Analysis of dimer and trimer complexes of the non-amyloidogenic rat islet amyloid polypeptide 21-37 by electrospray ionization-tandem mass spectrometry.

IF 1.1 4区 化学 Q4 PHYSICS, ATOMIC, MOLECULAR & CHEMICAL European Journal of Mass Spectrometry Pub Date : 2024-09-05 DOI:10.1177/14690667241278462
Jin Young Lim, Seo Yeon Kim, Ho-Tae Kim
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Abstract

The dimer and trimer structures of the non-amyloidogenic rat islet amyloid polypeptide 21-37 peptide, formed in an H2O/CH3OH (1% CH3COOH) solution were investigated using electrospray ionization-tandem mass spectrometry (ESI-MS/MS). The dissociation of monomers, dimers, and trimers was investigated by MS/MS using collision-induced dissociation. The peptide bond dissociation between L7 and P8 was mainly observed in the tandem mass spectra of the monomers and oligomers, regardless of the parent ion charge state. The fragment ions were observed as a series of bu (u = 3-4, 6-7, 12) or yn (n = 10-11, 13-14) in the [Mono + 2H]2+ (=[monomer + 2H]2+) tandem mass spectrum. MS/MS analysis of the [Di + 3H]3+ (=[dimer + 3H]3+) complex indicated that [Di + 3H]3+ comprised [Mono + H]1+ and [Mono + 2H]2+ subunits. During covalent bond dissociation of the [Di + 3H]3+ complex, a fragmentation pattern was observed in the form of {mono + (fragment ion of [Mono + 2H]2+)}, resulting from the collision energy dissociation of the [Mono + 2H]2+ peptide. The [(C-terminal)-(C-terminal)] interaction geometry was proposed for the [Di + 3H]3+ complex based on the observation of [y10 + yn]2+ (n = 10-11, 13-16) fragment ions in the [Di + 3H]3+ tandem mass spectrum. MS/MS analysis of the [Tri + 4H]4+ (=[trimer + 4H]4+) complex indicated that [Tri + 4H]4+ comprised [Mono + H]1+ and [Di + 3H]3+ subunits. The (monomer-[Di + 3H]3+)4+ complex geometry was assumed to be stable based on the presence of {mono + (fragment ion of [Di + 3H]3+)} ions in the tandem mass spectrum of the [Tri + 4H]4+ complex. The two [Mono + (y10 + y10)]2+ and [Mono + (Mono + y10)]3+ fragment ions also supported the (monomer-[Di + 3H]3+)4+ complex geometries of the [Tri + 4H]4+ complex. The [(C-terminal)-(C-terminal)] interaction geometry of the [Di + 3H]3+ subunit is thought to be conserved in the [Tri + 4H]4+ complex geometries.

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电喷雾电离-串联质谱法分析非淀粉样蛋白生成的大鼠胰岛淀粉样多肽 21-37 的二聚体和三聚体复合物。
利用电喷雾离子化-串联质谱法(ESI-MS/MS)研究了在 H2O/CH3OH (1% CH3COOH)溶液中形成的非淀粉样蛋白大鼠胰岛淀粉样多肽 21-37 肽的二聚体和三聚体结构。质谱/质谱采用碰撞诱导解离法研究了单体、二聚体和三聚体的解离情况。在单体和低聚物的串联质谱中,主要观察到 L7 和 P8 之间的肽键解离,与母离子的电荷状态无关。在[单体 + 2H]2+(=[单体 + 2H]2+)串联质谱中观察到的碎片离子为一系列 bu(u = 3-4、6-7、12)或 yn(n = 10-11、13-14)。Di + 3H]3+(=[二聚体 + 3H]3+)复合物的 MS/MS 分析表明,[Di + 3H]3+由 [Mono + H]1+ 和 [Mono + 2H]2+ 亚基组成。在[Di + 3H]3+复合物的共价键解离过程中,观察到{mono +([Mono + 2H]2+的碎片离子)}形式的碎片模式,这是[Mono + 2H]2+肽的碰撞能解离产生的。根据在[Di + 3H]3+串联质谱中观察到的[y10 + yn]2+(n = 10-11,13-16)碎片离子,提出了[Di + 3H]3+复合物的[(C-末端)-(C-末端)]相互作用几何结构。对 [Tri + 4H]4+(=[三聚体 + 4H]4+)复合物的 MS/MS 分析表明,[Tri + 4H]4+ 由 [Mono + H]1+ 和 [Di + 3H]3+ 亚基组成。根据[Tri + 4H]4+复合物的串联质谱中出现的{mono +([Di + 3H]3+的碎片离子)}离子,推测(单体-[Di + 3H]3+)4+复合物的几何形状是稳定的。两个 [Mono + (y10 + y10)]2+ 和 [Mono + (Mono + y10)]3+ 片段离子也支持 [Tri + 4H]4+ 复合物的(单体-[Di + 3H]3+)4+ 复合物几何结构。据认为,[Di + 3H]3+亚基的[(C-末端)-(C-末端)]相互作用几何形状在[Tri + 4H]4+复合物几何形状中是保留的。
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来源期刊
CiteScore
2.40
自引率
7.70%
发文量
16
审稿时长
>12 weeks
期刊介绍: JMS - European Journal of Mass Spectrometry, is a peer-reviewed journal, devoted to the publication of innovative research in mass spectrometry. Articles in the journal come from proteomics, metabolomics, petroleomics and other areas developing under the umbrella of the “omic revolution”.
期刊最新文献
Exploring the versatility of mass spectrometry: Applications across diverse scientific disciplines. Analysis of dimer and trimer complexes of the non-amyloidogenic rat islet amyloid polypeptide 21-37 by electrospray ionization-tandem mass spectrometry. Clustering of biphenyl oxamide ions by chiral recognition. Concept and simulation of a novel dual-layer linear ion trap mass analyzer for micro-electromechanical systems mass spectrometry. Stereoscopic imaging of volatile organic compounds distribution in the region and tracing emission sources of volatile organic compounds using a novel movable single-photon ionization time-of-flight mass spectrometer.
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