自组装的2D阵列与de Novo蛋白质构建块
Zibo Chen, Matthew C Johnson, Jiajun Chen1
1Physical Sciences Division , Pacific Northwest National Laboratory , Richland , Washington 99352 , United States.
Journal of the American Chemical Society
|May 4, 2019
概括
科学家们设计了可编程二维自组合的新蛋白质构建块. 这一突破使得精确的蛋白质阵列构造能够克服当前生物分子工程的局限性.
科学领域:
- 蛋白质工程和结构生物学
- 生物分子自组和纳米技术
背景情况:
- 模块化DNA自组成二维数组已经很成熟.
- 实现与蛋白质相似的模块化和特异性是具有挑战性的.
- 缺少类似于DNA基配对的蛋白质特异性结合机制限制了可编程的蛋白质组合.
研究的目的:
- 开发一种使用新设计的构件设计二维蛋白质阵列的一般方法.
- 克服可编程自组的蛋白质特异性的局限性.
- 创建能够形成有序二维网格的蛋白质构建块.
主要方法:
- 设计的伪对称蛋白质构建块从一个同位体螺旋捆.
- 使用Rosetta软件进行表面重新设计,以促进自组装到C12层对称组.
- 使用负色电子显微镜和原子力显微镜验证了组装和格子几何.
主要成果:
- 十个设计的蛋白质阵列中有两个成功组装到微米尺度.
- 在组装的蛋白质阵列中观察设计的格子几何.
- 实现了高达100nm的组装尺寸,证明了受控的蛋白质自组装.
结论:
- 使用伪对称构建块设计2D蛋白质阵列的可行策略.
- 这种方法代表了可编程蛋白质自组合的重大进展.
- 正角结合接口的伪对称模式提供了精确控制蛋白质组装的途径.
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