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多肽链段之间NH..O和CH..O氢键的相对强度。

Relative strengths of NH..O and CH..O hydrogen bonds between polypeptide chain segments.

作者信息

Scheiner Steve

机构信息

Department of Chemistry & Biochemistry, Utah State University, Logan, Utah 84322-0300, USA.

出版信息

J Phys Chem B. 2005 Aug 25;109(33):16132-41. doi: 10.1021/jp053416d.

Abstract

Correlated ab initio calculations are used to compare the energetics when the CH and NH groups of the model dipeptide CHONHCH2CONH2 are each allowed to form a H-bond with the proton acceptor O of a peptide group. When the dipeptide is in its C7 conformation, the NH..O H-bond energy is found to be 7.4 kcal/mol, as compared to only 2.8 kcal/mol for the CH..O interaction. On the other hand, the situation reverses, and the CH..O H-bond becomes stronger than NH..O, when the dipeptide adopts a C5 structure. This reversal is important as C5 is nearly equal in stability to C7 for the dipeptide, and is representative of the commonly observed beta-sheet structure in a protein. Immersing the dipeptide-peptide pair in a model solvent weakens both sorts of H-bonds, and in a fairly uniform manner. Consequently, the trends observed in the in vacuo situation retain their validity in either aqueous solution or the protein interior. Likewise, the desolvation penalty, suffered by removing a H-bonded complex from water and placing it in the less polar interior of a protein, is quite similar for the NH..O and CH..O bonds.

摘要

采用相关的从头算方法,比较模型二肽CHONHCH2CONH2中的CH基团和NH基团分别与肽基团的质子受体O形成氢键时的能量情况。当二肽处于C7构象时,发现NH…O氢键能量为7.4千卡/摩尔,而CH…O相互作用的能量仅为2.8千卡/摩尔。另一方面,当二肽采用C5结构时,情况相反,CH…O氢键变得比NH…O更强。这种反转很重要,因为对于二肽来说,C5的稳定性与C7几乎相等,并且代表了蛋白质中常见的β-折叠结构。将二肽-肽对浸入模型溶剂中会削弱这两种氢键,且削弱方式相当均匀。因此,在真空情况下观察到的趋势在水溶液或蛋白质内部同样有效。同样,将氢键复合物从水中移除并置于蛋白质极性较小的内部所遭受的去溶剂化惩罚,对于NH…O键和CH…O键来说非常相似。

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