Evidence map›Paper›PMID 26122519›Full record

ArticleJournal of the American Society for Mass Spectrometry2015

Investigations of Some Liquid Matrixes for Analyte Quantification by MALDI.

Jeong Hee Moon, Kyung Man Park, Sung Hee Ahn, Seong Hoon Lee, Myung Soo Kim

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Article in Journal of the American Society for Mass Spectrometry, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Jeong Hee MoonFunctional Genomics Research Center, KRIBB, Daejeon, 305-806, Korea.
Kyung Man ParkDepartment of Chemistry, Seoul National University, Seoul, 151-747, Korea.
Sung Hee AhnDepartment of Chemistry, Seoul National University, Seoul, 151-747, Korea.
Seong Hoon LeeDepartment of Chemistry, Seoul National University, Seoul, 151-747, Korea.
Myung Soo KimSeoul National University Research Institute for Basic Sciences, Seoul, 151-747, Korea. myungsoo@snu.ac.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sample inhomogeneity is one of the obstacles preventing the generation of reproducible mass spectra by MALDI and to their use for the purpose of analyte quantification. As a potential solution to this problem, we investigated MALDI with some liquid matrixes prepared by nonstoichiometric mixing of acids and bases. Out of 27 combinations of acids and bases, liquid matrixes could be produced from seven. When the overall spectral features were considered, two liquid matrixes using α-cyano-4-hydroxycinnamic acid as the acid and 3-aminoquinoline and N,N-diethylaniline as bases were the best choices. In our previous study of MALDI with solid matrixes, we found that three requirements had to be met for the generation of reproducible spectra and for analyte quantification: (1) controlling the temperature by fixing the total ion count, (2) plotting the analyte-to-matrix ion ratio versus the analyte concentration as the calibration curve, and (3) keeping the matrix suppression below a critical value. We found that the same requirements had to be met in MALDI with liquid matrixes as well. In particular, although the liquid matrixes tested here were homogeneous, they failed to display spot-to-spot spectral reproducibility unless the first requirement above was met. We also found that analyte-derived ions could not be produced efficiently by MALDI with the above liquid matrixes unless the analyte was sufficiently basic. In this sense, MALDI processes with solid and liquid matrixes should be regarded as complementary techniques rather than as competing ones.

Indexed as

AminoquinolinesAniline CompoundsCalibrationCoumaric AcidsModels, ChemicalReproducibility of ResultsSpectrometry, Mass, Matrix-Assisted Laser Desorption-Ionizationalpha-cyano-4-hydroxycinnamateAminoquinolinesAniline CompoundsCoumaric AcidsN,N-diethylaniline3AQ/CHCALiquid matrixMALDIMALDI quantificationMALDI temperatureMatrix suppressionReproducible MALDI

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.