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. 1998 Nov;54(11):1203–1216. doi: 10.1007/s000180050248

The structure of human interferon-β: implications for activity

M Karpusas 1, A Whitty 1, L Runkel 1, P Hochman 1
PMCID: PMC11147404  PMID: 9849615

Abstract.

Interferons (IFNs) are potent extracellular protein mediators of host defence and homoeostasis. This article reviews the structure of human IFN-β (HuIFN-β), in particular in relation to its activity. The recently determined crystal structure of HuIFN-β provides a framework for understanding of the mechanism of differentiation of type I IFNs by their common receptor. Insights are generated by comparison with the structures of other type I IFNs and from the interpretation of existing mutagenesis data. The details of the observed carbohydrate structure, together with biochemical data, implicate the glycosylation of HuIFN-β, which is uncommon among type I IFNs, as an important factor in the solubility, stability and, consequently, activity of the protein. Finally, these structural implications are discussed in the context of the clinical use of HuIFN-β.

Keywords: Key words. Interferon; crystal structure; cytokine; aggregation; glycosylation; multiple sclerosis.

Footnotes

Received 12 June 1998; received after revision 16 July 1998; accepted 16 July 1998


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