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Nucleic Acids Research, 2001, Vol. 29, No. 19 e91
© 2001 Oxford University Press

Sugar additives for MALDI matrices improve signal allowing the smallest nucleotide change (A:T) in a DNA sequence to be resolved

Mona Shahgholi1, Benjamin A. Garcia1, Norman H. L. Chiu1,2, Paul J. Heaney1 and Kai Tang1,*

1Sequenom Inc., 3595 John Hopkins Court, San Diego, CA 92121, USA and 2Center for Advanced Biotechnology, Boston University, Boston, MA 02215, USA

Sample preparation for matrix-assisted laser desorption/ionization (MALDI) mass spectrometry (MS) of DNA is critical for obtaining high quality mass spectra. Sample impurity, solvent content, substrate surface and environmental conditions (temperature and humidity) all affect the rate of matrix–analyte co-crystallization. As a result, laser fluence threshold for desorption/ionization varies from spot to spot. When using 3-hydroxypicolinic acid (3-HPA) as the matrix, laser fluence higher than the threshold value reduces mass resolution in time-of-flight (TOF) MS as the excess energy transferred to DNA causes metastable decay. This can be overcome by either searching for ‘hot’ spots or adjusting the laser fluence. However, both solutions may require a significant amount of operator manipulation and are not ideal for automatic measurements. We have added various sugars for crystallization with the matrix to minimize the transfer of excess laser energy to DNA molecules. Fructose and fucose were found to be the most effective matrix additives. Using these additives, mass resolution for DNA molecules does not show noticeable deterioration as laser energy increases. Improved sample preparation is important for the detection of single nucleotide polymorphisms (SNPs) using primer extension with a single nucleotide. During automatic data acquisition it is difficult to routinely detect heterozygous A/T mutations, which requires resolving a mass difference of 9 Da, unless a sugar is added during crystallization.

* To whom correspondence should be addressed: Tel: +1 858 202 9089; Fax: +1 858 202 9001; Email: ktang{at}sequenom.com Present address:Mona Shahgholi, Department of Chemistry, California Institute of Technology, 1200 East California Boulevard, Pasadena, CA 91125, USA


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