Suppr超能文献

多微生物合成抑制剂 1,2-双(2-苯并咪唑基)-1,2-乙二醇与血清白蛋白的相互作用:光谱和计算研究。

Interaction of multimicrobial synthetic inhibitor 1,2-bis(2-benzimidazolyl)-1,2-ethanediol with serum albumin: spectroscopic and computational studies.

机构信息

UM-DAE Centre for Excellence in Basic Sciences, University of Mumbai, Kalina Campus, Mumbai, India.

出版信息

PLoS One. 2013;8(1):e53499. doi: 10.1371/journal.pone.0053499. Epub 2013 Jan 4.

Abstract

The molecule, 1,2-Bis(2-benzimidazolyl)-1,2-ethanediol (BBE) is known to act as a selective inhibitor of poliovirus, rhinovirus, Candida albicans, several bacterial species, and is easily synthesized by Phillips reaction. The interaction of BBE with BSA and the effects of its binding on the conformation and unfolding/refolding pathways of the protein were investigated using multispectroscopic techniques and molecular modeling. The binding studies indicate that BSA has one high affinity BBE binding site with association constant 6.02±0.05×10(4) M(-1) at 298 K. By measuring binding at different temperatures, we determined the changes in enthalpy (ΔH = -15.13±2.15 kJ mol(-1)), entropy (ΔS = 40.87±7.25 J mol(-1) K(-1)) and free energy (ΔG( = )26.78±1.02) of interaction, which indicate that the binding was spontaneous and both enthalpically and entropically driven. Based on molecular modeling and thermodynamic parameters, we proposed that the complex formation involved mainly hydrophilic interaction such as hydrogen bonding between hydroxyl groups of ethane-1,2-diol fragment with Tyr410 and benzimidazole sp(2) nitrogen atom with Ser488 and hydrophobic interaction between phenyl ring of one benzimidazole of the ligand and hydrophobic residues namely, Ile387, Cys391, Phe402, Val432 and Cys437. The sequential unfolding mechanism of BSA, site-specific marker displacement experiments and molecular modeling showed that the molecule preferably binds in subdomain IIIA. The BBE binding to BSA was found to cause both secondary and tertiary structural alterations in the protein as studied by intrinsic fluorescence, near-UV and far-UV circular dichroism results. The unfolding/refolding study showed that BBE stabilized native to intermediate states (N⇌I) transition of the protein by ∼2 kJ mol(-1) without affecting the intermediate to unfolded states (I⇌U) transition and general mechanism of unfolding of BSA.

摘要

分子 1,2-双(2-苯并咪唑基)-1,2-乙二醇(BBE)已知是脊髓灰质炎病毒、鼻病毒、白色念珠菌、几种细菌的选择性抑制剂,并且很容易通过菲利普斯反应合成。使用多光谱技术和分子建模研究了 BBE 与 BSA 的相互作用及其对蛋白质构象和展开/重折叠途径的影响。结合研究表明,BSA 具有一个高亲和力的 BBE 结合位点,在 298 K 时结合常数为 6.02±0.05×10(4) M(-1)。通过在不同温度下测量结合,我们确定了焓变(ΔH =-15.13±2.15 kJ mol(-1))、熵变(ΔS = 40.87±7.25 J mol(-1) K(-1))和自由能变(ΔG(=-26.78±1.02)),表明结合是自发的,并且焓变和熵变都是驱动力。基于分子建模和热力学参数,我们提出复合物的形成主要涉及亲水相互作用,例如乙烷-1,2-二醇片段的羟基与 Tyr410 和苯并咪唑 sp(2)氮原子与 Ser488 之间的氢键,以及配体的一个苯并咪唑的芳环与疏水残基 Ile387、Cys391、Phe402、Val432 和 Cys437 之间的疏水相互作用。BSA 的顺序展开机制、位点特异性标记位移实验和分子建模表明,该分子优先在亚结构域 IIIA 中结合。通过内源荧光、近紫外和远紫外圆二色性结果研究表明,BBE 结合 BSA 会导致蛋白质的二级和三级结构发生变化。展开/重折叠研究表明,BBE 稳定了蛋白质的天然到中间状态(N⇌I)的转变,约为 2 kJ mol(-1),而不影响中间到展开状态(I⇌U)的转变和 BSA 的一般展开机制。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验