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Identification of HAO2 Protein-Protein Interactions by Mass Spectrometry

ABSTRACT: This project focuses on the systematic identification and characterization of proteins that interact with HAO2 (Hydroxyacid Oxidase 2) using advanced mass spectrometry techniques. The primary goal is to map the HAO2 interactome to gain insights into its biological functions, regulatory mechanisms, and potential role in metabolic pathways or disease states. By isolating HAO2-containing protein complexes and analyzing them via high-resolution mass spectrometry, we aim to generate a reliable list of binding partners. Subsequent bioinformatic analysis will help elucidate the involved cellular processes and networks. This research is fundamental for understanding the protein's physiological context and could reveal novel targets for further functional validation or therapeutic intervention.

ORGANISM(S): Homo Sapiens

SUBMITTER: Jing Ye

PROVIDER: PXD075174 | iProX | Tue Mar 03 00:00:00 GMT 2026

REPOSITORIES: iProX

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Project description:The goal of this project is to understand the etiology and pathology of host-pathogen interaction using high-throughput cellular phenotyping. By combining the expertise in pathogen biology, informatics and stem cell biology across the institute, this project will use targeted genetic modification in mouse embryonic stem cells to identify functions of host genes in innate immunity. We will also explore the biology of mouse embryonic stem cells and their differentiation into immune competent cells. To this end we will generate homozygous and inducible knockout lines in mouse embryonic stem cells, which will be differentiated into immune competent cells, such as macrophages or dendritic cells. These will be subjected to a panel of immune challenge and stimulation assays to characterise the functions of the disrupted genes. To identify new functions for mammalian genes in innate immunity we will:\Generate a panel of homozygous inducible gene knockout mouse ES cell lines working from a list of ca. 80 candidate genes (MGP phenotyping and GWAS hits). \Scale up differentiation protocols for immune challenge and stimulation assays.\Benchmark in vitro differentiated ES cell models against primary immune cells from selected MGP mouse lines and eventually against human iPS cells.\Screen a panel of 30 genetically modified cell lines in immunological challenge and stimulation assays, defining phenotypes at the cellular level by high content imaging, biochemically by assaying cytokine production, and at the molecular level by transcriptome analysis.\Define novel gene functions in innate immunity through network analysis of gene expression data from all challenged cell lines.\In the longer term scale up the production and phenotyping of genetically modified cell lines (mouse or human as appropriate).This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/

Dataset Information

Identification of HAO2 Protein-Protein Interactions by Mass Spectrometry

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