CYCLONE-A Utility for De Novo Sequencing of Microbial Cyclic Peptides

被引:13
|
作者
Kavan, Daniel [1 ,2 ]
Kuzma, Marek [1 ]
Lemr, Karel [1 ,3 ]
Schug, Kevin A. [4 ]
Havlicek, Vladimir [1 ,3 ]
机构
[1] Inst Microbiol, Vvi, CZ-14220 Prague 4, Czech Republic
[2] Charles Univ Prague, Fac Sci, Dept Biochem, Prague 12740 2, Czech Republic
[3] Palacky Univ, Fac Sci, Dept Analyt Chem, RCPTM, Olomouc 77146, Czech Republic
[4] Univ Texas Arlington, Dept Chem & Biochem, Arlington, TX 76019 USA
关键词
Peptide; Cyclic; Sequencing; Nonribosomal; Scrambling; Natural product; TANDEM MASS-SPECTROMETRY; NONRIBOSOMAL PEPTIDES; PROTONATED PEPTIDES; FRAGMENTATION PATHWAYS; ION-TRAP; SPECTRA; IDENTIFICATION; DATABASE;
D O I
10.1007/s13361-013-0652-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
We have developed a de novo sequencing software tool (CYCLONE) and applied it for determination of cyclic peptides. The program uses a non-redundant database of 312 nonribosomal building blocks identified to date in bacteria and fungi (more than 230 additional residues in the database list were isobaric). The software was used to fully characterize the tandem mass spectrum of several cyclic peptides and provide sequence tags. The general strategy of the script was based on fragment ion pre-characterization to accomplish unambiguous b-ion series assignments. Showcase examples were a cyclic tetradepsipeptide beauverolide, a cyclic hexadepsipeptide roseotoxin A, a lasso-like hexapeptide pseudacyclin A, and a cyclic undecapeptide cyclosporin A. The extent of ion scrambling in smaller peptides was as low as 5 % of total ion current; this demonstrated the feasibility of CYCLONE de novo sequencing. The robustness of the script was also tested against database sets of various sizes and isotope-containing data. It can be downloaded from the http://ms.biomed.cas.cz/MSTools/ website.
引用
收藏
页码:1177 / 1184
页数:8
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