<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Alaiya A</submitter><funding>King Abdullah International Medical Research Center</funding><pagination>6787</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11204259</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>25(12)</volume><pubmed_abstract>Heat stroke, a hazardous hyperthermia-related illness, is characterized by CNS injury, particularly long-lasting brain damage. A root cause for hyperthermic neurological damage is heat-induced proteotoxic stress through protein aggregation, a known causative agent of neurological disorders. Stress magnitude and enduring persistence are highly correlated with hyperthermia-associated neurological damage. We used an untargeted proteomic approach using liquid chromatography-tandem mass spectrometry (LC-MS/MS) to identify and characterize time-series proteome-wide changes in dose-responsive proteotoxic stress models in medulloblastoma [Daoy], neuroblastoma [SH-SY5Y], and differentiated SH-SY5Y neuron-like cells [SH(D)]. An integrated analysis of condition-time datasets identified global proteom</pubmed_abstract><journal>International journal of molecular sciences</journal><pubmed_title>Proteomics Analysis of Proteotoxic Stress Response in In-Vitro Human Neuronal Models.</pubmed_title><pmcid>PMC11204259</pmcid><funding_grant_id>RC16/196</funding_grant_id><pubmed_authors>Albinhassan TH</pubmed_authors><pubmed_authors>Bouchama A</pubmed_authors><pubmed_authors>Mohammad S</pubmed_authors><pubmed_authors>Shinwari Z</pubmed_authors><pubmed_authors>Rashid M</pubmed_authors><pubmed_authors>Alwesmi MB</pubmed_authors><pubmed_authors>Malik SS</pubmed_authors><pubmed_authors>Alharbi BM</pubmed_authors><pubmed_authors>Alaiya A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Proteomics Analysis of Proteotoxic Stress Response in In-Vitro Human Neuronal Models.</name><description>Heat stroke, a hazardous hyperthermia-related illness, is characterized by CNS injury, particularly long-lasting brain damage. A root cause for hyperthermic neurological damage is heat-induced proteotoxic stress through protein aggregation, a known causative agent of neurological disorders. Stress magnitude and enduring persistence are highly correlated with hyperthermia-associated neurological damage. We used an untargeted proteomic approach using liquid chromatography-tandem mass spectrometry (LC-MS/MS) to identify and characterize time-series proteome-wide changes in dose-responsive proteotoxic stress models in medulloblastoma [Daoy], neuroblastoma [SH-SY5Y], and differentiated SH-SY5Y neuron-like cells [SH(D)]. An integrated analysis of condition-time datasets identified global proteom</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jun</publication><modification>2026-04-07T22:56:10.432Z</modification><creation>2026-04-07T18:48:11.008Z</creation></dates><accession>S-EPMC11204259</accession><cross_references><pubmed>38928492</pubmed><doi>10.3390/ijms25126787</doi></cross_references></HashMap>