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含脯氨酸的肽离子的气相构象特异性光解。

Gas-phase conformation-specific photofragmentation of proline-containing peptide ions.

机构信息

Department of Chemistry, Indiana University, Bloomington, Indiana, USA.

出版信息

J Am Soc Mass Spectrom. 2010 Aug;21(8):1455-65. doi: 10.1016/j.jasms.2010.04.007. Epub 2010 Apr 18.

Abstract

Singly-protonated proline-containing peptides with N-terminal arginine are photodissociated with vacuum ultraviolet (VUV) light in an ESI linear ion trap/orthogonal-TOF (LIT/o-TOF). When proline is the nth residue from the N-terminus, unusual b(n) + 2 and a(n) + 2 ions are observed. Their formation is explained by homolytic cleavage of the C(alpha)-C bond in conjunction with a rearrangement of electrons and an amide hydrogen. The latter is facilitated by a proline-stabilized gas-phase peptide conformation.

摘要

含单质子化脯氨酸的 N-端精氨酸肽在 ESI 线性离子阱/正交-TOF(LIT/o-TOF)中用真空紫外(VUV)光光解。当脯氨酸是从 N-末端的第 n 个残基时,会观察到不寻常的 b(n) + 2 和 a(n) + 2 离子。它们的形成是通过 C(alpha)-C 键的均裂以及电子和酰胺氢的重排来解释的。后者是由脯氨酸稳定的气相肽构象促进的。

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