Dataset DZNE-2025-00818

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Dataset: Plasma proteomics of BACE2 KO mice

 ;

2024
PRoteomics IDEntifications Database

PRoteomics IDEntifications Database ()

Abstract: The beta-secretase BACE1 is a central drug target for Alzheimer’s disease. Clinically tested, BACE1-directed inhibitors also block the homologous protease BACE2. Yet, little is known about physiological BACE2 substrates and functions in vivo. Here, we performed discovery proteomics to identify substrates of the protease BACE2 in plasma of mice. Therefore, we analysed plasma from BACE2 KO, and WT controls. Inactivation of BACE2 inhibited shedding of VEGFR3/FLT4. Thus, sVEGFR3 represents a pharmacodynamic plasma marker for BACE2 activity in vivo.


Contributing Institute(s):
  1. Neuroproteomics (AG Lichtenthaler)
Research Program(s):
  1. 352 - Disease Mechanisms (POF4-352) (POF4-352)

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The record appears in these collections:
Document types > Other Resources > Datasets
Institute Collections > M DZNE > M DZNE-AG Lichtenthaler
Public records
Publications Database


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The Alzheimer's disease-linked protease BACE2 cleaves VEGFR3 and modulates its signaling.
The journal of clinical investigation 134(16), e170550 () [10.1172/JCI170550] OpenAccess  Download fulltext Files  Download fulltextFulltext by Pubmed Central BibTeX | EndNote: XML, Text | RIS


 Record created 2025-07-08, last modified 2025-07-09


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