Abstract
Mass spectrometry imaging (MSI) is a powerful
and convenient method for revealing the spatial chemical composition of
different biological samples. Molecular annotation of the detected signals is
only possible if a high mass accuracy is maintained over the entire image and
the m/z range. However, the heterogeneous molecular composition of biological
samples could lead to small fluctuations in the detected m/z-values, called
mass shift. The use of internal calibration is known to offer the best solution
to avoid, or at least to reduce, mass shifts. Their “a priori” selection for a
global MSI acquisition is prone to false positive detection and therefore to
poor recalibration. To fill this gap, this work describes an algorithm that
recalibrates each spectrum individually by estimating its mass shift with the
help of a list of pixel specific internal calibrating ions, automatically
generated in a data-adaptive manner
(https://github.com/LaRoccaRaphael/MSI_recalibration). Through a practical
example, we applied the methodology to a zebrafish whole body section acquired
at high mass resolution to demonstrate the impact of mass shift on data
analysis and the capability of our algorithm to recalibrate MSI data. In
addition, we illustrate the broad applicability of the method by recalibrating
31 different public MSI datasets from METASPACE from various samples and types
of MSI and show that our recalibration significantly increases the numbers of
METASPACE annotations (gaining from 20 up to 400 additional annotations),
particularly the high-confidence annotations with a low false discovery rate.