Abstract
A new instrumental concept for extraction of nanovolumes from open microchannels (dimensions 150 μm × 50 μm, length 10 mm) manufactured on silicon microchips has been used in combination with a previously developed method for preconcentrating proteins and peptides in the open channels through electromigration. The extracted nanovolumes were further analyzed using nanoelectrospray ionization (nESI) or matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) directly or with subsequent enzymatic protein digestion in a nanodroplet prior to the MS analysis. Preconcentration of the samples resulted in a 15-fold sensitivity increase in nESI for a neurotensin solution, and using MALDI-MS, amyloid beta (Aβ) peptides could be detected in concentrations down to 1 nM. The method was also successfully applied for detection of cell culture Aβ.



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Acknowledgments
Patrik Ek is acknowledged for the help with the experimental setup and Thomas Frisk for the chip fabrication. Ute Haußmann, Hans-Wolfgang Klafki, and Jens Wiltfang are acknowledged for the Aβ cell culture sample and IP-protocol. The Swedish Research Council is acknowledged for financial support (grant no. 621-2009-4095).
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Mikkonen, S., Jacksén, J. & Emmer, Å. Mass spectrometric analysis of nanoscale sample volumes extracted from open microchannels after sample preconcentration applied on amyloid beta peptides. Anal Bioanal Chem 406, 3521–3524 (2014). https://doi.org/10.1007/s00216-014-7781-0
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DOI: https://doi.org/10.1007/s00216-014-7781-0


