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Thermal Decomposition of a Gaseous Multiprotein Complex Studied by Blackbody Infrared Radiative Dissociation, Investigating the Origin of the Asymmetric Dissociation Behavior

机译:黑体红外辐射解离研究气态多蛋白复合物的热分解,研究不对称解离行为的起源

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The blackbody infrared radiative dissociation technique was used to study the thermal decomposition of the gaseous B_(5) pentamer of the Shiga-like toxin I and its complexes with the P~(k) trisaccharide and a decavalent P~(k)-based oligosaccharide ligand (STARFISH, S). Dissociation of the protonated pentamer, (B_(5)+nH)~(n+)≡(B_(5))~(n+) where n=11-14, proceeds almost exclusively by the loss of a single subunit (B) with a disproportionately large fraction (30-50%) of the parention charge. The degree of charge enrichment of the leaving subunit increases with increasing parent ion charge state. For n=12-14, a distribution of product ion charge states is observed. The yields of the complementary pairs of product ions are sensitive to the reaction temperature, with higher temperatures favoring greater charge enrichment of the leaving subunit for +13 and +14, and the opposite effect for +12. These results indicate that some of the protons are rapidly exchanged between subunits in the gas phase. Dissociation of (B_(5))~(14+)·S proceeds exclusively by the loss of one subunit, although the ligand increases the stability of the complex and also reduces the degree of charge enrichment in the ejected monomer. For (B_(5))~(12+)(P~(k))_(1-3), the loss of neutral P~(k) competes with loss of a subunit at low temperatures, Linear Arrhenius plots were obtained from the temperature-dependent dissociation rate constants measured for the loss of B from (B_(5))~(n+) and (B_(5))~(14+)·S. The magnitude of the Arrhenius parameters is highly dependent on the charge state of the pentamer: E_(a)=35 kcal/mol and A=10~(19) s~(-1) (+14), 46 kcal/mol and 10~(23) s~(-1) (+13), 50 kcal/mol and 10~(26) s~(-1) (+12), and 80 kcal/mol and 10~(39) (+11). The E_(a) and A for (B_(5))~(14+)·S are 59 kcal/mol and 10~(30) s~(-1), respectively. The reaction pathways leading to greater charge enrichment of the subunit lost from the (B_(5))~(14+) and (B_(5))~(13+) ions correspond to higher energy processes, however, these pathways are kinetically preferred at higher temperatures due to their large A factors. A simple electrostatic model, whereby charge enrichment leads to Coulombic repulsion-induced denaturation of the subunits and disruption of the intersubunit interactions, provides an explanation for the magnitude of the Arrhenius parameters and the origin of the asymmetric dissociation behavior of the complexes.
机译:使用黑体红外辐射解离技术研究志贺样毒素I的气态B_(5)五聚体及其与P〜(k)三糖和十价P〜(k)基寡糖的配合物的热分解配体(STARFISH,S)。质子化五聚体(B_(5)+ nH)〜(n +)≡(B_(5))〜(n +)(其中n = 11-14)的解离几乎完全是由于单个亚基(B)的损失不成比例的大部分(30-50%)的亲子电荷。离开的亚基的电荷富集程度随着母体离子电荷状态的增加而增加。对于n = 12-14,观察到产物离子电荷态的分布。互补产物离子对的产率对反应温度敏感,较高的温度有利于+13和+14的离去亚基具有更大的电荷富集,而对于+12则相反。这些结果表明,一些质子在气相的亚基之间快速交换。 (B_(5))〜(14+)·S的解离仅通过一个亚基的损失而进行,尽管配体增加了配合物的稳定性并降低了喷射单体中电荷的富集程度。对于(B_(5))〜(12 +)(P〜(k))_(1-3),在低温下中性P〜(k)的损失与亚基的损失竞争,获得线性阿伦尼乌斯图从针对(B_(5))〜(n +)和(B_(5))〜(14+)·S中的B损失测得的温度依赖性解离速率常数得出。 Arrhenius参数的大小高度依赖于五聚体的电荷状态:E_(a)= 35 kcal / mol和A = 10〜(19)s〜(-1)(+14),46 kcal / mol和10〜(23)s〜(-1)(+13),50 kcal / mol和10〜(26)s〜(-1)(+12),80 kcal / mol和10〜(39)(+ 11)。 (B_(5))〜(14+)·S的E_(a)和A分别为59 kcal / mol和10〜(30)s〜(-1)。从(B_(5))〜(14+)和(B_(5))〜(13+)离子中丢失的亚基导致更大电荷富集的反应途径对应于更高的能量过程,但是这些途径在动力学上是由于其较大的A因子,因此在较高的温度下首选。一个简单的静电模型,即电荷富集导致库仑排斥引起的亚基变性和亚基间相互作用的破坏,为阿累尼乌斯参数的大小以及复合物不对称解离行为的起源提供了解释。

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