Proteome analysis of pulpal wound healing induced by S100A8-derived peptide and protein S100A8

Supplementary Tables for:
Novel Functional Peptide For Next-Generation Vital Pulp Therapy

M. Watanabe1, M. Okamoto1, S. Komichi1, H. Hailing1, S. Matsumoto1, K. Moriyama1, M. Ali2, T. Takebe3, I. Kozaki4, A, Fujimoto4, K. Kanie45, R. Kato4, K. Uto6, M. Ebara6, A. Ogata7, Y. Narita7, Y. Takahashi1, M. Hayashi1

1 Department of Restorative Dentistry and Endodontology, Osaka University Graduate School of Dentistry, Osaka, Japan
2 Department of Restorative Dentistry, Faculty of Dentistry, University of Khartoum, Khartoum, Sudan
3 Department of Oral and Maxillofacial Surgery, Osaka University Graduate School of Dentistry, Osaka, Japan
4 Department of Basic Medicinal Sciences, Graduate School of Pharmaceutical Sciences, Nagoya University, Aichi, Japan
5Department of Biotechnology and Chemistry, Kinki University, Hiroshima, Japan
6International Center for Materials Nanoarchitectonics (WPI-MANA), National Institute for Materials Science (NIMS), Ibaraki, Japan
7Department of Cardiac Surgery, Nagoya University Graduate School of Medicine , Aichi, Japan

To investigate the mechanism by which specific peptide promoted pulpal wound healing process, liquid chromatography-tandem mass spectrometry (LC-MS/MS) was performed to quantify the protein expression in human dental pulp stem cells (hDPSCs). Proteins identified by MS/MS were compared using Scaffold Viewer (Proteome Software).