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The Binding of Factor H to a Complex of Physiological Polyanions and C3b on Cells is Impaired in Atypical Hemolytic Uremic Syndrome
Factor H (fH) is essential for complement homeostasis in fluid-phase and on surfaces. Its two C-terminal domains (CCP 19-20) anchor fH to self surfaces where it prevents C3b amplification in a process requiring its N-terminal four domains. In atypical hemolytic uremic syndrome (aHUS), mutations clus...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2696619/ https://ncbi.nlm.nih.gov/pubmed/19454698 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4049/jimmunol.0804031 |
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