Investigation of b^sub n^-44 Peptide Fragments Using High Resolution Mass Spectrometry and Isotope Labeling

• Published in: Journal of the American Society for Mass Spectrometry Vol. 25; no. 12; p. 2116
• Main Authors: Wang, Bing, Yu, Jiayi, Wang, Huixin, Wei, Zhonglin, Guo, Xinhua, Xiao, Zhaohui, Zeng, Zhoufang, Kong, Wei
• Format: Journal Article
• Language: English
• Published: New York Springer Nature B.V 01.12.2014
• Subjects: Biomedical materials; Carbon dioxide; Density functional theory; Fragmentation; Fragments; High resolution; Ions; Labeling; Mass spectrometry; Peptides; Scientific imaging; Spectroscopy; Surgical implants
• ISSN: 1044-0305; 1879-1123
• DOI: 10.1007/s13361-014-0994-9

An N-terminal deuterohemin-containing hexapeptide (DhHP-6) was designed as a short peptide cytochrome c (Cyt c) mimetic to study the effect of N-terminal charge on peptide fragmentation pathways. This peptide gave different dissociation patterns than normal tryptic peptides. Upon collision-induced dissociation (CID) with an ion trap mass spectrometer, the singly charged peptide ion containing no added proton generated abundant and characteristic bn-44 ions instead of bn-28 (an) ions. Studies by high resolution mass spectrometry (HRMS) and isotope labeling indicate that elimination of 44 Da fragments from b ions occurs via two different pathways: (1) loss of CH3CHO (44.0262) from a Thr side chain; (2) loss of CO2 (43.9898) from the oxazolone structure in the C-terminus. A series of analogues were designed and analyzed. The experimental results combined with Density Functional Theory (DFT) calculations on the proton affinity of the deuteroporphyrin demonstrate that the production of these novel bn-44 ions is related to the N-terminal charge via a charge-remote rather than radical-directed fragmentation pathway. [Figure not available: see fulltext.]