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Secondary structures, dynamics, and DNA binding of the homeodomain of human SIX1.

Yan LiElizabeth YiHui NgYing Ru LohChong Yu GeaQiwei HuangQingxin LiCongBao Kang
Published in: Journal of peptide science : an official publication of the European Peptide Society (2021)
Human sine oculis homeobox homolog (SIX) 1 contains a homeodomain (HD), which is important for binding to DNA. In this study, we carried out structural studies on the HD of human SIX1 using nuclear magnetic resonance (NMR) spectroscopy. Its secondary structures and dynamics in solution were explored. HD is well-structured in solution, and our study shows that it contains three α-helices. Dynamics study indicates that the N- and C-terminal residues of HD are flexible in solution. HD of human SIX1 exhibits molecular interactions with a short double-strand DNA sequence evidenced by the 1 H-15 N-heteronuclear single quantum correlation (HSQC) and 19 F-NMR experiments. Our current study provides structural information for HD of human SIX1. Further studies indicate that this construct can be utilized to study SIX1 and DNA interactions.
Keyphrases
  • endothelial cells
  • magnetic resonance
  • induced pluripotent stem cells
  • high resolution
  • transcription factor
  • single molecule
  • pluripotent stem cells
  • circulating tumor
  • mass spectrometry
  • amino acid
  • health information