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自旋捕获封端肽中的电子捕获。肽阳离子自由基中遍历解离的一个实验示例。

Electron capture in spin-trap capped peptides. An experimental example of ergodic dissociation in peptide cation-radicals.

作者信息

Jones Jace W, Sasaki Tomikazu, Goodlett David R, Turecek Frantisek

机构信息

Department of Chemistry and Medicinal Chemistry, University of Washington, Seattle, Washington 98195-1700, USA.

出版信息

J Am Soc Mass Spectrom. 2007 Mar;18(3):432-44. doi: 10.1016/j.jasms.2006.10.005. Epub 2006 Nov 16.

Abstract

Electron capture dissociation was studied with tetradecapeptides and pentadecapeptides that were capped at N-termini with a 2-(4'-carboxypyrid-2'-yl)-4-carboxamide group (pepy), e.g., pepy-AEQLLQEEQLLQEL-NH(2), pepy-AQEFGEQGQKALKQL-NH(2), and pepy-AQEGSEQAQKFFKQL-NH(2). Doubly and triply protonated peptide cations underwent efficient electron capture in the ion-cyclotron resonance cell to yield charge-reduced species. However, the electron capture was not accompanied by backbone dissociations. When the peptide ions were preheated by absorption of infrared photons close to the dissociation threshold, subsequent electron capture triggered ion dissociations near the remote C-terminus forming mainly (b(11-14) + 1)(+)* fragment ions that were analogous to those produced by infrared multiphoton dissociation alone. Ab initio calculations indicated that the N-1 and N-1' positions in the pepy moiety had topical gas-phase basicities (GB = 923 kJ mol(-1)) that were greater than those of backbone amide groups. Hence, pepy was a likely protonation site in the doubly and triply charged ions. Electron capture in the protonated pepy moiety produced the ground electronic state of the charge-reduced cation-radical with a topical recombination energy, RE = 5.43-5.46 eV, which was greater than that of protonated peptide residues. The hydrogen atom in the charge-reduced pepy moiety was bound by >160 kJ mol(-1), which exceeded the hydrogen atom affinity of the backbone amide groups (21-41 kJ mol(-1)). Thus, the pepy moiety functioned as a stable electron and hydrogen atom trap that did not trigger radical-type dissociations in the peptide backbone that are typical of ECD. Instead, the internal energy gained by electron capture was redistributed over the peptide moiety, and when combined with additional IR excitation, induced proton-driven ion dissociations which occurred at sites that were remote from the site of electron capture. This example of a spin-remote fragmentation provided the first clear-cut experimental example of an ergodic dissociation upon ECD.

摘要

利用用2-(4'-羧基吡啶-2'-基)-4-羧酰胺基团(pepy)封端N端的十四肽和十五肽研究了电子捕获解离,例如,pepy-AEQLLQEEQLLQEL-NH₂、pepy-AQEFGEQGQKALKQL-NH₂和pepy-AQEGSEQAQKFFKQL-NH₂。双质子化和三质子化的肽阳离子在离子回旋共振池中经历了有效的电子捕获,产生了电荷减少的物种。然而,电子捕获并没有伴随着主链解离。当肽离子通过吸收接近解离阈值的红外光子进行预热时,随后的电子捕获触发了远离C端的离子解离,主要形成(b₁₁₋₁₄ + 1)⁺*碎片离子,这些离子类似于仅由红外多光子解离产生的离子。从头算计算表明,pepy部分中的N-1和N-1'位置具有局部气相碱度(GB = 923 kJ mol⁻¹),大于主链酰胺基团的碱度。因此,pepy是双电荷和三电荷离子中可能的质子化位点。质子化的pepy部分中的电子捕获产生了电荷减少的阳离子自由基的基态电子态,其局部重组能RE = 5.43 - 5.46 eV,大于质子化肽残基的重组能。电荷减少的pepy部分中的氢原子以>160 kJ mol⁻¹的键合,超过了主链酰胺基团的氢原子亲和力(21 - 41 kJ mol⁻¹)。因此,pepy部分起到了稳定的电子和氢原子陷阱的作用,不会触发ECD典型的肽主链中的自由基型解离。相反,通过电子捕获获得的内能在肽部分重新分布,并且当与额外的红外激发结合时,诱导质子驱动的离子解离,这些解离发生在远离电子捕获位点的位置。这种自旋远程碎片化的例子提供了ECD时遍历解离的第一个明确的实验例子。

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