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dc.contributor.authorTerada, Kayoen
dc.contributor.authorGimenez-Dejoz, Joanen
dc.contributor.authorKurita, Taichien
dc.contributor.authorOikawa, Kazusatoen
dc.contributor.authorUji, Hirotakaen
dc.contributor.authorTsuchiya, Kousukeen
dc.contributor.authorNumata, Keijien
dc.contributor.alternative寺田, 佳世ja
dc.contributor.alternative栗田, 太一ja
dc.contributor.alternative及川, 和聡ja
dc.contributor.alternative宇治, 広隆ja
dc.contributor.alternative土屋, 康佑ja
dc.contributor.alternative沼田, 圭司ja
dc.date.accessioned2022-10-03T07:44:49Z-
dc.date.available2022-10-03T07:44:49Z-
dc.date.issued2021-04-12-
dc.identifier.urihttp://hdl.handle.net/2433/276532-
dc.description.abstractIn the genetic modification of plant cells, the mitochondrion is an important target in addition to the nucleus and plastid. However, gene delivery into the mitochondria of plant cells has yet to be established by conventional methods, such as particle bombardment, because of the small size and high mobility of mitochondria. To develop an efficient mitochondria-targeting signal (MTS) that functions in plant cells, we designed the artificial peptide (LURL)₃ and its analogues, which periodically feature hydrophobic α-aminoisobutyric acid (Aib, U) and cationic arginine (R), considering the consensus motif recognized by the mitochondrial import receptor Tom20. Circular dichroism measurements and molecular dynamics simulation studies revealed that (LURL)₃ had a propensity to form a stable α-helix in 0.1 M phosphate buffer solution containing 1.0 wt % sodium dodecyl sulfate. After internalization into plant cells via particle bombardment, (LURL)₃ revealed highly selective accumulation in the mitochondria, whereas its analogue (LARL)₃ was predominantly located in the vacuoles in addition to mitochondria. The high selectivity of (LURL)₃ can be attributed to the incorporation of Aib, which promotes the hydrophobic interaction between the MTS and Tom20 by increasing the hydrophobicity and helicity of (LURL)₃. The present study provided a prospective mitochondrial targeting system using the simple design of artificial peptides.en
dc.language.isoeng-
dc.publisherAmerican Chemical Society (ACS)en
dc.rightsCopyright © 2021 American Chemical Societyen
dc.rightsThis is an open access article published under a Creative Commons Non-Commercial NoDerivative Works (CC-BY-NC-ND) Attribution License, which permits copying and redistribution of the article, and creation of adaptations, all for non-commercial purposes.en
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/-
dc.subjectα-aminoisobutyric aciden
dc.subjectamphiphilic helixen
dc.subjectsynthetic mitochondria-targeting peptideen
dc.subjectTom20-recognition consensus sequenceen
dc.titleSynthetic Mitochondria-Targeting Peptides Incorporating α-Aminoisobutyric Acid with a Stable Amphiphilic Helix Conformation in Plant Cellsen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleACS Biomaterials Science & Engineeringen
dc.identifier.volume7-
dc.identifier.issue4-
dc.identifier.spage1475-
dc.identifier.epage1484-
dc.relation.doi10.1021/acsbiomaterials.0c01533-
dc.textversionpublisher-
dc.identifier.pmid33606492-
dcterms.accessRightsopen access-
datacite.awardNumber20K05718-
datacite.awardNumber.urihttps://kaken.nii.ac.jp/grant/KAKENHI-PROJECT-20K05718/-
dc.identifier.eissn2373-9878-
jpcoar.funderName日本学術振興会ja
jpcoar.awardTitle植物ミトコンドリア移行性を示す膜透過性ペプチドの創製ja
出現コレクション:学術雑誌掲載論文等

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