High-resolution droplet-based fractionation of nano-LC separations onto microarrays for MALDI-MS analysis

Journal Article (2014)
Authors

Simon Karl Küster (ETH Zürich)

Martin Pabst (ETH Zürich)

Konstantins Jefimovs (Swiss Federal Laboratories for Materials Science and Technology (Empa))

Renato Zenobi (ETH Zürich)

Petra S. Dittrich (ETH Zürich)

Affiliation
External organisation
To reference this document use:
https://doi.org/10.1021/ac4041982
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Publication Year
2014
Language
English
Affiliation
External organisation
Issue number
10
Volume number
86
Pages (from-to)
4848-4855
DOI:
https://doi.org/10.1021/ac4041982

Abstract

We present a robust droplet-based device, which enables the fractionation of ultralow flow rate nanoflow liquid chromatography (nano-LC) eluate streams at high frequencies and high peak resolution. This is achieved by directly interfacing the separation column to a micro T-junction, where the eluate stream is compartmentalized into picoliter droplets. This immediate compartmentalization prevents peak dispersion during eluate transport and conserves the chromatographic performance. Subsequently, nanoliter eluate fractions are collected at a rate of one fraction per second on a high-density microarray to retain the separation with high temporal resolution. Chromatographic separations of up to 45 min runtime can thus be archived on a single microarray possessing 2700 sample spots. The performance of this device is demonstrated by fractionating the separation of a tryptic digest of a known protein mixture onto the microarray chip and subsequently analyzing the sample archive using matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS). Resulting peak widths are found to be significantly reduced compared to standard continuous flow spotting technologies as well as in comparison to a conventional nano-LC-electrospray ionization-mass spectrometry interface. Moreover, we demonstrate the advantage of our high-definition nanofractionation device by applying two different MALDI matrices to all collected fractions in an alternating fashion. Since the information that is obtained from a MALDI-MS measurement depends on the choice of MALDI matrix, we can extract complementary information from neighboring spots containing almost identical composition but different matrices.

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