Laboratory of Molecular Physical Chemistry , Ecole Polytechnique Fédérale de Lausanne , Station 6 , CH-1015 Lausanne , Switzerland.
Laboratory of Computational Chemistry and Biochemistry , Ecole Polytechnique Fédérale de Lausanne , CH-1015 Lausanne , Switzerland.
J Am Chem Soc. 2018 Jun 20;140(24):7554-7560. doi: 10.1021/jacs.8b02118. Epub 2018 Apr 16.
The amino acid serine has long been known to form a protonated "magic-number" cluster containing eight monomer units that shows an unusually high abundance in mass spectra and has a remarkable homochiral preference. Despite many experimental and theoretical studies, there is no consensus on a SerH structure that is in agreement with all experimental observations. Here, we present the structure of SerH determined by a combination of infrared spectroscopy and ab initio molecular dynamics simulations. The three-dimensional structure that we determine is ∼25 kcal mol more stable than the previous most stable published structure and explains both the homochiral preference and the experimentally observed facile replacement of two serine units.
丝氨酸长期以来一直被认为能够形成一个质子化的“魔术数”簇,其中包含八个单体单元,其在质谱中表现出异常高的丰度,并且具有显著的手性偏好。尽管进行了许多实验和理论研究,但对于与所有实验观察结果一致的 SerH 结构仍然没有共识。在这里,我们通过红外光谱和从头算分子动力学模拟的组合来呈现 SerH 的结构。我们确定的三维结构比以前发表的最稳定结构稳定约 25 kcal/mol,并且解释了手性偏好和实验观察到的两个丝氨酸单元的易替换性。