding of the relationships between genes and the environment — in particular, dynamic alterations in the levels, modifications, and interactions of cellular effectors, including proteins. Frontiers in Molecular Biosciences offers an international publication platform for basic as well as applied research; we encourage contributions spanning both established and emerging areas of biology. To this end, the journal draws from empirical disciplines such as structural biology, enzymology, biochemistry, and biophysics, capitalizing as well on the technological advancements that have enabled metabolomics and proteomics measurements in massively parallel throughput, and the development of robust and innovative computational biology strategies. We also recognize influences from medicine and technology, welcoming studies in molecular genetics, molecular diagnostics and therapeutics, and nanotechnology. Our ultimate objective is the comprehensive illustration of the molecular mechanisms regulating proteins, nucleic acids, carbohydrates, lipids, and small metabolites in organisms across all branches of life. In addition to interesting new findings, techniques, and applications, Frontiers in Molecular Biosciences will consider new testable hypotheses to inspire different perspectives and stimulate scientific dialogue. The integration of in silico, in vitro, and in vivo approaches will benefit endeavors across all domains of the life sciences.
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