American Journal of Analytical Chemistry

Volume 3, Issue 12 (December 2012)

ISSN Print: 2156-8251   ISSN Online: 2156-8278

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Acylhydrazide and Isatin Schiff Bases as Alternate UV-Laser Desorption Ionization (LDI) Matrices for Low Molecular Weight (LMW) Peptides Analysis

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DOI: 10.4236/ajac.2012.312104    4,312 Downloads   7,196 Views  Citations

ABSTRACT

Matrix-assisted laser desorption/ionization (MALDI) is a preferred and widely used mass spectrometric technique for the analysis of macromolecules. Limited UV-LDI matrices are available for the analysis of biomolecules due to the restricted structural features to serve in the laser desorption/ionization mechanism with a problem of background signals appearing in the low mass region. This paper describes the application of Schiff base derivatives of acylhydrazide and isatin as alternate UV-LDI matrices for the analysis of peptides with significantly low background signals. Thirty one compounds have been successfully employed as matrices for the analysis of low molecular weight (LMW) peptides (<2000 Da) including bradykinin and renin substrate tetra-decapeptide. Bovine serum albumin (BSA)-digest was also analyzed and identified through database search against Swiss-Prot by using MASCOT. The MS measurements were recorded by using dried droplet sample preparation procedures by mixing the matrix solution with analyte at a volume ratio of 1:2. Finally, LMW organic compounds (<500 Da) were also analyzed by the synthesized matrix materials which showed better S/N ratios and minimal background signals for low mass range in comparison to the comparable results with α-Cyano-4-hydroxycinnamic acid (HCCA), a preferred choice for peptide analysis.

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S. Musharraf, A. Bibi, N. Shahid, M. Najam-ul-Haq, M. Khan, M. Taha, U. Mughal and K. Khan, "Acylhydrazide and Isatin Schiff Bases as Alternate UV-Laser Desorption Ionization (LDI) Matrices for Low Molecular Weight (LMW) Peptides Analysis," American Journal of Analytical Chemistry, Vol. 3 No. 12, 2012, pp. 779-789. doi: 10.4236/ajac.2012.312104.

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