{"database":"iProX","file_versions":[],"scores":null,"additional":{"omics_type":["Proteomics"],"submitter":["Xiaojun Xu"],"species":["Mus Musculus"],"full_dataset_link":["http://www.iprox.org/page/project.html?id=IPX0019907000"],"submitter_email":["xuxj26@mail2.sysu.edu.cn"],"submitter_affiliation":["The Eighth Affiliated Hospital, Sun Yat-Sen University"],"sample_protocol":[""],"repository":["iProX"],"data_protocol":[""],"additional_accession":[]},"is_claimable":false,"name":"HDAC1 K412 lactylation acts as an intrinsic metabolic barrier against p53-dependent osteoblast apoptosis in glucocorticoid-induced osteoporosis","description":"4D Label-free Lactylomics: Primary osteoblasts derived from Dex- or Dex/NaLa-treated mice were lysed in lysis buffer containing 8 M urea and protease/phosphatase inhibitors. After reduction and alkylation, proteins were digested with trypsin overnight. Peptides were incubated with pan-anti-lactyllysine antibody beads (PTM Biolabs, Cat# PTM-1401R) for enrichment. Enriched peptides were eluted, desalted, and analyzed using a Q Exactive HF-X mass spectrometer (Thermo Fisher Scientific) coupled to an Easy-nLC 1200 system. Raw data were searched against the Mus musculus UniProt database using MaxQuant software. A localization probability > 0.75 was used as the cutoff for modification site identification.","dates":{"publication":"Fri Sep 25 00:00:00 BST 2026"},"accession":"PXD084853","cross_references":{"TAXONOMY":["10090"]}}