Deepak R N V Krishna, Sankararamakrishnan Ramasubbu
Department of Biological Sciences and Bioengineering, Indian Institute of Technology Kanpur, Kanpur, India.
Department of Biological Sciences and Bioengineering, Indian Institute of Technology Kanpur, Kanpur, India.
Biophys J. 2016 May 10;110(9):1967-79. doi: 10.1016/j.bpj.2016.03.034.
Contrary to DNA double-helical structures, hydrogen bonds (H-bonds) involving nitrogen as the acceptor are not common in protein structures. We systematically searched N-H…N H-bonds in two different sets of protein structures. Data set I consists of neutron diffraction and ultrahigh-resolution x-ray structures (0.9 Å resolution or better) and the hydrogen atom positions in these structures were determined experimentally. Data set II contains structures determined using x-ray diffraction (resolution ≤ 1.8 Å) and the positions of hydrogen atoms were generated using a computational method. We identified 114 and 14,347 potential N-H…N H-bonds from these two data sets, respectively, and 56-66% of these were of the Ni+1-Hi+1…Ni type, with Ni being the proline backbone nitrogen. To further understand the nature of such unusual contacts, we performed quantum chemical calculations on the model compound N-acetyl-L-proline-N-methylamide (Ace-Pro-NMe) with coordinates taken from the experimentally determined structures. A potential energy profile generated by varying the ψ dihedral angle in Ace-Pro-NMe indicates that the conformation with the N-H…N H-bond is the most stable. An analysis of H-bond-forming proline residues reveals that more than 30% of the proline carbonyl groups are also involved in n → π(∗) interactions with the carbonyl carbon of the preceding residue. Natural bond orbital analyses demonstrate that the strength of N-H…N H-bonds is less than half of that observed for a conventional H-bond. This study clearly establishes the H-bonding capability of proline nitrogen and its prevalence in protein structures. We found many proteins with multiple instances of H-bond-forming prolines. With more than 15% of all proline residues participating in N-H…N H-bonds, we suggest a new, to our knowledge, structural role for proline in providing stability to loops and capping regions of secondary structures in proteins.
与DNA双螺旋结构不同,以氮作为受体的氢键(H键)在蛋白质结构中并不常见。我们系统地在两组不同的蛋白质结构中搜索了N-H…N H键。数据集I由中子衍射和超高分辨率X射线结构(分辨率为0.9 Å或更高)组成,这些结构中的氢原子位置是通过实验确定的。数据集II包含使用X射线衍射确定的结构(分辨率≤1.8 Å),氢原子的位置是使用计算方法生成的。我们分别从这两个数据集中鉴定出114个和14347个潜在的N-H…N H键,其中56-66%是Ni+1-Hi+1…Ni类型,Ni是脯氨酸主链氮。为了进一步了解这种异常接触的性质,我们对模型化合物N-乙酰-L-脯氨酸-N-甲基酰胺(Ace-Pro-NMe)进行了量子化学计算,其坐标取自实验确定的结构。通过改变Ace-Pro-NMe中的ψ二面角生成的势能剖面图表明,具有N-H…N H键的构象是最稳定的。对形成H键的脯氨酸残基的分析表明,超过30%的脯氨酸羰基也参与了与前一个残基的羰基碳的n→π(∗)相互作用。自然键轨道分析表明,N-H…N H键的强度不到传统H键的一半。这项研究清楚地证实了脯氨酸氮的H键形成能力及其在蛋白质结构中的普遍性。我们发现许多蛋白质中有多个形成H键的脯氨酸实例。由于所有脯氨酸残基中有超过15%参与了N-H…N H键,我们提出,据我们所知,脯氨酸在为蛋白质二级结构的环和封端区域提供稳定性方面具有一种新的结构作用。