Two serine residues distinctly regulate the rescue function of Humanin, an inhibiting factor of Alzheimer's disease-related neurotoxicity

Functional potentiation by isomerization and dimerization

Kenzo Terashita, Yuichi Hashimoto, Takako Niikura, Hirohisa Tajima, Yohichi Yamagishi, Miho Ishizaka, Masaoki Kawasumi, Tomohiro Chiba, Kohsuke Kanekura, Marina Yamada, Mikiro Nawa, Yoshiko Kita, Sadakazu Aiso, Ikuo Nishimoto

Research output: Contribution to journalArticle

54 Citations (Scopus)

Abstract

The 24-residue peptide Humanin (HN), containing two Ser residues at positions 7 and 14, protects neuronal cells from insults of various Alzheimer's disease (AD) genes and Aβ. It was not known why the rescue function of (S14G)HN is more potent than HN by two to three orders of magnitude. Investigating the possibility that the post-translational modification of Ser14 might play a role, we found that HN with D-Ser at position 14 exerts neuroprotection more potently than HN by two to three orders of magnitude, whereas D-Ser7 substitution does not affect the rescue function of HN. On the other hand, S7A substitution nullified the HN function. Multiple series of experiments indicated that Ser7 is necessary for self-dimerization of HN, which is essential for neuroprotection by this factor. These findings indicate that the rescue function of HN is quantitatively modulated by D-isomerization of Ser14 and Ser7-relevant dimerization, allowing for the construction of a very potent HN derivative that was fully neuroprotective at 10 pM against 25 μM Aβ1-43. This study provides important clues to the understanding of the neuroprotective mechanism of HN, as well as to the development of novel AD therapeutics.

Original languageEnglish
Pages (from-to)1521-1538
Number of pages18
JournalJournal of Neurochemistry
Volume85
Issue number6
DOIs
Publication statusPublished - 2003 Jun 1
Externally publishedYes

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Dimerization
Isomerization
Serine
Substitution reactions
humanin
Genes
Derivatives
Peptides

Keywords

  • Alzheimer's disease
  • D-serine isomerization
  • Dimerization
  • Humanin
  • Neuronal death
  • Neuroprotection

ASJC Scopus subject areas

  • Biochemistry
  • Cellular and Molecular Neuroscience

Cite this

Two serine residues distinctly regulate the rescue function of Humanin, an inhibiting factor of Alzheimer's disease-related neurotoxicity : Functional potentiation by isomerization and dimerization. / Terashita, Kenzo; Hashimoto, Yuichi; Niikura, Takako; Tajima, Hirohisa; Yamagishi, Yohichi; Ishizaka, Miho; Kawasumi, Masaoki; Chiba, Tomohiro; Kanekura, Kohsuke; Yamada, Marina; Nawa, Mikiro; Kita, Yoshiko; Aiso, Sadakazu; Nishimoto, Ikuo.

In: Journal of Neurochemistry, Vol. 85, No. 6, 01.06.2003, p. 1521-1538.

Research output: Contribution to journalArticle

Terashita, K, Hashimoto, Y, Niikura, T, Tajima, H, Yamagishi, Y, Ishizaka, M, Kawasumi, M, Chiba, T, Kanekura, K, Yamada, M, Nawa, M, Kita, Y, Aiso, S & Nishimoto, I 2003, 'Two serine residues distinctly regulate the rescue function of Humanin, an inhibiting factor of Alzheimer's disease-related neurotoxicity: Functional potentiation by isomerization and dimerization', Journal of Neurochemistry, vol. 85, no. 6, pp. 1521-1538. https://doi.org/10.1046/j.1471-4159.2003.01797.x
Terashita, Kenzo ; Hashimoto, Yuichi ; Niikura, Takako ; Tajima, Hirohisa ; Yamagishi, Yohichi ; Ishizaka, Miho ; Kawasumi, Masaoki ; Chiba, Tomohiro ; Kanekura, Kohsuke ; Yamada, Marina ; Nawa, Mikiro ; Kita, Yoshiko ; Aiso, Sadakazu ; Nishimoto, Ikuo. / Two serine residues distinctly regulate the rescue function of Humanin, an inhibiting factor of Alzheimer's disease-related neurotoxicity : Functional potentiation by isomerization and dimerization. In: Journal of Neurochemistry. 2003 ; Vol. 85, No. 6. pp. 1521-1538.
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T2 - Functional potentiation by isomerization and dimerization

AU - Terashita, Kenzo

AU - Hashimoto, Yuichi

AU - Niikura, Takako

AU - Tajima, Hirohisa

AU - Yamagishi, Yohichi

AU - Ishizaka, Miho

AU - Kawasumi, Masaoki

AU - Chiba, Tomohiro

AU - Kanekura, Kohsuke

AU - Yamada, Marina

AU - Nawa, Mikiro

AU - Kita, Yoshiko

AU - Aiso, Sadakazu

AU - Nishimoto, Ikuo

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