左手和右手分子螺丝的自组装
Fei Xu1, I John Khan, Kenneth McGuinness
1Center for Advanced Biotechnology and Medicine, Department of Biochemistry and Molecular Biology, Robert Wood Johnson Medical School, Rutgers University , Piscataway, New Jersey 08854, United States.
Journal of the American Chemical Society
|November 29, 2013
概括
合成的多可以形成相同的手和相反的手结构. 这项研究发现,相反的原三环螺旋体相对有利地结合,通过槽脊机制形成板状组件.
科学领域:
- 生物化学 生物化学
- 材料科学 材料科学 材料科学
- 超分子化学 超分子化学
背景情况:
- 立体选择性在生物系统中至关重要,大多数过程都涉及同体的相互作用.
- 合成聚体表现出复杂的立体选择性,受分子间力量的影响,促使人们对一般治理原理进行调查.
- 一个几何模型表明,异体螺旋关系通常是最受青的.
研究的目的:
- 研究合成聚胺自组合中的立体选择性的一般规则.
- 为了测试使用原蛋白三重螺旋的几何槽模型.
- 为了确定左手和右手螺旋体的首选关联 (同体和异体).
主要方法:
- 三重螺旋稳定性的计算分析.
- 合成含有l-和d-proline的原蛋白三环螺旋体.
- 原子力显微镜 (AFM) 和X射线散射来描述组件.
主要成果:
- 计算预测了对异种特异性 (相反的) 关联的偏好.
- 混合左侧和右侧螺旋导致可溶性显著降低.
- 形成了片状的组件,厚度为1个的长度,X射线散射证实了紧密的里的包装.
结论:
- 这项研究支持几何模型对螺旋系统中受青的异体关联的预测.
- 相反的原三重螺旋体的自组合会产生有序的,类似板状的结构.
- 合成聚的立体选择性可以被控制以产生特定的超分子结构.
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