TY - JOUR
T1 - The basic helix-loop-helix region of the transcriptional repressor hairy and enhancer of split 1 is preorganized to bind DNA
AU - Popovic, Matija
AU - Wienk, Hans
AU - Coglievina, Maristella
AU - Boelens, Rolf
AU - Pongor, Sándor
AU - Pintar, Alessandro
PY - 2014/1/1
Y1 - 2014/1/1
N2 - Hairy and enhancer of split 1, one of the main downstream effectors in Notch signaling, is a transcriptional repressor of the basic helix-loop-helix (bHLH) family. Using nuclear magnetic resonance methods, we have determined the structure and dynamics of a recombinant protein, H1H, which includes an N-terminal segment, b1, containing functionally important phosphorylation sites, the basic region b2, required for binding to DNA, and the HLH domain. We show that a proline residue in the sequence divides the protein in two parts, a flexible and disordered N-terminal region including b1 and a structured, mainly helical region comprising b2 and the HLH domain. Binding of H1H to a double strand DNA oligonucleotide was monitored through the chemical shift perturbation of backbone amide resonances, and showed that the interaction surface involves not only the b2 segment but also several residues in the b1 and HLH regions.
AB - Hairy and enhancer of split 1, one of the main downstream effectors in Notch signaling, is a transcriptional repressor of the basic helix-loop-helix (bHLH) family. Using nuclear magnetic resonance methods, we have determined the structure and dynamics of a recombinant protein, H1H, which includes an N-terminal segment, b1, containing functionally important phosphorylation sites, the basic region b2, required for binding to DNA, and the HLH domain. We show that a proline residue in the sequence divides the protein in two parts, a flexible and disordered N-terminal region including b1 and a structured, mainly helical region comprising b2 and the HLH domain. Binding of H1H to a double strand DNA oligonucleotide was monitored through the chemical shift perturbation of backbone amide resonances, and showed that the interaction surface involves not only the b2 segment but also several residues in the b1 and HLH regions.
KW - Backbone dynamics
KW - Chemical shift perturbation
KW - Conformational selection
KW - NMR
KW - Secondary structure
UR - http://www.scopus.com/inward/record.url?scp=84895529675&partnerID=8YFLogxK
U2 - 10.1002/prot.24507
DO - 10.1002/prot.24507
M3 - Article
C2 - 24403087
AN - SCOPUS:84895529675
SN - 0887-3585
VL - 82
SP - 537
EP - 545
JO - Proteins: Structure function and bioinformatics
JF - Proteins: Structure function and bioinformatics
IS - 4
ER -