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Publication : Peroxidasin-mediated bromine enrichment of basement membranes.

First Author  He C Year  2020
Journal  Proc Natl Acad Sci U S A Volume  117
Issue  27 Pages  15827-15836
PubMed ID  32571911 Mgi Jnum  J:291034
Mgi Id  MGI:6444560 Doi  10.1073/pnas.2007749117
Citation  He C, et al. (2020) Peroxidasin-mediated bromine enrichment of basement membranes. Proc Natl Acad Sci U S A 117(27):15827-15836
abstractText  Bromine and peroxidasin (an extracellular peroxidase) are essential for generating sulfilimine cross-links between a methionine and a hydroxylysine within collagen IV, a basement membrane protein. The sulfilimine cross-links increase the structural integrity of basement membranes. The formation of sulfilimine cross-links depends on the ability of peroxidasin to use bromide and hydrogen peroxide substrates to produce hypobromous acid (HOBr). Once a sulfilimine cross-link is created, bromide is released into the extracellular space and becomes available for reutilization. Whether the HOBr generated by peroxidasin is used very selectively for creating sulfilimine cross-links or whether it also causes oxidative damage to bystander molecules (e.g., generating bromotyrosine residues in basement membrane proteins) is unclear. To examine this issue, we used nanoscale secondary ion mass spectrometry (NanoSIMS) imaging to define the distribution of bromine in mammalian tissues. We observed striking enrichment of bromine ((79)Br, (81)Br) in basement membranes of normal human and mouse kidneys. In peroxidasin knockout mice, bromine enrichment of basement membranes of kidneys was reduced by approximately 85%. Proteomic studies revealed bromination of tyrosine-1485 in the NC1 domain of alpha2 collagen IV from kidneys of wild-type mice; the same tyrosine was brominated in collagen IV from human kidney. Bromination of tyrosine-1485 was reduced by >90% in kidneys of peroxidasin knockout mice. Thus, in addition to promoting sulfilimine cross-links in collagen IV, peroxidasin can also brominate a bystander tyrosine. Also, the fact that bromine enrichment is largely confined to basement membranes implies that peroxidasin activity is largely restricted to basement membranes in mammalian tissues.
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