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对KSR结合的MEK药物的作用的结构基础
Zaigham M Khan1,2, Alexander M Real1,2, William M Marsiglia1,2
1Department of Oncological Sciences, The Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Nature
|September 14, 2020
概括
新的研究揭示了MEK抑制剂如何与KSR结合,揭示了一种新的机制,通过克服耐药性,可能导致更安全,更有效的癌症疗法.
科学领域:
- 生物化学
- 分子生物学
- 药物发现
背景情况:
- 中原激活蛋白激酶 (MEK) 是瘤学,免疫疗法和衰老研究的关键目标.
- 目前的MEK抑制剂由于目标毒性和耐药性而面临限制.
- 了解MEK在生理综合体中的功能对于开发改进的疗法至关重要.
研究的目的:
- 阐明生理复合体内MEK抑制的结构基础.
- 研究与KSR复合的MEK抑制剂的结合机制.
- 为下一代MEK抑制剂的设计提供信息,以提高有效性和降低耐药性.
主要方法:
- 使用X射线结晶学来确定与KSR和各种MEK抑制剂结合的MEK结构.
- 进行了药物向相互作用和结合动力学的分析.
- 基于结构洞察力开发了一种新型抑制剂,特拉米.
主要成果:
- 在X射线晶体结构中发现了一种意想不到的结合模式,即特拉美丁尼在MEK接口上与KSR发生接触.
- KSR重塑了MEK抑制剂的囊,影响了结合和药物停留时间.
- 通过保留的接口残留物,Trametinib与KSR-MEK结合破坏了相关的RAF-MEK复合物.
结论:
- 这项研究揭示了MEK接口口的可塑性及其与KSR的相互作用.
- 这些发现为设计更安全,更有效的MEK抑制剂提供了分子模板.
- 开发的特拉米表明了限制MEK抑制的适应性抵抗的策略.
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