Updated on 2026/01/09

写真a

 
KOHATA AI
 
Organization
School of Life Science and Technology Assistant Professor
Title
Assistant Professor
External link

Degree

  • Ph.D. Engineering ( The University of Tokyo )

Education

  • The University of Tokyo   The Graduate School of Engineering   Department of Chemistry and Biotechnology

    2017.4 - 2022.3

      More details

Research History

  • Institute of Science Tokyo   School of Life Science and Technology   Assistant Professor

    2024.10

      More details

  • Tokyo Institute of Technology   School of Life Science and Technology   Assistant Professor

    2023.7 - 2024.9

      More details

  • The University of Tokyo   The Graduate School of Engineering, Department of Chemistry and Biotechnology   Project Assistant Professor

    2022.4 - 2023.6

      More details

  • The University of Tokyo   The Graduate School of Engineering, Department of Chemistry and Biotechnology   JSPS Research Fellow

    2019.4 - 2022.3

      More details

Papers

  • Effect of PEG Chain Length on the Water Solubility of Monodisperse PEG-Appended Molecules

    Rei Hamaguchi, Ai Kohata, Mafumi Hishida, Hiroka Sugai, Mitsunori Ikeguchi, Kazushi Kinbara

    2026.1

  • Facile Synthesis of 5‐Halo‐1,2,3‐triazole‐fused Benzotricyclic Frameworks from 1‐(ω‐Azidoalkyl)‐2‐(2,2‐dihalovinyl)arenes and their Application in Fluorescent Triazole Derivatives Reviewed

    Takeshi Hata, Seiya Kikukawa, Miki Ebihara, Kazuki Kobayashi, Nozomi Kasakura, Takashi Kanamori, Tadaomi Furuta, Ai Kohata, Nobuaki Funahashi, Shota Matsumoto, Satoru Karasawa, Kazushi Kinbara, Naohiko Koshikawa, Hideya Yuasa

    European Journal of Organic Chemistry   2025.6

     More details

    Publishing type:Research paper (scientific journal)   Publisher:Wiley  

    By heating 1‐(ω‐azidoalkyl)‐2‐(2,2‐dihalovinyl)arenes in DMF, intramolecular Huisgen cycloaddition between the azido group and the 1,1‐dihalovinyl moiety proceeded smoothly to afford 5‐halo‐1,2,3‐triazole‐fused tricyclic benzocondensed compounds. Leveraging the remaining halogen groups, carbon‐chain extension via Mizoroki–Heck or Suzuki–Miyaura coupling reactions, followed by an intramolecular Friedel–Crafts reaction, furnished polycyclic systems incorporating fused triazole rings. Furthermore, transformation of the halogen groups into 2‐nitrobenzene derivatives via Suzuki–Miyaura cross‐coupling, followed by a Cadogan reaction using triphenylphosphine, provided a series of fluorescent pentacyclic compounds.

    DOI: 10.1002/ejoc.202500355

    researchmap

  • Comparison of the effects of perfluoroalkyl and alkyl groups on cellular uptake in short peptides Reviewed International journal

    Koji Kadota, Ai Kohata, Shinsuke Sando, Jumpei Morimoto, Kohsuke Aikawa, Takashi Okazoe

    RSC advances   15 ( 11 )   8189 - 8194   2025.3

     More details

    Language:English   Publishing type:Research paper (scientific journal)  

    The differences in the effects of perfluoroalkyl (RF) and alkyl (RH) groups on the cellular uptake of short peptides were evaluated. A facile synthetic method was established to produce Fmoc-protected amino acids bearing RF and RH groups on their side chains. The synthesized Fmoc-protected amino acids were successfully incorporated into peptides using solid-phase peptide synthesis. Peptides with an RF group exhibited higher cellular uptake efficiency compared to peptides with an RH group of the same side-chain length. Intriguingly, the cytotoxicity of the AF647-RF-tripeptide (RF = C8F17) was lower than that of the AF647-RH-tripeptide (RH = C12H25), despite similar cellular uptake efficiencies. An evaluation of the binding affinity of the peptides to liposome membranes suggested that the higher lipophobicity of the RF group, compared to the RH group, contributed to the lower cytotoxicity observed in the peptide with the RF group. These findings indicate that the introduction of an RF group into peptides has considerable potential for developing drug-delivery carriers with enhanced uptake efficiency and low cytotoxicity.

