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Lanekoff, I.

Publications and source records attributed to Lanekoff, I..

2 recordsLinked to original sources

PIA SSN: Parallel Image Acquisition and Spatial Similarity Network for Tandem Mass Spectrometry Imaging

Unambiguous molecular annotations are essential to discern complex local biochemical processes in spatial biology. Here we present a scalable and broadly applicable platform for tandem mass spectrometry imaging (MS2I) that overcomes current limitations in annotation with MSI by integrating Parallel Image Acquisition (PIA) with a novel open-access computational framework, Spatial Similarity Networking (SSN). The PIA employs parallelized acquisition of untargeted MSI and targeted MS2I data using multiple inclusion lists to ensure spatially consistent and structure-resolved imaging of hundreds of molecular species in a single experiment. For molecular annotation, we have developed the SSN that complements PIA by leveraging spatial correlations among product ions through a graph-based analysis framework to enable confident molecular annotation even within highly complex MS2I datasets. Using this integrated approach, we successfully resolved and annotated 134 phospholipid isomers and isobars from mouse brain tissue and suggest confidence levels for annotation for the MSI community. Furthermore, we applied our platform to interrogate cholesterol metabolism in human multiple sclerosis brain tissue, achieving annotation of six novel brain-related oxysterols and revealing spatially correlated oxidation pathways linked to lesion severity. Together, PIA and SSN establish a new framework for large-scale, structure-specific mass spectrometry imaging, with broad implications for spatial metabolomics, lipidomics, and chemical pathology beyond current capabilities.

neuroscience↗

Transcriptomic and functional mapping of autism associated environmental factors in developing human neurons

Research continues to identify genetic variation, environmental exposures, and their mixtures underlying different diseases and conditions. There is a need for screening methods to understand the molecular outcomes of such factors. Here, we investigate a highly efficient and multiplexable, fractional factorial experimental design (FFED) to study six environmental factors and four human induced pluripotent stem cell line derived differentiating human neural progenitors. We showcase the FFED coupled with RNA-sequencing to identify the effects of low-grade exposures to these environmental factors and analyse the results in the context of autism spectrum disorder (ASD). We performed this after five-day exposures on differentiating human neural progenitors accompanied by a layered analytical approach and detected several convergent and divergent, gene and pathway level responses. We revealed significant upregulation of pathways related to synaptic function and lipid metabolism following lead and fluoxetine exposure, respectively. The lipid changes were validated using mass spectrometry- based metabolomics after fluoxetine exposure. Our study demonstrates that the FFED can be used for multiplexed transcriptomic analyses to detect relevant pathway-level changes in human neural development caused by low-grade environmental risk factors. Future studies will require multiple cell lines with different genetic backgrounds for characterising the effects of environmental exposures in ASD.

neuroscience↗