Accéder directement au contenu Accéder directement à la navigation
Article dans une revue

Fragment-Based NMR Study of the Conformational Dynamics in the bHLH Transcription Factor Ascl1.

Abstract : The Achaete-scute homolog 1 (Ascl1) protein regulates a large subset of genes that leads neuronal progenitor cells to distinctive differentiation pathways during human brain development. Although it is well known that Ascl1 binds DNA as a homo- or heterodimer via its basic helix-loop-helix (bHLH) motif, little is known about the conformational sampling properties of the DNA-free full-length protein, and in particular about the bHLH domain-flanking N- and C-terminal segments, which are predicted to be highly disordered in solution. The structural heterogeneity, low solubility, and high aggregation propensity of Ascl1 in aqueous buffer solutions make high-resolution studies of this protein a challenging task. Here, we have adopted a fragment-based strategy that allowed us to obtain high-quality NMR data providing, to our knowledge, the first comprehensive high-resolution information on the structural propensities and conformational dynamics of Ascl1. The emerging picture is that of an overall extended and highly dynamic polypeptide chain comprising three helical segments and lacking persistent long-range interactions. We also show that the C-terminal helix of the bHLH domain is involved in intermolecular interactions, even in the absence of DNA. Our results contribute to a better understanding of the mechanisms of action that govern the regulation of proneural transcription factors.
Type de document :
Article dans une revue
Liste complète des métadonnées
Contributeur : Frank Thomas <>
Soumis le : jeudi 18 mai 2017 - 10:41:05
Dernière modification le : mercredi 14 octobre 2020 - 04:17:18

Lien texte intégral




Lorenzo Baronti, Tomáš Hošek, Sergio Gil-Caballero, Hadas Raveh-Amit, Eduardo O Calçada, et al.. Fragment-Based NMR Study of the Conformational Dynamics in the bHLH Transcription Factor Ascl1.. Biophysical Journal, Biophysical Society, 2017, 112 (7), pp.1366-1373. ⟨10.1016/j.bpj.2017.02.025⟩. ⟨hal-01524439⟩



Consultations de la notice