Tripet Brian, Cepeniene Dziuleta, Kovacs James M, Mant Colin T, Krokhin Oleg V, Hodges Robert S
Department of Biochemistry and Molecular Genetics, University of Colorado at Denver and Health Sciences Center, Aurora, CO 80045, USA.
J Chromatogr A. 2007 Feb 9;1141(2):212-25. doi: 10.1016/j.chroma.2006.12.024. Epub 2006 Dec 21.
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(alpha)-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.
通过准确预测已知组成肽段的保留时间,反相高效液相色谱(RP-HPLC)的价值和蛋白质组学领域将得到极大提升。本研究调查了肽段N端和C端氨基酸侧链的亲水性/疏水性,同时改变了末端的官能团。我们在一个模型肽序列的N端和C端替换了所有20种天然存在的氨基酸,其中N端的官能团为N(α)-乙酰基-X-和N(α)-氨基-X-,C端的官能团为-X-C(α)-羧基和-X-C(α)-酰胺。随后从这些肽段的RP-HPLC保留行为中得出氨基酸系数,并相互比较,同时与在肽链中心确定的系数(内部系数)进行比较。对于疏水侧链,C端取代残基产生的系数差异最大(在-X-C(α)-羧基和-X-C(α)-酰胺肽系列之间)。在N(α)-乙酰基-X-和N(α)-氨基-X-肽系列中也观察到了类似的结果,其中疏水侧链的系数值差异最大。与疏水侧链的内部系数相比,C端疏水氨基酸取代产生的系数差异显著,从色氨酸的17.1分钟到半胱氨酸的4.8分钟不等。相比之下,N端取代产生的系数与内部系数的差异相对较小。随后通过使用内部系数和C端残基系数相结合的预测算法,在仅0.4分钟的误差范围内实现了肽段保留时间的预测。对于肽段保留时间的预测,系数之和必须包括内部系数和末端系数。