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Mitochondrial Targeting Domain Homologs Induce Necrotic Cell Death Via Mitochondrial and Endoplasmic Reticulum Disruption.
Park, Junghee; Han, Ji-Hye; Myung, Seung-Hyun; Chung, Hea-Jong; Park, Jae-Il; Cho, Ju-Yeon; Kim, Tae-Hyoung.
Afiliação
  • Park J; Department of Biochemistry and Molecular Biology, Chosun University School of Medicine, Gwangju 61452, Republic of Korea.
  • Han JH; Department of Biochemistry and Molecular Biology, Chosun University School of Medicine, Gwangju 61452, Republic of Korea.
  • Myung SH; Department of Biochemistry and Molecular Biology, Chosun University School of Medicine, Gwangju 61452, Republic of Korea.
  • Chung HJ; Gwangju Center, Korea Basic Science Institute, Gwangju 61168, Republic of Korea.
  • Park JI; Gwangju Center, Korea Basic Science Institute, Gwangju 61168, Republic of Korea.
  • Cho JY; Department of Medicine, Chosun University Hospital, Gwangju 61453, Republic of Korea.
  • Kim TH; Department of Biochemistry and Molecular Biology, Chosun University School of Medicine, Gwangju 61452, Republic of Korea.
J Microbiol Biotechnol ; 31(6): 875-881, 2021 Jun 28.
Article em En | MEDLINE | ID: mdl-34024890
ABSTRACT
The mitochondrial targeting domain (MTD) of Noxa contributes to its mitochondrial localization and to apoptosis induction. As a peptide, MTD fused with octa-arginine (R8), a CPP, induces necrosis related to intracellular calcium influx and destruction of mitochondria and endoplasmic reticulum. We searched for homologs of MTD, and compared their cell killing capability when fused with R8. Three of the seven peptides triggered cell death with similar mechanisms. The comparative analysis of peptide sequences showed that four amino acid sites of MTD are critical in regulating necrosis, suggesting the potential to generate artificial, adjustable cytotoxic peptides, which could be effective medicines for many diseases. Thus, homologs functionality could hint to the functions of their belonging proteins.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Morte Celular / Retículo Endoplasmático / Proteínas Reguladoras de Apoptose / Mitocôndrias Limite: Humans Idioma: En Revista: J Microbiol Biotechnol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Morte Celular / Retículo Endoplasmático / Proteínas Reguladoras de Apoptose / Mitocôndrias Limite: Humans Idioma: En Revista: J Microbiol Biotechnol Ano de publicação: 2021 Tipo de documento: Article