TY - JOUR
T1 - Homogeneous Oligomeric Ligands Prepared via Radical Polymerization that Recognize and Neutralize a Target Peptide
AU - Hoshino, Yu
AU - Taniguchi, Shohei
AU - Takimoto, Hinata
AU - Akashi, Sotaro
AU - Katakami, Sho
AU - Yonamine, Yusuke
AU - Miura, Yoshiko
N1 - Funding Information:
This research was supported by JSPS (23750193), JST A-STEP (AS2321466 and AS231Z01490D), AMED (JP17efk0108127h), Ogasawara Foundation, Kakihara Foundation, and Kao Foundation for Arts and Sciences.
Publisher Copyright:
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2020/1/7
Y1 - 2020/1/7
N2 - Abiotic ligands that bind to specific biomolecules have attracted attention as substitutes for biomolecular ligands, such as antibodies and aptamers. Radical polymerization enables the production of robust polymeric ligands from inexpensive functional monomers. However, little has been reported about the production of monodispersed polymeric ligands. Herein, we present homogeneous ligands prepared via radical polymerization that recognize epitope sequences on a target peptide and neutralize the toxicity of the peptide. Taking advantage of controlled radical polymerization and separation, a library of multifunctional oligomers with discrete numbers of functional groups was prepared. Affinity screening revealed that the sequence specificity of the oligomer ligands strongly depended on the number of functional groups. The process reported here will become a general step for the development of abiotic ligands that recognize specific peptide sequences.
AB - Abiotic ligands that bind to specific biomolecules have attracted attention as substitutes for biomolecular ligands, such as antibodies and aptamers. Radical polymerization enables the production of robust polymeric ligands from inexpensive functional monomers. However, little has been reported about the production of monodispersed polymeric ligands. Herein, we present homogeneous ligands prepared via radical polymerization that recognize epitope sequences on a target peptide and neutralize the toxicity of the peptide. Taking advantage of controlled radical polymerization and separation, a library of multifunctional oligomers with discrete numbers of functional groups was prepared. Affinity screening revealed that the sequence specificity of the oligomer ligands strongly depended on the number of functional groups. The process reported here will become a general step for the development of abiotic ligands that recognize specific peptide sequences.
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U2 - 10.1002/anie.201910558
DO - 10.1002/anie.201910558
M3 - Article
C2 - 31691476
AN - SCOPUS:85075723178
SN - 1433-7851
VL - 59
SP - 679
EP - 683
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 2
ER -