研究業績

主な原著論文

• “Novel Methods for Inhibiting Amyloidogenesis in the Presence of Peptides to Block Hydrophobic Interactions”
  Masatoshi Saiki, Ikumi Shibatate
  Journal of Peptides, 1, 27-33 (2024).
• “Irradiation effect of a submillimeter wave from 420 GHz gyrotron on amyloid peptides in vitro”
  Takayasu Kawasaki, Yuusuke Yamaguchi, Tomomi Ueda, Yuya Ishikawa, Toyonari Yaji, Toshiaki Ohta, Koichi Tsukiyama, Toshitaka Idehara, Masatoshi Saiki, and Masahiko Tani
  Biomed. Opt. Express, 11, 5341-5351 (2020).
• “The potential stem-forming sequence consists of the polymerization in Pmel17”
  Masatoshi Saiki , Ikumi Shibatate, and Takafumi Shizuma
  J Biorheol., 34, 24-29 (2020).
• “Structural stability of amyloid fibrils depends on the existence of the peripheral sequence near the core cross-β region”
  Masatoshi Saiki, Kohei Shiba, and Masaki Okumura
  FEBS Lett., 589, 3541-3547 (2015).
• “Evaluation of the structural stability of amyloid fibrils by dynamic light scattering” 
  Masatoshi Saiki and Mitsuhiro Akimoto 
  J Biorheol, 29, 24-27 (2015).
• “Radically Different Thioredoxin Domain Arrangement of ERp46, an Efficient Disulfide Bond Introducer of the Mammalian PDI Family”
  Rieko Kojima, Masaki Okumura, Shoji Masui, Shingo Kanemura, Michio Inoue, Masatoshi Saiki, Hiroshi Yamaguchi, Takaaki Hikima, Mamoru Suzuki, Shuji Akiyama, and Kenji Inaba
  Structure, 22, 431 (2014).
• “Synergistic cooperation of PDI family members in peroxiredoxin 4-driven oxidative protein folding” Yoshimi Sato, Rieko Kojima, Masaki Okumura, Masatoshi Hagiwara, Shoji Masui, Ken-ichi Maegawa, Masatoshi Saiki, Tomohisa Horibe, Mamoru Suzuki, Kenji Inaba
  Scientific Reports, 3, 2456 (2013). 
• “Stem-Forming Regions That Are Essential for the Amyloidogenesis of Prion Proteins” 
  Masatoshi Saiki, Yuji Hidaka, Masayuki Nara, and Hisayuki Morii 
  Biochemistry, 51, 1566–1576 (2012). 
• “Acceleration of disulfide-coupled protein folding using glutathione derivatives” 
  Masaki Okumura, Masatoshi Saiki, Hiroshi Yamaguchi, and Yuji Hidaka 
  FEBS Journal, 278, 1137-1144 (2011). 
• “Fiber formation of a synthetic spider peptide derived from Nephila clavata” 
  Yuji Hidaka, Ko-Ichi Kontani, Rina Taniguchi, Masatoshi Saiki, Sayoko Yokoi, Kenji Yukuhiro,
  Hiroshi Yamaguchi, and Mitsuhiro Miyazawa
  Biopolymers, 96, 222-227 (2011). 
• “Recognition of the N-Terminal Histone H2A and H3 Peptides by Peptidylarginine Deiminase IV”
  Masatoshi Saiki, Mayumi Watase, Hironori Matsubayashi, and Yuji Hidaka 
  Protein Pept. Lett., 16, 1012-1016 (2009).
• “Interaction-based evalution of the propensity for amyloid formation with cross-b structure”
  Masatoshi Saiki, Takeo Konakahara, and Hisayuki Morii 
  Biochem. Biophys. Res. Commun., 343, 1262-1271 (2006). 
• “Peripheral region for core cross-b plays important role in amyloidogenicity”
  Hisayuki Morii, Masatoshi Saiki, Takeo Konakahara, and Miyuki Ishimura 
  Biochem. Biophys. Res. Commun., 342, 808-816 (2006). 
• “Higher-order Molecular Packing in Amyloid-like Fibrils Constructed with Linear Arrangements of Hydrophobic and Hydrogen-bonding Side-chains” 
  Masatoshi Saiki, Shinya Honda, Kazunori Kawasaki, Deshan Zhou, Akira Kaito, Takeo Konakahara, and Hisayuki Morii 
  J. Mol. Biol., 348, 983-998 (2005). 

その他詳細の業績は こちら