Halder Swagata, Surolia Avadhesha, Mukhopadhyay Chaitali
Department of Chemistry, University of Calcutta, 92, A. P. C. Road, Kolkata, 700 009, India.
Glycoconj J. 2015 Aug;32(6):371-84. doi: 10.1007/s10719-015-9601-y. Epub 2015 Jun 16.
Glycosylation has been recognized as one of the most prevalent and complex post-translational modifications of proteins involving numerous enzymes and substrates. Its effect on the protein conformational transitions is not clearly understood yet. In this study, we have examined the effect of glycosylation on protein stability using molecular dynamics simulation of legume lectin soybean agglutinin (SBA). Its glycosylated moiety consists of high mannose type N-linked glycan (Man9GlcNAc2). To unveil the structural perturbations during thermal unfolding of these two forms, we have studied and compared them to the experimental results. From the perspective of dynamics, our simulations revealed that the nonglycosylated monomeric form is less stable than corresponding glycosylated form at normal and elevated temperatures. Moreover, at elevated temperature thermal destabilization is more prominent in solvent exposed loops, turns and ends of distinct β sheets. SBA maintains it folded structure due to some important saltbridges, hydrogen bonds and hydrophobic interactions within the protein. The reducing terminal GlcNAc residues interact with the protein residues VAL161, PRO182 and SER225 via hydrophobic and via hydrogen bonding with ASN 9 and ASN 75. Our simulations also revealed that single glycosylation (ASN75) has no significant effect on corresponding cis peptide angle orientation. This atomistic description might have important implications for understanding the functionality and stability of Soybean agglutinin.
糖基化被认为是蛋白质最普遍和复杂的翻译后修饰之一,涉及众多酶和底物。其对蛋白质构象转变的影响尚未完全清楚。在本研究中,我们使用豆科凝集素大豆凝集素(SBA)的分子动力学模拟研究了糖基化对蛋白质稳定性的影响。其糖基化部分由高甘露糖型N-连接聚糖(Man9GlcNAc2)组成。为了揭示这两种形式在热解折叠过程中的结构扰动,我们进行了研究并将其与实验结果进行比较。从动力学角度来看,我们的模拟表明,在正常温度和升高温度下,非糖基化单体形式比相应的糖基化形式更不稳定。此外,在升高温度下,热不稳定在溶剂暴露的环、转角和不同β折叠片的末端更为突出。SBA由于蛋白质内一些重要的盐桥、氢键和疏水相互作用而维持其折叠结构。还原性末端GlcNAc残基通过疏水作用与蛋白质残基VAL161、PRO182和SER225相互作用,并通过与ASN 9和ASN 75形成氢键相互作用。我们的模拟还表明,单糖基化(ASN75)对相应的顺式肽角取向没有显著影响。这种原子水平的描述可能对理解大豆凝集素的功能和稳定性具有重要意义。