Functionality of Intrinsic Disorder in Tumor Necrosis Factor-α and Its Receptors

Document Type

Article

Publication Date

2017

Keywords

cytokine, intrinsic disorder, intrinsically disordered protein, post-translational modifications, protein–protein interactions, tumor necrosis factor-α

Digital Object Identifier (DOI)

https://doi.org/10.1111/febs.14182

Abstract

Tumor necrosis factor-α (TNF-α) is a pleiotropic inflammatory cytokine that exerts potent cytotoxic effects on solid tumor cells, while not affecting their normal counterparts. It is also known that TNF-α exerts many of its biological functions via interaction with specific receptors. To understand the potential roles of intrinsic disorder in the functioning of this important cytokine, we explored the peculiarities of intrinsic disorder distribution in human TNF-α and its homologs from various species, ranging from zebrafish to chimpanzee. We also studied the peculiarities of intrinsic disorder distribution in human TNF-α receptors, TNFR1 and TNFR2. Analysis revealed that cytoplasmic domains of TNF-α and its receptors are expected to be highly disordered. Furthermore, although the sequence identities of analyzed TNF-α homologs range from 99.57% (between human and chimpanzee proteins) to 22.33% (between frog and fish proteins), their intrinsic disorder profiles are characterized by a remarkable similarity. These observations indicate that the peculiarities of distribution of the intrinsic disorder propensity within the amino acid sequences are evolutionary conserved, and therefore could be of functional importance for this family of proteins. We also show that disordered and flexible regions of human TNF-α and its TNFR1 and TNFR2 receptors are crucial for some of their biological activities.

Was this content written or created while at USF?

Yes

Citation / Publisher Attribution

The FEBS Journal, v. 284, issue 21, p. 3589-3618

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