通过菌体显示选择具有不对称分子支架的宏环作为循环单位的策略
Titia Rixt Oppewal1, Ivar D Jansen1, Johan Hekelaar1
1Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 4, Groningen 9474 AG, The Netherlands.
Journal of the American Chemical Society
|February 16, 2022
概括
研究人员开发了一种创新的两步方法,用于制造具有不对称支架的宏环 (MP). 这种高效的策略扩大了开发新疗法和化学探测器的各种化学空间.
科学领域:
- 医学化学
- 生物技术
- 类治疗药物
背景情况:
- 宏环 (MP) 对于药物发现和化学探测有价值.
- 菌体显示是选择高亲和度结合剂的常见方法,通常使用对称循环化策略.
- 自然存在的MP通常具有不对称的支架,难以合成.
研究的目的:
- 开发一种高效的两步策略,用于合成具有不对称循环单位的宏环.
- 证明这种策略与选择MP结合剂的菌体显示的兼容性.
- 扩大开发新疗法和化学探测器的化学空间.
主要方法:
- 一个两步循环化策略,涉及编程修改独特的囊残留物和N终端氨基.
- 该策略应用于与菌体外层蛋白结合的合成和线性前体.
- 使用传统的菌体显示协议进行兼容性测试,并与目标蛋白模型进行选择.
主要成果:
- 通过使用新策略,成功合成了不对称循环单位的MP.
- 从合成和菌体显示的前体进行MP合成的演示.
- 验证该策略与菌体显示的兼容性,以便从原始库中选择MP绑定器.
结论:
- 开发的头向侧链循环化策略提供了对不对称支架的宏循环的有效访问.
- 这种方法可以将非基分量用于定制的结合和药理性质.
- 该战略扩大了化学探测器和治疗方法的开发空间.
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