Site‐Specific and Regioselective Modification of Human Epidermal Growth Factor Receptor 2 via Site‐Sculpted DNA Nanorefiners

C Chuangyuan Zhao (CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences) W Wenhao Shi (Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry) X Xiaowei Li (College of Chemistry, Institute of Nuclear Science and Technology, Key Laboratory of Radiation Physics and Technology of Ministry of Education) Y Yang Ying Y Yu Jin (Department of Pharmacy, The First Affiliated Hospital of University of Science and Technology of China (USTC), and School of Biomedical Engineering, Division of Life Sciences and Medicine, and Hefei National Research Center for Physical Sciences at the Microscale) G Guizhi Dong (CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences) D Dongsheng Liu (Department of Chemistry) Y Yuanchen Dong (CAS Key Laboratory of Colloid Interface and Chemical Thermodynamics, Beijing National Laboratory for Molecular Sciences, Institute of Chemistry)

Abstract

Abstract The site‐specific modification of native proteins is essential for regulating their functions and behaviors in biological systems. Such modifications enable advanced studies, but existing artificial methods often lack site selectivity and may perturb the functional integrity of the native proteins. In this study, we have developed a programmable platform based on site‐sculpted DNA nanorefiners (SS‐DNRs), which enables site‐specific modifications of proteins at multiple spatially defined sites through precise molecular recognition. Using the human epidermal growth factor receptor 2 (HER2) as a model system, we demonstrate that this approach could achieve precise site‐specific and regioselective modifications at multiple distinct sites without perturbing its intrinsic activity. By leveraging the programmability and addressability of DNA nanostructures, our platform effectively addresses fundamental challenges related to molecular selectivity and site selectivity that are inherent in chemical, enzymatic, genetic, and affinity‐based modification strategies.

Article Details

Volume / Issue Vol. 65, Issue 5
Published January 28, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

C

Chuangyuan Zhao

CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences

W

Wenhao Shi

Key Laboratory of Bioorganic Phosphorus Chemistry and Chemical Biology (Ministry of Education), Department of Chemistry

X

Xiaowei Li

College of Chemistry, Institute of Nuclear Science and Technology, Key Laboratory of Radiation Physics and Technology of Ministry of Education

Y

Yang Ying

Y

Yu Jin

Department of Pharmacy, The First Affiliated Hospital of University of Science and Technology of China (USTC), and School of Biomedical Engineering, Division of Life Sciences and Medicine, and Hefei National Research Center for Physical Sciences at the Microscale

G

Guizhi Dong

CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences

D

Dongsheng Liu

Department of Chemistry

Y

Yuanchen Dong

CAS Key Laboratory of Colloid Interface and Chemical Thermodynamics, Beijing National Laboratory for Molecular Sciences, Institute of Chemistry