    DOI: 10.1039/d5ra00304k

    PubMed

    researchmap

  • Synthetic ion channels in biomembranes Reviewed

    Ai Kohata, Kazushi Kinbara

    Current Opinion in Chemical Biology   84   102544 - 102544   2025.2

     More details

    Authorship:Lead author   Publishing type:Research paper (scientific journal)   Publisher:Elsevier BV  

    DOI: 10.1016/j.cbpa.2024.102544

    researchmap

  • Highly Alternating Copolymer of [1.1.1]Propellane and Perfluoro Vinyl Ether: Forming a Hydrophobic and Oleophobic Surface with <50% Fluorine Monomer Content Reviewed

    Mizuki Okuda, Midori Akiyama, Kosuke Funahashi, Junki Masuda, Ai Kohata, Shintaro Nakagawa, Kimiaki Kashiwagi, Norihide Sugiyama, Takashi Okazoe, Daisuke Kawaguchi

    ACS Macro Letters   2024.11

     More details

    Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/acsmacrolett.4c00558

    researchmap

  • Fluoro-Crown Ether Phosphate as Efficient Cell-Permeable Drug Carrier by Disrupting Hydration Layer Reviewed

    Abir Goswami, Ai Kohata, Takashi Okazoe, Hubiao Huang, Takuzo Aida

    Journal of the American Chemical Society   2024.8

     More details

    Authorship:Lead author   Publishing type:Research paper (scientific journal)  

    DOI: 10.1021/jacs.4c06464

    researchmap

  • Generating synthetic gap junctions using supramolecular amphiphilic giant nanotubes Invited Reviewed

    Ai Kohata, Kazushi Kinbara

    Nature Chemistry   16 ( 9 )   1387 - 1389   2024.8

     More details

    Authorship:Lead author   Publishing type:Research paper (scientific journal)   Publisher:Springer Science and Business Media LLC  

    DOI: 10.1038/s41557-024-01604-y

    researchmap

    Other Link: https://www.nature.com/articles/s41557-024-01604-y

  • Monitoring insulin fibrillation kinetics using chromatographic analysis Reviewed

    Pituwala Kankanamge Thirasara Sammani, Wijak Yospanya, Tatsuya Niwa, Ai Kohata, Hideki Taguchi, Kazushi Kinbara

    International Journal of Biological Macromolecules   275   133660 - 133660   2024.8

     More details

    Publishing type:Research paper (scientific journal)   Publisher:Elsevier BV  

    DOI: 10.1016/j.ijbiomac.2024.133660

    researchmap

  • Fluorocarbon–DNA conjugates for enhanced cellular delivery: Formation of a densely packed DNA nano‐assembly Reviewed

    Minako Narita, Ai Kohata, Taiichi Kageyama, Honoka Watanabe, Kohsuke Aikawa, Daisuke Kawaguchi, Kunihiko Morihiro, Akimitsu Okamoto, Takashi Okazoe

    ChemBioChem   2024.6

     More details

    Authorship:Corresponding author   Publishing type:Research paper (scientific journal)   Publisher:Wiley  

    Forming nano‐assemblies is essential for delivering DNA conjugates into cells, with the DNA density in the nano‐assembly playing an important role in determining the uptake efficiency. In this study, we developed a strategy for the facile synthesis of DNA strands bearing perfluoroalkyl (RF) groups (RF‐DNA conjugates) and investigated how they affect cellular uptake. An RF‐DNA conjugate bearing a long RF group at the DNA terminus forms a nano‐assembly with a high DNA density, which results in greatly enhanced cellular uptake. The uptake mechanism is mediated by clathrin‐dependent endocytosis. The use of RF groups to densely assemble negatively charged DNA is a useful strategy for designing drug delivery carriers.

