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用于确定质子化三聚体的电荷溶剂化结构与盐桥结构的离子迁移谱评估。

Evaluation of ion mobility spectroscopy for determining charge-solvated versus salt-bridge structures of protonated trimers.

作者信息

Wong Richard L, Williams Evan R, Counterman Anne E, Clemmer David E

机构信息

Department of Chemistry, University of California, Berkeley, California 94720, USA.

出版信息

J Am Soc Mass Spectrom. 2005 Jul;16(7):1009-19. doi: 10.1016/j.jasms.2005.03.029.

Abstract

The cross sections of five different protonated trimers consisting of two base molecules and trifluoroacetic acid were measured by using ion mobility spectrometry. The gas-phase basicities of these five base molecules span an 8-kcal/mol range. These cross sections are compared with those determined from candidate low-energy salt-bridge and charge-solvated structures identified by using molecular mechanics calculations using three different force fields: AMBER*, MMFF, and CHARMm. With AMBER*, the charge-solvated structures are all globular and the salt-bridge structures are all linear, whereas with CHARMm, these two forms of the protonated trimers can adopt either shape. Globular structures have smaller cross sections than linear structures. Conclusions about the structure of these protonated trimers are highly dependent on the force field used to generate low-energy candidate structures. With AMBER*, all of the trimers are consistent with salt-bridge structures, whereas with MMFF the measured cross sections are more consistent with charge-solvated structures, although the assignments are ambiguous for two of the protonated trimers. Conclusions based on structures generated by using CHARMm suggest a change in structure from charge-solvated to salt-bridge structures with increasing gas-phase basicity of the constituent bases, a result that is most consistent with structural conclusions based on blackbody infrared radiative dissociation experiments for these protonated trimers and theoretical calculations on the uncharged base-acid pairs.

摘要

利用离子迁移谱法测量了由两个碱基分子和三氟乙酸组成的五种不同质子化三聚体的横截面。这五个碱基分子的气相碱度范围为8千卡/摩尔。将这些横截面与通过使用三种不同力场(AMBER*、MMFF和CHARMm)的分子力学计算确定的候选低能盐桥和电荷溶剂化结构的横截面进行比较。使用AMBER时,电荷溶剂化结构均为球状,盐桥结构均为线性,而使用CHARMm时,这两种形式的质子化三聚体可以呈现任何一种形状。球状结构的横截面比线性结构小。关于这些质子化三聚体结构的结论高度依赖于用于生成低能候选结构的力场。使用AMBER时,所有三聚体均与盐桥结构一致,而使用MMFF时,测量的横截面与电荷溶剂化结构更一致,尽管对于其中两个质子化三聚体的归属不明确。基于使用CHARMm生成的结构得出的结论表明,随着组成碱基气相碱度的增加,结构从电荷溶剂化结构转变为盐桥结构,这一结果与基于这些质子化三聚体的黑体红外辐射解离实验和对不带电荷的碱基-酸对的理论计算得出的结构结论最为一致。

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