Publication | Closed Access
MALDI on a Chip: Analysis of Arrays of Low-Femtomole to Subfemtomole Quantities of Synthetic Oligonucleotides and DNA Diagnostic Products Dispensed by a Piezoelectric Pipet
190
Citations
22
References
1997
Year
EngineeringMicroscopyAnalytical MicrosystemsDna AnalysisBiological Mass SpectrometryMolecular BiologyBiomedical EngineeringSynthetic OligonucleotidesSpectrochemical AnalysisSubfemtomole QuantitiesDna NanotechnologyAnalytical InstrumentationBioanalysisAnalytical ChemistryClinical ChemistryAnalytical BiotechnologyMolecular DiagnosticsBiophysicsOligonucleotideDna ReplicationMass SpectraBiomedical AnalysisPiezoelectric PipetBiomolecular EngineeringBiomedical DiagnosticsSpectroscopyMass SpectrometryBiotechnologySynthetic BiologyGenetic EngineeringMedicineGenome Editing
A piezoelectric pipet is used to dispense arrays of low-nanoliter aliquots of matrix and DNA into individual etched wells on <1 in.2 silicon chips prior to their semiautomated analysis by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). Spectrum acquisition is expedited relative to conventional “large-spot” MALDI since the resulting miniaturized samples are approximately the same size as the irradiation area of the ionization/desorption laser; thus, searching for crystal regions from which intense analyte signals may be obtained is not necessary. Using a linear TOF instrument designed for scanning high-density arrays of samples, mass spectra from as little as 0.2 fmol (45 nM) of a 36-mer DNA have been acquired from single miniature elements. Spot-to-spot reproducibility from microdispensed samples is superior to that using conventional pipets; in less than 6 min, spectra with high signal-to-noise ratios were acquired from 100 elements containing 8 fmol of a 25-mer. Low-nanoliter quantities of DNA diagnostic products generated in primer oligo base extension reactions from PCR templates were transferred to chips and analyzed by MALDI-TOF MS, giving accurate genotyping results for single base mutations and short tandem repeat polymorphisms (microsatellites). These procedures provide enabling capabilities for extremely accurate high-throughput DNA diagnostics and sequencing based on mass spectrometry.
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