    DOI: 10.1002/cbic.202400436

    researchmap

  • Synthesis of Short Peptides with Perfluoroalkyl Side Chains and Evaluation of Their Cellular Uptake Efficiency Reviewed

    Koji Kadota, Toshiki Mikami, Ai Kohata, Jumpei Morimoto, Shinsuke Sando, Kohsuke Aikawa, Takashi Okazoe

    ChemBioChem   2023.7

     More details

    Publishing type:Research paper (scientific journal)  

    DOI: 10.1002/cbic.202300374

    Scopus

    PubMed

    researchmap

  • Reconstitution of microtubule into GTP-responsive nanocapsules Reviewed

    Noriyuki Uchida, Ai Kohata, Kou Okuro, Annalisa Cardellini, Chiara Lionello, Eric A. Zizzi, Marco A. Deriu, Giovanni M. Pavan, Michio Tomishige, Takaaki Hikima, Takuzo Aida

    Nature Communications   13 ( 1 )   2022.9

     More details

    Publishing type:Research paper (scientific journal)   Publisher:Springer Science and Business Media LLC  

    Abstract

    Nanocapsules that collapse in response to guanosine triphosphate (GTP) have the potential as drug carriers for efficiently curing diseases caused by cancer and RNA viruses because GTP is present at high levels in such diseased cells and tissues. However, known GTP-responsive carriers also respond to adenosine triphosphate (ATP), which is abundant in normal cells as well. Here, we report the elaborate reconstitution of microtubule into a nanocapsule that selectively responds to GTP. When the tubulin monomer from microtubule is incubated at 37 °C with a mixture of GTP (17 mol%) and nonhydrolysable GTP* (83 mol%), a tubulin nanosheet forms. Upon addition of photoreactive molecular glue to the resulting dispersion, the nanosheet is transformed into a nanocapsule. Cell death results when a doxorubicin-containing nanocapsule, after photochemically crosslinked for properly stabilizing its shell, is taken up into cancer cells that overexpress GTP.

    DOI: 10.1038/s41467-022-33156-5

    researchmap

    Other Link: https://www.nature.com/articles/s41467-022-33156-5

  • Photoreactive Molecular Glue for Enhancing the Efficacy of DNA Aptamers by Temporary-to-Permanent Conjugation with Target Proteins Reviewed

    Ai Kohata, Ryosuke Ueki, Kou Okuro, P. K. Hashim, Shinsuke S, Takuzo Aida

    Journal of the American Chemical Society   143 ( 34 )   13937 - 13943   2021.8

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:American Chemical Society ({ACS})  

    DOI: 10.1021/jacs.1c06816

    researchmap

  • Transferrin-Appended Nanocaplet for Transcellular siRNA Delivery into Deep Tissues Reviewed

    Ai Kohata, P. K. Hashim, Kou Okuro, Takuzo Aida

    Journal of the American Chemical Society   141 ( 7 )   2862 - 2866   2019.2

     More details

    Authorship:Lead author   Language:English   Publishing type:Research paper (scientific journal)   Publisher:American Chemical Society ({ACS})  

    DOI: 10.1021/jacs.8b12501

    researchmap

▼display all

Books

  • 月刊「細胞」

    木幡 愛( Role: Joint authorTopics from special edition「高度にフッ素化された化合物による薬物送達」p.76–79)

    ニューサイエンス社  2025.9 

     More details

  • 有機フッ素化合物の合成と応用最前線 = Frontiers in the synthesis and application of organofluorine compounds

    木幡 愛( Role: Joint author第2章 1 高度にフッ素化された化合物による核酸の細胞内送達)

    シーエムシー出版  2025.1  ( ISBN:9784781318585

     More details

    Total pages:v, 293p   Language:Japanese  

    CiNii Books

    researchmap

  • 新規モダリティ医薬品のためのDDS技術とその製剤化

    岡添隆, 相川光介, 木幡愛( Role: Joint authorペルフルオロ構造を利用したペプチドや核酸の細胞内送達技術, 第6章 第8節 pp.325-332.)

