胰岛素聚合的结构,运动和热力学方面
Chinmaya Panda1, Sachin Kumar2, Sharad Gupta3
1Bio-interface & Environmental Engineering Lab Department of Biosciences and Bioengineering, Indian Institute of Technology Guwahati, Assam, 781039, India. lalitpandey@iitg.ac.in.
Physical chemistry chemical physics : PCCP
|September 7, 2023
概括
蛋白质聚合在疾病和药物开发中至关重要,通过动力学和热力学模型来探索. 本综述重点关注胰岛素纤维化,详细介绍途径和数学模型,以防止聚合并确保稳定的糖尿病治疗.
科学领域:
- 生物化学和制药科学 生物化学和制药科学
- 蛋白质聚合动力学和热力学.
背景情况:
- 蛋白质聚合在蛋白质病变和治疗性蛋白质开发中具有重要意义.
- 胰岛素对于糖尿病管理至关重要,由于在各种物理化学压力下聚集而面临挑战.
- 了解聚合动力学对于保持产品质量,功效和有效性至关重要.
研究的目的:
- 审查蛋白质错折和聚合的途径,数学运动模型和热力学.
- 具体讨论胰岛素纤维化,包括结构异质性和中间修改.
- 提出适合胰岛素纤维化动态数据的模型方程,并确定防止聚合的策略.
主要方法:
- 对蛋白质聚合途径和运动模型的现有文献的审查.
- 分析控制蛋白质误折叠和聚合的热力学原理.
- 讨论适用于胰岛素纤维化动态的数学模型.
主要成果:
- 详细描述蛋白质聚合途径和动力建模方法.
- 在胰岛素纤维化过程中探索结构变化和中间体.
- 识别各种适合分析胰岛素纤维化数据的模型方程.
结论:
- 该综述提供了有关在的滞后阶段诱导胰岛素结构变化的条件的见解.
- 它旨在激励开发策略,以抑制生物处理期间的胰岛素聚合级联.
- 预防胰岛素纤维化可确保糖尿病管理的稳定和全球可用的治疗方法.
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