Requirements for prediction of peptide retention time in reversed-phase high-performance liquid chromatography: Hydrophilicity/hydrophobicity of side-chains at the N- and C-termini of peptides are dramatically affected by the end-groups and location

被引:53
作者
Tripet, Brian
Cepeniene, Dziuleta
Kovacs, James M.
Mant, Colin T.
Krokhin, Oleg V.
Hodges, Robert S. [1 ]
机构
[1] Univ Colorado, Dept Biochem & Mol Genet, Aurora, CO 80045 USA
[2] Hlth Sci Ctr, Aurora, CO 80045 USA
[3] Univ Manitoba, Manitoba Ctr Proteom & Syst Biol, Winnipeg, MB R3T 2N2, Canada
关键词
reversed-phase high-performance liquid chromatography; prediction of peptide retention behaviour; amino acid coefficients; N-terminal coefficients; C-terminal coefficients; internal coefficients;
D O I
10.1016/j.chroma.2006.12.024
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The value of reversed-phase high-performance liquid chromatography (RP-HPLC) and the field of proteomics would be greatly enhanced by accurate prediction of retention times of peptides of known composition. The present study investigates the hydrophilicity/hydrophobicity of amino acid side-chains at the N- and C-termini of peptides while varying the functional end-groups at the termini. We substituted all 20 naturally occurring amino acids at the N- and C-termini of a model peptide sequence, where the functional end-groups were N-alpha-acetyl-X- and N-alpha-amino-X- at the N-terminus and -X-C-alpha-carboxyl and -X-C-alpha-amide at the C-terminus. Amino acid coefficients were subsequently derived from the RP-HPLC retention behaviour of these peptides and compared to each other as well as to coefficients determined in the centre of the peptide chain (internal coefficients). Coefficients generated from residues substituted at the C-terminus differed most (between the -X-C-alpha-carboxyl and -X-C-alpha-amide peptide series) for hydrophobic side-chains. A similar result was seen for the N-alpha-acetyl-X- and N'-amino-X-peptide series, where the largest differences in coefficient values were observed for hydrophobic side-chains. Coefficients derived from substitutions at the C-terminus for hydrophobic amino acids were dramatically different compared to internal coefficients for hydrophobic side-chains, ranging from 17.1 min for Trp to 4.8 min for Cys. In contrast, coefficients derived from substitutions at the N-terminus showed relatively small differences from the internal coefficients. Subsequent prediction of peptide retention time, within an error of just 0.4 min, was achieved by a predictive algorithm using a combination of internal coefficients and coefficients for the C-terminal residues. For prediction of peptide retention time, the sum of the coefficients must include internal and terminal coefficients. (c) 2006 Elsevier B.V. All fights reserved.
引用
收藏
页码:212 / 225
页数:14
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