Kwantwi-Barima Pearl, Hogan Christopher J, Clowers Brian H
Department of Chemistry, Washington State University, Pullman, Washington 99164, United States.
Department of Mechanical Engineering, University of Minnesota, Minneapolis, Minnesota 55455, United States.
J Am Soc Mass Spectrom. 2020 Sep 2;31(9):1803-1814. doi: 10.1021/jasms.0c00020. Epub 2020 Aug 10.
Vapor assisted mobility shift measurements were made with atmospheric pressure drift-tube ion mobility-mass spectrometry (IM-MS) to determine the thermodynamic properties of weakly bound ion-molecule clusters formed from protonated phenylalanine and neutral vapor molecules with hydroxyl functional groups. Relative binding energies and gas-phase association energies of amino acid ions clustered with small organic molecules have been established previously using high-pressure mass spectrometry. However, the issue of volatility largely prohibits the use of high-pressure mass spectrometry for the determination of gas-phase associations of amino acid ions clustered with neutral vapor molecules in many instances. In contrast, ion mobility measurements can be made at atmospheric pressure with volatile vapor additives near and above their boiling points, providing access to clustering equilibria not possible using high-vacuum techniques. In this study, we report the gas-phase association energies, enthalpies, and entropies for a protonated phenylalanine ion clustered with three neutral vapor molecules: 2-propanol, 1-butanol, and 2-pentanol based upon measurements at temperatures ranging from 120 to 180 °C. The gas-phase enthalpy and entropy changes ranged between -4 to -7 kcal/mol and -3 to 6 cal/(mol K), respectively. We found enthalpically favored ion-neutral cluster reactions for phenylalanine with entropic barriers for the formation of phenylalanine-1-butanol and phenylalanine-2-pentanol cluster ions, while phenylalanine-2-propanol cluster ion formation is both enthalpically and (weakly) entropically favorable. Under the measurement conditions examined, phenylalanine-vapor modifier cluster ion formation is clearly observed via shifts in the drift time for the three test vapor molecules. In comparison, negligible shifts in mobility are observed for protonated arginine exposed to the same vapor modifiers.
采用常压漂移管离子迁移率-质谱联用技术(IM-MS)进行了蒸汽辅助迁移率变化测量,以确定由质子化苯丙氨酸与含羟基官能团的中性蒸汽分子形成的弱结合离子-分子簇的热力学性质。此前已利用高压质谱法确定了氨基酸离子与小有机分子形成的簇的相对结合能和气相缔合能。然而,在许多情况下,挥发性问题在很大程度上限制了使用高压质谱法来测定氨基酸离子与中性蒸汽分子形成的气相缔合。相比之下,离子迁移率测量可在常压下使用接近或高于其沸点的挥发性蒸汽添加剂进行,从而能够获得使用高真空技术无法实现的簇集平衡。在本研究中,我们报告了基于在120至180°C温度范围内的测量结果,质子化苯丙氨酸离子与三种中性蒸汽分子(2-丙醇、1-丁醇和2-戊醇)形成的簇的气相缔合能、焓和熵。气相焓变和熵变分别在-4至-7 kcal/mol和-3至6 cal/(mol·K)之间。我们发现苯丙氨酸的离子-中性簇反应在焓上是有利的,但形成苯丙氨酸-1-丁醇和苯丙氨酸-2-戊醇簇离子存在熵垒,而苯丙氨酸-2-丙醇簇离子的形成在焓和(弱)熵上都是有利的。在所研究的测量条件下,通过三种测试蒸汽分子的漂移时间变化清晰地观察到了苯丙氨酸-蒸汽改性剂簇离子的形成。相比之下,暴露于相同蒸汽改性剂的质子化精氨酸的迁移率变化可忽略不计。