纳米孔
纳米孔测序
蛋白质组学
计算生物学
化学
肽
分子
分子生物物理学
氨基酸
DNA测序
纳米技术
生物物理学
材料科学
生物
DNA
基因
生物化学
有机化学
作者
Zheng‐Li Hu,Ming‐Zhu Huo,Yi‐Lun Ying,Yi‐Tao Long
标识
DOI:10.1002/anie.202013462
摘要
Abstract Proteins are responsible for the occurrence and treatment of many diseases, and therefore protein sequencing will revolutionize proteomics and clinical diagnostics. Biological nanopore approach has proved successful for single‐molecule DNA sequencing, which resolves the identities of 4 natural deoxyribonucleotides based on the current blockages and duration times of their translocations across the nanopore confinement. However, open challenges still remain for biological nanopores to sequentially identify each amino acid (AA) of single proteins due to the inherent complexity of 20 proteinogenic AAs in charges, volumes, hydrophobicity and structures. Herein, we focus on recent exciting advances in biological nanopores for single‐molecule protein sequencing (SMPS) from native protein unfolding, control of peptide translocation, AA identification to applications in disease detection.
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