Lu Chunzhe, Bonini Andrea, Viel Jakob H, Maglia Giovanni
University of Groningen, Chemical Biology Department, Groningen Biomolecular Sciences and Biotechnology, Groningen, Netherlands.
Nat Biotechnol. 2025 Mar;43(3):312-322. doi: 10.1038/s41587-025-02587-y. Epub 2025 Mar 17.
Over the past three decades, biological nanopore sequencing has grown from a research curiosity to a mature technology to sequence nucleic acids at the single-molecule level. Now, recent achievements suggest that nanopores might be able to sequence proteins soon. In this Perspective, we analyze the different approaches that have been proposed to measure proteins and peptides using nanopores. We predict that, more likely than not, nanopores will be capable of identifying full-length proteins at the single-molecule level and with single-amino acid resolution, paving the way to single-molecule protein sequencing. This would allow several applications in proteomics that are at present challenging, including measuring the heterogeneity of post-translational modifications, quantifying low-abundance proteins and characterizing protein splicing.
在过去三十年里,生物纳米孔测序已从一项仅供研究好奇的技术发展成为一项能在单分子水平对核酸进行测序的成熟技术。如今,近期的成果表明纳米孔或许很快就能对蛋白质进行测序。在这篇观点文章中,我们分析了已被提出的利用纳米孔测量蛋白质和肽段的不同方法。我们预测,纳米孔极有可能在单分子水平上以单氨基酸分辨率识别全长蛋白质,从而为单分子蛋白质测序铺平道路。这将使蛋白质组学中目前颇具挑战性的多项应用成为可能,包括测量翻译后修饰的异质性、定量低丰度蛋白质以及表征蛋白质剪接。