肽
纳米孔
序列(生物学)
肽序列
计算生物学
纳米孔测序
鉴定(生物学)
蛋白质测序
化学
序列分析
生物化学
蛋白质结构
生物
基序列
肽段
片段(逻辑)
计算机科学
DNA测序
识别序列
劈开
序列比对
肽库
纳米技术
作者
Ying-Huan FU,Nannan Wei,Kai-Li Xin,Xinyi Li,Li-Min Zhang,Cheng Yang,Feng Yan,Yi‐Tao Long,Yi‐Lun Ying
标识
DOI:10.1038/s41467-026-75942-5
摘要
Despite substantial progress in nanopore sensing, residue-by-residue peptide sequencing remains a major challenge. Herein, we present EANPSeq, an exopeptidase-assisted nanopore peptide identification strategy based on peptide libraries to decode the peptide sequence. By continuously recognizing the resulting fragments from digesting peptides stepwise through a nanopore, this approach could achieve the identification of peptide sequence based on the comparison of fragment data with libraries of shortened and mutated peptides, with the assistance of machine learning. Notably, compared with previously reported nanopore peptide sensing strategies, EANPSeq shows sufficient resolution to recognize the continuous sequence of peptides containing adjacent identical residues and to precisely localize post-translational modification (PTM) sites within consecutive residues. These proof-of-concept results highlight our nanopore-based strategy as a new avenue for single-molecule protein sequencing. There is significant interest in developing nanopore-based methods for peptide sensing and sequencing. Here the authors report, EANPSeq, a method which enables residue-by-residue peptide sequencing using an exopeptidase-assisted approach, decoding stepwise digestion fragments with machine-learning to achieve single-molecule sequence identification and PTM localization.
科研通智能强力驱动
Strongly Powered by AbleSci AI