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在 (13)C同位素标记β片中异常的红外胺I强度分布来自延伸的多链结构:一项ab initio研究
1Department of Chemistry (M/C 111), University of Illinois at Chicago, 845 West Taylor Street, Room 4500 SES, Chicago, IL 60607-7061, USA.
Journal of the American Chemical Society
|June 21, 2001
概括
酸中的多链β片结构导致异常的红外吸收光谱强度. 在同位素标记的中观察到的这种效应,随着叶子尺寸的增加而增大,有助于进行β-叶子折叠动态研究.
科学领域:
- 计算化学是一种计算化学.
- 频谱学是一种光谱学.
- 生物物理学的生物物理.
背景情况:
- 胺I红外吸收光谱对于研究二次结构至关重要.
- 之前的研究报告了标记中的同位素转移胺I的异常强度.
研究的目的:
- 模拟以反平行β片形态对同位素替代的胺I红外吸收光谱.
- 为了阐明13C标记的异常强度的原因.
主要方法:
- 一开始计算力场和原子极张量.
- 模拟红外吸收光谱对具有不同数量的反平行β-sheet链的的模拟 (n=2-5).
主要成果:
- 标记13C的异常强度归因于多链式β片的形成.
- 胺I模式分裂和强度增强随着β片尺寸的增加而增加.
- 最强的转换涉及在更大的板的内链上标记的胺的相联模式.
结论:
- 多链式反平行β片结构解释了同位素替代中的异常红外强度.
- 这些发现提供了对标记中的IR强度机制的详细了解.
- 这种知识使得能够设计特定站点的探测器来测试β-sheet折叠动态.
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