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B. M. Peek, G. T. Ross, S. W. Edwards, G. J. Meyer, et al., “Synthesis of Redox Derivatives of Lysine and Related Peptides Containing Phenothiazine or Tris(2,2'-bipyridine)ruthenium(II),” International Journal of Peptide and Protein Research, Vol. 38, No. 2, 1991, pp. 114-123. doi:10.1111/j.1399-3011.1991.tb01418.x
has been cited by the following article:
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TITLE:
A New Metal Tag for Highly Selective and Sensitive Analyses of Amino Acids and Dipeptides by HPLC/ICP-MS
AUTHORS:
Daigo Iwahata, Kazuki Nakamura, Rie Yamada, Hiroshi Miyano, Naoyuki Yamada
KEYWORDS:
Metal Tag; HPLC/ICP-MS; Amino Acid; Dipeptide; Derivatization; Speciation
JOURNAL NAME:
Journal of Analytical Sciences, Methods and Instrumentation,
Vol.3 No.2,
May
31,
2013
ABSTRACT: We have developed a novel metal tag, bis(ethylenediamine)-4'-methyl-4-carboxybipyridine-ruthenium N-succinimidyl ester (ECRS) for sensitive analysis of amino acids using high performance liquid chromatography/inductively coupled plasma mass spectrometry (HPLC/ICP-MS). ECRS is a functional reagent, containing an ester group at one end that can be activated to bind to amino group and a chelated ruthenium at the other. The activated ester was reacted briefly with amino groups under weakly alkaline conditions. The ruthenium was detected sensitively by ICP-MS. ECRS was reacted with 17 proteinogenic amino acids in borate buffer. The derivatives were separated by reversed phase HPLC and identified by quadrupole-based ICP-MS. ECRS was suitable for speciation; low molecular weight compounds containing amino groups. We have thus established a quantitative analytical method for amino acids and dipeptides. The detection limits of branched amino acids (signal-to-noise ratio of 3) were 1.5 nmol·L-1 in the standard solution (100 amol per injection).