PLoS ONE · 2015 · 38 citations · 62 references
Life SciencesBiochemistryMolecular BiologyCell SignalingSignal TransductionStructural BiologyCell Signaling NetworksIntrinsic DisorderIntrinsically Disordered ProteinsProtein MisfoldingProtein Misfolding DisordersProtein StructureDisorder In Signaling ProteinsDisorder In Transcriptional RegulationDisordered ProteinsIntrinsic Disorder AnalysisIntrinsic Disorder PropensityProtein Conformational DisordersProtein Disorder PropensityStructure-function Relationships In Disordered Proteins
Intrinsically disordered proteins (IDPs) are abundant in complex organisms. Due to their promiscuous nature and their ability to adopt several conformations IDPs constitute important points of network regulation. The family of Brain Expressed and X-linked (Bex) proteins consists of 5 members in humans (Bex1-5). Recent reports have implicated Bex proteins in transcriptional regulation and signaling pathways involved in neurodegeneration, cancer, cell cycle and tumor growth. However, structural and biophysical data for this protein family is almost non-existent. We used bioinformatics analyses to show that Bex proteins contain long regions of intrinsic disorder which are conserved across all members. Moreover, we confirmed the intrinsic disorder by circular dichroism spectroscopy of Bex1 after expression and purification in E. coli. These observations strongly suggest that Bex proteins constitute a new group of IDPs. Based on these findings, together with the demonstrated promiscuity of Bex proteins and their involvement in different signaling pathways, we propose that Bex family members play important roles in the formation of protein network hubs.
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