摘要
在这篇综述中,我们首先研究了由光敏剂引发的单态氧对蛋白质中氨基酸残基的化学修饰机制。单峰氧有能力对细胞蛋白质造成广泛的化学损伤。因此,它在肿瘤光动力治疗中的应用需要发展出在保留正常组织的同时对恶性细胞光敏剂进行特殊处理的方法。我们描述了实现这一目标的三个目标范例。第一种是使用对目标蛋白具有高度亲和力的光敏剂;在这种情况下,光敏剂是乙酰胆碱酯酶的亚甲蓝。第二种模式是使用疏水性光敏剂金丝桃素,它能够选择性地与部分展开形式的蛋白质相互作用,包括快速分裂或病毒感染的新生物种和癌细胞,优先作用于膜界面。在这种情况下,部分展开的乙酰胆碱酯酶熔融球物种作为模型系统。在第三种模式中,光动力方法利用“最先进”化学疗法中的一般方法,将光敏剂大黄素与特定的肽激素GnRH耦合,后者通过其表面的特定GnRH受体识别恶性细胞。
关键词: 单峰氧,光敏剂,氨基酸氧化,乙酰胆碱酯酶,癌症,药物靶向,肽激素
Current Medicinal Chemistry
Title:Generation of Reactive Oxygen Species by Photosensitizers and their Modes of Action on Proteins
Volume: 25 Issue: 40
关键词: 单峰氧,光敏剂,氨基酸氧化,乙酰胆碱酯酶,癌症,药物靶向,肽激素
摘要: In this review, we first survey the mechanisms underlying the chemical modification of amino acid residues in proteins by singlet oxygen elicited by photosensitizers. Singlet oxygen has the capacity to cause widespread chemical damage to cellular proteins. Its use in photodynamic therapy of tumors thus requires the development of methodologies for specific addressing of the photosensitizer to malignant cells while sparing normal tissue. We describe three targeting paradigms for achieving this objective. The first involves the use of a photosensitizer with a high affinity for its target protein; in this case, the photosensitizer is methylene blue for acetylcholinesterase. The second paradigm involves the use of the hydrophobic photosensitizer hypericin, which has the capacity to interact selectively with partially unfolded forms of proteins, including nascent species in rapidly dividing or virus-infected and cancer cells, acting preferentially at membrane interfaces. In this case, partially unfolded molten globule species of acetylcholinesterase serve as the model system. In the third paradigm, the photodynamic approach takes advantage of a general approach in ‘state-of-the-art’ chemotherapy, by coupling the photosensitizer emodin to a specific peptide hormone, GnRH, which recognizes malignant cells via specific GnRH receptors on their surface.
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Cite this article as:
Generation of Reactive Oxygen Species by Photosensitizers and their Modes of Action on Proteins, Current Medicinal Chemistry 2018; 25 (40) . https://dx.doi.org/10.2174/0929867325666180104153848
DOI https://dx.doi.org/10.2174/0929867325666180104153848 |
Print ISSN 0929-8673 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-533X |
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