    (株)技術情報協会  2023.1 

     More details

Research Projects

  • 脂質膜表面で駆動し、ベシクルを変形させる巨大な分子機械

    2025.10 - 2028.3

    科学技術振興機構  戦略的創造研究推進事業 ACT-X 

      More details

  • 水面に浮かぶ自励振動油滴の化学的な動態制御

    2025.7 - 2026.6

    東京科学大学  2025年度 あすなろ研究奨励金 

      More details

  • ベシクルの機能化のための人工シグナル伝達分子

    Grant number:25K18070  2025.4 - 2027.3

    日本学術振興会  科学研究費助成事業  若手研究

    木幡 愛

      More details

    Grant amount:\4680000 ( Direct Cost: \3600000 、 Indirect Cost:\1080000 )

    researchmap

  • 会合型の人工膜貫通分子による細胞内シグナル伝達

    2025.4 - 2027.3

    中谷医工計測技術振興財団  2025年度 研究助成 [奨励研究] 

      More details

  • 新規フッ素化合物による粘膜透過

    2023.4 - 2025.3

    花王芸術・科学財団  第2回 花王 Crescent Award 

      More details

  • 経粘膜送達のための新規フッ素化合物の開拓

    Grant number:23K13852  2023.4 - 2025.3

    日本学術振興会  科学研究費助成事業  若手研究

    木幡 愛

      More details

    Grant amount:\4550000 ( Direct Cost: \3500000 、 Indirect Cost:\1050000 )

    researchmap

  • 特異な体内動態を実現するタンパク質修飾siRNA内包ナノカプセル

    Grant number:19J22946  2019.4 - 2022.3

    日本学術振興会  科学研究費助成事業 特別研究員奨励費  特別研究員奨励費

    木幡 愛

      More details

    Grant amount:\3100000 ( Direct Cost: \3100000 )

    これまでにトランスフェリン修飾siRNA 内包ナノカプセルを開発し、癌組織深部へとsiRNAを送達する輸送体の開発に成功している。さらに、このsiRNA内包ナノカプセルの体内動態は表面に導入するタンパク質によって制御できることを明らかにした。
    このナノカプセルの開発において、本研究者は核酸やタンパク質に強い接着性を有する『分子糊』を利用した。分子糊は多数のグアニジニウム基を有し、生体高分子表面のオキシアニオン性官能基と多価的に塩橋を形成する。そこで今年度はこの分子糊を応用し、DNA・RNAなどの核酸表面を修飾する分子ツール開発に乗り出した。具体的には核酸医薬DNAアプタマーの生医学的な応用を指向した光反応性分子糊の開発を行なった。
    DNAアプタマーはその標的選択性の高さから抗体に代わる合成医薬として注目されている。しかしながら、DNAアプタマーは標的タンパク質に対して非共有結合的に接着するため、結合力が不十分であることが課題である。 そこで本研究では、アプタマー/標的タンパク質複合体を、共有結合的に安定化することのできる光反応性分子糊を合成した。この分子糊を用いて光照射を施すことにより、DNAアプタマーを標的タンパク質上へ固定化し、アプタマーの阻害効果を増強することができる。一例として癌細胞の遊走や増殖を阻害するSL1アプタマーおよびその標的受容体タンパク質c-Metを用いて、SL1アプタマーの阻害効果増強を細胞遊走実験によって評価した。

    researchmap

▼display all