

FOLLOWUS
a.State Key Laboratory of Advanced Fiber Materials, Center for Advanced Low-Dimension Materials, Donghua University, Shanghai 201620, China
b.Salus BioMed Company, Shenzhen 518106, China
c.Institute of Advanced Technology, University of Science and Technology of China, Hefei 230026, China
jinyk@mail.ustc.edu.cn (Y.K.J.)
lihui@dhu.edu.cn (H.L.)
liuh@dhu.edu.cn (H.L.)
Received:10 June 2025,
Revised:2025-07-09,
Accepted:09 July 2025,
Online First:02 September 2025,
Published:05 November 2025
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Tian, W.; Wang, X. Y.; Feng, D. W.; Li, X. Q.; Jin, Y. K.; Li, H.; Liu, H. Amine-reactive polymer platform for engineering surface modification of next-generation sequencing chips. Chinese J. Polym. Sci. 2025, 43, 2030–2041
Wei Tian, Xin-Yuan Wang, Die-Wen Feng, et al. Amine-reactive Polymer Platform for Engineering Surface Modification of Next-generation Sequencing Chips[J]. Chinese Journal of Polymer Science, 2025, 43(11): 2030-2041.
Tian, W.; Wang, X. Y.; Feng, D. W.; Li, X. Q.; Jin, Y. K.; Li, H.; Liu, H. Amine-reactive polymer platform for engineering surface modification of next-generation sequencing chips. Chinese J. Polym. Sci. 2025, 43, 2030–2041 DOI: 10.1007/s10118-025-3413-8.
Wei Tian, Xin-Yuan Wang, Die-Wen Feng, et al. Amine-reactive Polymer Platform for Engineering Surface Modification of Next-generation Sequencing Chips[J]. Chinese Journal of Polymer Science, 2025, 43(11): 2030-2041. DOI: 10.1007/s10118-025-3413-8.
Part (a) illustrates the post-polymerization modification of the PPFPA platform with Monomer-1 and Monomer-2
introducing azide groups and hydrophilic functionalities. Part (b) shows the covalent anchoring of the surface modification polymer onto the sequencing chip surface via click chemistry.
In this study
an amine-reactive poly(pentafluorophenyl acrylate) (
PPFPA
) platform was developed for advanced surface engineering of next-generation sequencing (NGS) chips. Through post-polymerization modification
PPFPA
was functionalized with dual moieties: azide groups for covalent immobilization of DBCO-modified DNA primers
via
click chemistry and tunable hydrophilic side chains to optimize biocompatibility and surface properties. Systematic screening revealed that hydrophobic azide carriers combined with neutral hydroxyl groups maximized the DNA immobilization efficacy
approaching the performance of commercial polyacrylamide-based polymers. The negatively charged carboxyl groups severely impede DNA primer attachment. Higher molecular weight derivatives further enhance the efficacy of DNA immobilization. In NGS validation
optimized surface modification polymers achieved robust surface density of clustered DNA and high sequencing accuracy
surpassing quality benchmarks and comparable to those of conventional analogs. This platform demonstrates significant potential for tailoring high-sensitivity surfaces for genomic applications
advancing clinical diagnostics
and personalized medicine.
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