Nanopore‐Based Protein Deceleration and Sensing Using Graphene/Si3N4 Dual Membrane Cavity

Advanced Science

卷:13

RESEARCH ARTICLE

Yubin Cao¹  Junzhou He¹  Wei Si¹ 

[1] Jiangsu Key Laboratory for Design and Manufacturing of Precision Medicine Equipment, School of Mechanical Engineering, Southeast University, Nanjing, China

关键词: cavity structure;    deceleration;    nanopore;    protein sequencing;    translocation rate;   

DOI  :  10.1002/advs.76099

 received in 2026-02-27, accepted in 2026-05-29,  发布年份 2026

来源: Wiley

【 摘 要 】

ABSTRACTSequencing of protein with nanopores has emerged as a powerful tool offering rapid readout, high accuracy, low cost, and portability. There is an urgent need to improve the sensing accuracy of nanopores to effectively realize protein sequencing. However, controlling protein translocation rates remains a significant challenge. This study designed a graphene/Si3N4 dual membrane cavity system to explore potential solutions for enhancing protein sequencing accuracy and efficiency. Charge regulation and cavity structure were employed to slow down the translocation rate of peptides in the Si3N4 nanopore. The proposed Si3N4 toroidal cavity structure successfully reduces peptide translocation rates by introducing physical steric hindrance and enhancing van der Waals adsorption. This structure not only substantially prolongs peptide residence time in the sensing region but also maintains excellent signal resolution, offering a potential approach to address the high bandwidth demands in single‐molecule protein sequencing. The findings contribute to achieving high‐resolution, high‐throughput protein sequencing and advance the field of proteomics.

【 授权许可】

CC BY   
© 2026 The Author(s). Advanced Science published by Wiley‐VCH GmbH

【 图 表 】

Fig. 1