<HashMap><database>biostudies-literature</database><scores/><additional><submitter>van der Spek SJF</submitter><funding>ZonMw</funding><pagination>1588</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8304546</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>10(7)</volume><pubmed_abstract>Alzheimer's disease (AD) is the most common neurodegenerative disorder in the human population, for which there is currently no cure. The cause of AD is unknown; however, the toxic effects of amyloid-β (Aβ) are believed to play a role in its onset. To investigate this, we examined changes in global protein levels in a hippocampal synaptosome fraction of the Amyloid Precursor Protein swe/Presenelin 1 dE9 (APP/PS1) mouse model of AD at 6 and 12 months of age (moa). Data independent acquisition (DIA), or Sequential Window Acquisition of all THeoretical fragment-ion (SWATH), was used for a quantitative label-free proteomics analysis. We first assessed the usefulness of a recently improved directDIA workflow as an alternative to conventional DIA data analysis using a project-specific spectral l</pubmed_abstract><journal>Cells</journal><pubmed_title>Age-Dependent Hippocampal Proteomics in the APP/PS1 Alzheimer Mouse Model: A Comparative Analysis with Classical SWATH/DIA and directDIA Approaches.</pubmed_title><pmcid>PMC8304546</pmcid><funding_grant_id>733051076</funding_grant_id><funding_grant_id>733050811</funding_grant_id><funding_grant_id>733050106</funding_grant_id><pubmed_authors>Li KW</pubmed_authors><pubmed_authors>Miedema SSM</pubmed_authors><pubmed_authors>Paliukhovich I</pubmed_authors><pubmed_authors>Koopmans F</pubmed_authors><pubmed_authors>van der Spek SJF</pubmed_authors><pubmed_authors>Gonzalez-Lozano MA</pubmed_authors><pubmed_authors>Smit AB</pubmed_authors></additional><is_claimable>false</is_claimable><name>Age-Dependent Hippocampal Proteomics in the APP/PS1 Alzheimer Mouse Model: A Comparative Analysis with Classical SWATH/DIA and directDIA Approaches.</name><description>Alzheimer's disease (AD) is the most common neurodegenerative disorder in the human population, for which there is currently no cure. The cause of AD is unknown; however, the toxic effects of amyloid-β (Aβ) are believed to play a role in its onset. To investigate this, we examined changes in global protein levels in a hippocampal synaptosome fraction of the Amyloid Precursor Protein swe/Presenelin 1 dE9 (APP/PS1) mouse model of AD at 6 and 12 months of age (moa). Data independent acquisition (DIA), or Sequential Window Acquisition of all THeoretical fragment-ion (SWATH), was used for a quantitative label-free proteomics analysis. We first assessed the usefulness of a recently improved directDIA workflow as an alternative to conventional DIA data analysis using a project-specific spectral l</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Jun</publication><modification>2026-04-08T08:58:11.352Z</modification><creation>2022-02-10T23:39:03.24Z</creation></dates><accession>S-EPMC8304546</accession><cross_references><pubmed>34202490</pubmed><doi>10.3390/cells10071588</doi></cross_references></HashMap>