posted on 2013-10-15, 00:00authored byMartin Pabst, Stephan R. Fagerer, Rudolf Köhling, Simon K. Küster, Robert Steinhoff, Martin Badertscher, Fabian Wahl, Petra S. Dittrich, Konstantins Jefimovs, Renato Zenobi
Matrix-assisted laser desorption/ionization
mass spectrometry (MALDI-MS)
is a fast analysis tool employed for the detection of a broad range
of analytes. However, MALDI-MS has a reputation of not being suitable
for quantitative analysis. Inhomogeneous analyte/matrix co-crystallization,
spot-to-spot inhomogeneity, as well as a typically low number of replicates
are the main contributing factors. Here, we present a novel MALDI
sample target for quantitative MALDI-MS applications, which addresses
the limitations mentioned above. The platform is based on the recently
developed microarray for mass spectrometry (MAMS) technology and contains
parallel lanes of hydrophilic reservoirs. Samples are not pipetted
manually but deposited by dragging one or several sample droplets
with a metal sliding device along these lanes. Sample is rapidly and
automatically aliquoted into the sample spots due to the interplay
of hydrophilic/hydrophobic interactions. With a few microliters of
sample, it is possible to aliquot up to 40 replicates within seconds,
each aliquot containing just 10 nL. The analyte droplet dries immediately
and homogeneously, and consumption of the whole spot during MALDI-MS
analysis is typically accomplished within few seconds. We evaluated
these sample targets with respect to their suitability for use with
different samples and matrices. Furthermore, we tested their application
for generating calibration curves of standard peptides with α-cyano-4-hdydroxycinnamic
acid as a matrix. For angiotensin II and [Glu1]-fibrinopeptide
B we achieved coefficients of determination (r2) greater than 0.99 without the use of internal standards.