<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Toribio D</submitter><funding>NEI NIH HHS</funding><pagination>44</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12013672</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>66(4)</volume><pubmed_abstract>&lt;h4>Purpose&lt;/h4>The lacrimal gland (LG) is the major source of aqueous tears, and insufficient LG secretion leads to aqueous-deficient dry eye (ADDE) disease. To provide a foundational description of LG's protein expression patterns, we prepared protein extracts of LGs from a wild-type and an ADDE mouse model and analyzed the proteome by quantitative mass spectrometry.&lt;h4>Methods&lt;/h4>LGs were isolated from an ADDE mouse model, male non-obese diabetic (NOD) mice and control wild-type BALB/c mice (n = 6 each). Protein samples were prepared in urea-based lysis buffer and protein concentrations determined by the BCA method. The equivalent of 200 µg protein were tryptically digested and analyzed by nanoflow liquid chromatography tandem mass spectrometry (LC-MS/MS). Proteins were identified and </pubmed_abstract><journal>Investigative ophthalmology &amp; visual science</journal><pubmed_title>Quantitative Changes in the Proteome of Chronically Inflamed Lacrimal Glands From a Sjogren's Disease Animal Model.</pubmed_title><pmcid>PMC12013672</pmcid><funding_grant_id>R01 EY029870</funding_grant_id><pubmed_authors>Morokuma J</pubmed_authors><pubmed_authors>Pellino D</pubmed_authors><pubmed_authors>Zoukhri D</pubmed_authors><pubmed_authors>Toribio D</pubmed_authors><pubmed_authors>Hardt M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Quantitative Changes in the Proteome of Chronically Inflamed Lacrimal Glands From a Sjogren's Disease Animal Model.</name><description>&lt;h4>Purpose&lt;/h4>The lacrimal gland (LG) is the major source of aqueous tears, and insufficient LG secretion leads to aqueous-deficient dry eye (ADDE) disease. To provide a foundational description of LG's protein expression patterns, we prepared protein extracts of LGs from a wild-type and an ADDE mouse model and analyzed the proteome by quantitative mass spectrometry.&lt;h4>Methods&lt;/h4>LGs were isolated from an ADDE mouse model, male non-obese diabetic (NOD) mice and control wild-type BALB/c mice (n = 6 each). Protein samples were prepared in urea-based lysis buffer and protein concentrations determined by the BCA method. The equivalent of 200 µg protein were tryptically digested and analyzed by nanoflow liquid chromatography tandem mass spectrometry (LC-MS/MS). Proteins were identified and </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Apr</publication><modification>2026-06-03T01:27:26.674Z</modification><creation>2025-07-03T03:04:55.201Z</creation></dates><accession>S-EPMC12013672</accession><cross_references><pubmed>40244610</pubmed><doi>10.1167/iovs.66.4.44</doi></cross_references></HashMap>