通过蛋白关联网络探索受恶性疟原虫热休克反应影响的系统。

Q4 Pharmacology, Toxicology and Pharmaceutics International Journal of Computational Biology and Drug Design Pub Date : 2014-01-01 Epub Date: 2014-12-25 DOI:10.1504/IJCBDD.2014.066554
Timothy G Lilburn, Hong Cai, Jianying Gu, Zhan Zhou, Yufeng Wang
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引用次数: 5

摘要

热休克反应是生物体应对诸如温度突然变化、渗透和氧化应激以及暴露于有毒物质等物理损伤的一般机制。恶性疟原虫作为其生命周期的一部分,暴露于剧烈的温度变化中,并保持着广泛的热休克反应相关蛋白库。由于这些蛋白质在面对抗疟疾药物时也起到维持寄生虫的作用,因此更好地了解疟疾寄生虫中与热休克相关的系统将导致挫败这些系统的治疗方法,从而更有效地使用抗疟疾药物。在这里,我们使用蛋白质关联网络来扩大我们对受热休克反应影响和/或涉及热休克反应的系统的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Exploring systems affected by the heat shock response in Plasmodium falciparum via protein association networks.

The heat shock response is a general mechanism by which organisms deal with physical insults such as sudden changes in temperature, osmotic and oxidative stresses, and exposure to toxic substances. Plasmodium falciparum is exposed to drastic temperature changes as a part of its life cycle and maintains an extensive repertoire of heat shock response-related proteins. As these proteins serve to maintain the parasite in the face of anti-malarial drugs as well, better understanding of the heat shock-related systems in the malaria parasite will lead to therapeutic approaches that frustrate these systems, leading to more effective use of anti-malarials. Here we use protein association networks to broaden our understanding of the systems impacted by and/or implicated in the heat shock response.

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来源期刊
International Journal of Computational Biology and Drug Design
International Journal of Computational Biology and Drug Design Pharmacology, Toxicology and Pharmaceutics-Drug Discovery
CiteScore
1.00
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0.00%
发文量
8
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