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弱结合多肽聚阳离子复合物的电子捕获解离

Electron capture dissociation of weakly bound polypeptide polycationic complexes.

作者信息

Haselmann Kim F, Jørgensen Thomas J D, Budnik Bogdan A, Jensen Frank, Zubarev Roman A

机构信息

Department of Chemistry, University of Southern Denmark, Odense, Denmark.

出版信息

Rapid Commun Mass Spectrom. 2002;16(24):2260-5. doi: 10.1002/rcm.853.

Abstract

We have previously reported that, in electron capture dissociation (ECD), rupture of strong intramolecular bonds in weakly bound supramolecular aggregates can proceed without dissociation of weak intermolecular bonds. This is now illustrated on a series of non-specific peptide-peptide dimers as well as specific complexes of modified glycopeptide antibiotics with their target peptide. The weak nature of bonding is substantiated by blackbody infrared dissociation, low-energy collisional excitation and force-field simulations. The results are consistent with a non-ergodic ECD cleavage mechanism.

摘要

我们之前曾报道过,在电子捕获解离(ECD)过程中,弱结合超分子聚集体中强分子内键的断裂可以在不破坏弱分子间键的情况下进行。现在,这一点在一系列非特异性肽 - 肽二聚体以及修饰的糖肽抗生素与其靶肽的特异性复合物中得到了证明。通过黑体红外解离、低能碰撞激发和力场模拟证实了键的弱性质。结果与非遍历ECD裂解机制一致。

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