氨基酸基分子胶束的分子模拟表征。

Open journal of physical chemistry Pub Date : 2019-11-01 Epub Date: 2019-11-29 DOI:10.4236/ojpc.2019.94014
Alexander Billiot, Yayin Fang, Kevin F Morris
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引用次数: 2

摘要

手性药物的对映体通常具有不同的效力、毒性和生化特性。因此,FDA和其他全球监管机构要求制造商测试和证明手性药物的对映体纯度。自20世纪90年代以来,氨基酸基分子胶束(AABMM)被用于手性CE分离,因为它对环境影响小,而且通过改变手性表面活性剂头基中的氨基酸可以很容易地调节其性质。利用分子动力学模拟来研究AABMM的结构和性质是一项正在进行的研究的一部分,重点是研究和阐明与AABMM手性识别有关的因素。研究结果将有助于合理设计和选择更高效的手性选择剂。所研究的胶束含有大约20个共价连接的表面活性剂单体。每个单体依次由一个十一烷基烃链组成,该链与包含l -丙氨酸、l -缬氨酸和l -亮氨酸的所有组合的二肽头基结合。这些材料之所以引起人们的兴趣,是因为它们是毛细管电泳分离中有效的手性选择剂。采用分子动力学模拟方法研究了头基氨基酸r基团的大小和位置对各AABMM手性中心溶剂可及表面积的影响。此外,采用头基二面角分析研究了氨基酸r基大小和位置对整个头基构象的影响。最后,通过距离测量来研究每个AABMM头组的结构和构象灵活性。所有分析都是在一个更广泛的研究背景下进行的,该研究的重点是开发基于结构的预测工具,以确定(a)自组装、(b)功能、(c)高阶结构和(d)这些基于氨基酸的分子胶束的分子识别的因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterization of Amino Acid Based Molecular Micelles with Molecular Modeling.

The enantiomers of chiral drugs often have different potencies, toxicities, and biochemical properties. Therefore, the FDA and other worldwide regulatory agencies require manufactures to test and prove the enantiomeric purity of chiral drugs. Amino acid based molecular micelles (AABMM) have been used in chiral CE separations since the 1990's because of their low environmental impact and because their properties can easily be tuned by changing the amino acids in the chiral surfactant headgroups. Using molecular dynamics simulations to investigate the structures and properties of AABMM is part of an ongoing study focusing on investigating and elucidating the factors responsible for chiral recognition with AABMM. The results will be useful for the proper design and selection of more efficient chiral selectors. The micelles investigated contained approximately twenty covalently linked surfactant monomers. Each monomer was in turn composed of an undecyl hydrocarbon chain bound to a dipeptide headgroup containing of all combinations of L-Alanine, L-Valine, and L-Leucine. These materials are of interest because they are effective chiral selectors in capillary electrophoresis separations. Molecular dynamics simulation analyses were used to investigate how the sizes and positions of the headgroup amino acid R-groups affected the solvent accessible surface areas of each AABMM chiral center. In addition, headgroup dihedral angle analyses were used to investigate how amino acid R-group size and position affected the overall headgroup conformations. Finally, distance measurements were used to study the structural and conformational flexibilities of each AABMM headgroup. All analyses were performed in the context of a broader study focused on developing structure-based predictive tools to identify the factors responsible for (a) self-assembly, (b) function, (c) higher ordered structure and (d) molecular recognition of these amino acid based molecular micelles.

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