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Polyamine co-matrices for matrix-assisted laser desorption/ionization mass spectrometry of oligonucleotides.
Rapid Commun Mass Spectrom. 1999; 13(20):2014-21.RC

Abstract

The analysis of oligonucleotides using matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) has led to the investigation of the use of matrix additives (i.e., co-matrices) to help improve the poor spectral quality commonly observed during the analysis of this class of compounds. The use of certain matrix additives in MALDI-MS has been investigated previously, and these additives have been shown to enhance the desorption/ionization efficiency of oligonucleotides during the MALDI experiment. Specifically, amine bases, such as piperidine, imidazole, and triethylamine, have been shown to improve mass spectral quality as assessed by improved molecular ion resolution and increased molecular ion abundance. These improvements occur due to competition between the oligonucleotide and the co-matrix for protons generated during the MALDI event. Co-matrices with proton affinities near or above the proton affinities of the nucleotide residues serve as proton sinks during the desorption/ionization process. In this work, we have investigated the use of polyamines as co-matrices for MALDI mass spectrometric analysis of oligonucleotides. Spermine tetrahydrochloride, spermine, spermidine trihydrochloride, and spermidine were evaluated for their effectiveness at enhancing the mass spectral quality of oligonucleotides analyzed using MALDI-MS. The solution-phase pK(b) values and the gas-phase proton affinities of these polyamines were determined, and it was found that the polyamines appear to be more basic than the monofunctional amines investigated previously. The mass spectral data shows that spermidine and spermine are extremely effective co-matrices, yielding improved molecular ion resolution and molecular ion abundances. The spermine co-matrices are more effective than the spermidine co-matrices, but adduction problems with the spermine co-matrices limits their overall utility. In general, polyamine co-matrices are found to be more effective than monofunctional amine co-matrices at improving the mass spectral data obtained during MALDI-MS of oligonucleotides.

Authors+Show Affiliations

232 Choppin Hall, Department of Chemistry, Louisiana State University, Baton Rouge, LA 70803, USA.No affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, P.H.S.

Language

eng

PubMed ID

10510414

Citation

Vandell, V E., and P A. Limbach. "Polyamine Co-matrices for Matrix-assisted Laser Desorption/ionization Mass Spectrometry of Oligonucleotides." Rapid Communications in Mass Spectrometry : RCM, vol. 13, no. 20, 1999, pp. 2014-21.
Vandell VE, Limbach PA. Polyamine co-matrices for matrix-assisted laser desorption/ionization mass spectrometry of oligonucleotides. Rapid Commun Mass Spectrom. 1999;13(20):2014-21.
Vandell, V. E., & Limbach, P. A. (1999). Polyamine co-matrices for matrix-assisted laser desorption/ionization mass spectrometry of oligonucleotides. Rapid Communications in Mass Spectrometry : RCM, 13(20), 2014-21.
Vandell VE, Limbach PA. Polyamine Co-matrices for Matrix-assisted Laser Desorption/ionization Mass Spectrometry of Oligonucleotides. Rapid Commun Mass Spectrom. 1999;13(20):2014-21. PubMed PMID: 10510414.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Polyamine co-matrices for matrix-assisted laser desorption/ionization mass spectrometry of oligonucleotides. AU - Vandell,V E, AU - Limbach,P A, PY - 1999/10/8/pubmed PY - 1999/10/8/medline PY - 1999/10/8/entrez SP - 2014 EP - 21 JF - Rapid communications in mass spectrometry : RCM JO - Rapid Commun Mass Spectrom VL - 13 IS - 20 N2 - The analysis of oligonucleotides using matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) has led to the investigation of the use of matrix additives (i.e., co-matrices) to help improve the poor spectral quality commonly observed during the analysis of this class of compounds. The use of certain matrix additives in MALDI-MS has been investigated previously, and these additives have been shown to enhance the desorption/ionization efficiency of oligonucleotides during the MALDI experiment. Specifically, amine bases, such as piperidine, imidazole, and triethylamine, have been shown to improve mass spectral quality as assessed by improved molecular ion resolution and increased molecular ion abundance. These improvements occur due to competition between the oligonucleotide and the co-matrix for protons generated during the MALDI event. Co-matrices with proton affinities near or above the proton affinities of the nucleotide residues serve as proton sinks during the desorption/ionization process. In this work, we have investigated the use of polyamines as co-matrices for MALDI mass spectrometric analysis of oligonucleotides. Spermine tetrahydrochloride, spermine, spermidine trihydrochloride, and spermidine were evaluated for their effectiveness at enhancing the mass spectral quality of oligonucleotides analyzed using MALDI-MS. The solution-phase pK(b) values and the gas-phase proton affinities of these polyamines were determined, and it was found that the polyamines appear to be more basic than the monofunctional amines investigated previously. The mass spectral data shows that spermidine and spermine are extremely effective co-matrices, yielding improved molecular ion resolution and molecular ion abundances. The spermine co-matrices are more effective than the spermidine co-matrices, but adduction problems with the spermine co-matrices limits their overall utility. In general, polyamine co-matrices are found to be more effective than monofunctional amine co-matrices at improving the mass spectral data obtained during MALDI-MS of oligonucleotides. SN - 0951-4198 UR - https://www.unboundmedicine.com/medline/citation/10510414/Polyamine_co_matrices_for_matrix_assisted_laser_desorption/ionization_mass_spectrometry_of_oligonucleotides_ L2 - https://doi.org/10.1002/(SICI)1097-0231(19991030)13:20<2014::AID-RCM748>3.0.CO;2-C DB - PRIME DP - Unbound Medicine ER -