调节等离子体诱导的液体硫醇化学

Q1 Medicine
Jan-Wilm Lackmann , Christina Klinkhammer , Christof Verlackt , Helena Jabloniwski , Friederike Kogelheide , Katharina Stapelmann , Annemie Bogaerts , Martina Havenith , Klaus-Dieter Weltmann , Kristian Wende
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引用次数: 0

摘要

冷物理等离子体目前正在工业和医学的各个领域进行研究。使用血浆进行伤口愈合的临床试验正在顺利进行。此外,对等离子体治疗癌症的研究也提供了有希望的发现。然而,等离子体与其生物靶点之间的化学相互作用仅被部分理解。等离子体产生的复杂化学混合物可以影响多种生物结构[1]。更好地了解这些反应将允许调整和调节等离子体的特定任务,例如触发伤口愈合或细胞凋亡级联反应。血浆对生物靶标的一个普遍影响是巯基的化学修饰,巯基在人体中执行各种关键功能,如细胞信号传导和蛋白质结构形成。由于硫醇参与组织中的许多调节和功能过程,因此深入了解等离子体治疗对硫醇的影响与优化等离子体的医疗应用高度相关。为了阐明这些相互作用,我们用不同的等离子体源研究了各种含硫醇的模型底物[2,3]。使用标准化的目标衬底,可以通过化学影响而不是物理特性来比较不同等离子体源的影响[4]。逐步增加的样品复杂性允许监测硫醇是如何受到等离子体处理的影响,在一个更加复杂的环境。结合实验证据和MD模拟,可以全面概述等离子体处理诱导的化学过程。这种结合的方法允许在分子水平上对修饰进行更全面的研究,并有助于理解基本的等离子体化学过程。了解从小分子到各种蛋白质的不同靶标如何受到血浆治疗的影响,有助于了解随后的细胞反应是如何被触发的,以及血浆治疗可能会产生哪些交叉反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Modulating Plasma-Induced Thiol Chemistry In Liquids

Cold physical plasmas are currently under investigation in various fields of industry and medicine. Clinical trials using plasma for wound healing are well under way. In addition, investigations of plasmas for cancer treatment offer promising findings, too. However, the chemical interactions between plasmas and their biological targets are only partly understood. The complex chemical cocktails generated by plasma can affect various biological structures [1]. A better understanding of these reactions would allow tuning and modulating plasmas for specific tasks, e.g. triggering wound healing or apoptosis cascades. One prevalent impact of plasma on biological targets is the chemical modification of thiol groups, which carry out various critical functions in the human body, such as cell signaling and protein structure formation. As thiols are involved in many regulatory and functional processes in tissues, an in-depth understanding of the impact of plasma treatment on thiols is highly relevant to optimize plasmas for medical applications.

To shed light onto these interactions, various thiol-containing model substrates were investigated with different plasma sources [2,3]. Using a normalized target substrate, the impact of the different plasma sources can be compared not by means of a physical characterization but by their chemical impact [4]. Stepwise increase of sample complexity allows monitoring how thiols are affected by plasma treatment in an ever more complex environment. The combination of experimental evidence and MD simulations permit a comprehensive overview of chemical processes induced by plasma treatment. This combined approach allows for a more throughout investigation of modifications on a molecular level and helps to understand fundamental plasma chemistry processes. Knowledge how different targets, ranging from small molecules to various proteins are affected by plasma treatment helps to understand how subsequent cellular responses can be triggered and what cross-reactions might be expected by plasma treatment.

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来源期刊
Clinical Plasma Medicine
Clinical Plasma Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
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