高温下布法罗朊病毒蛋白结构区的分子动力学研究

Jiapu Zhang
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引用次数: 0

摘要

水牛朊病毒蛋白(BufPrP$^\text{C}$)的分子动力学(MD)研究[Zhang JP et al.(2016) J Biomol Struct, 34(4):762-777]表明,该蛋白在室温下(无论是在中性pH还是低pH环境下)具有非常稳定的结构。为了了解水牛对朊病毒疾病的易感性较低的原因,以及为什么BufPrP$^\text{C}$在室温下如此稳定,本文将延长我们的MD在室温下的运行时间,并将我们的研究扩展到更高的温度,进一步研究BufPrP$^\text{C}$结构。从盐桥的角度,我们发现了BufPrP$^\text{C}$在室温下如此稳定的一个重要原因,这可能是治疗朊病毒疾病的药物发现或药物设计的一个很好的线索。
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Molecular Dynamics Studies of the Bufallo Prion Protein Structured Region at Higher Temperatures
Molecular dynamics (MD) studies of buffalo prion protein (BufPrP$^\text{C}$) [Zhang JP et al.(2016) J Biomol Struct Dyn 34(4):762-777] showed that the structure of this protein is very stable at room temperature (whether under neutral pH or low pH environments). In order to understand the reason why buffalo is lowly susceptible to prion diseases and why BufPrP$^\text{C}$ is so stable at room temperature, this paper will prolong our MD running time at room temperature and extend our research to higher temperatures to study this BufPrP$^\text{C}$ structure furthermore. From the salt bridge point of view we found an important reason why BufPrP$^\text{C}$ is so stable at room temperature and this might be a nice clue of drug discovery or drug design for the treatment of prion diseases.
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