H-Tyr-His-OH was maintained as an internal standard for histidine quantitative analysis and eluted at 8.06 min. In addition, since it does not exist in tissues as an endogenous peptide, it is easy to form positive ions through ESI ionization, with good recovery.[1,2]
References:
[1]: Aldini G, Orioli M,et,al. Profiling histidine-containing dipeptides in rat tissues by liquid chromatography/electrospray ionization tandem mass spectrometry. J Mass Spectrom. 2004 Dec;39(12):1417-28. doi: 10.1002/jms.696. PMID: 15578740.
[2]: Orioli M, Aldini G, et,al. LC-ESI-MS/MS determination of 4-hydroxy-trans-2-nonenal Michael adducts with cysteine and histidine-containing peptides as early markers of oxidative stress in excitable tissues. J Chromatogr B Analyt Technol Biomed Life Sci. 2005 Nov 15;827(1):109-18. doi: 10.1016/j.jchromb.2005.04.025. PMID: 15916929.
H-Tyr-His-OH 作为组氨酸定量分析的内标,并在 8.06 分钟时洗脱。此外,由于它不作为内源性肽存在于组织中,通过ESI电离很容易形成正离子,回收率好。[1,2]
















