| Literature DB >> 32403927 |
Xiaojun Wei1,2, Dumei Ma3,4, Zehui Zhang1, Leon Y Wang2, Jonathan L Gray1, Libo Zhang3, Tianyu Zhu3, Xiaoqin Wang2, Brian J Lenhart2, Yingwu Yin4, Qian Wang3, Chang Liu1,2.
Abstract
Nanopore technology has been employed as a powerful tool for DNA sequencing and analysis. To extend this method to peptide sequencing, a necessary step is to profile individual amino acids (AAs) through their nanopore stochastic signals, which remains a great challenge because of the low signal-to-noise ratio and unpredictable conformational changes of AAs during their translocation through nanopores. We showed that the combination of an N-terminal derivatization strategy of AAs with nanopore technology could lead to effective in situ differentiation of AAs. Four different derivatization reactions have been tested with five selected AAs: Ala, Phe, Tyr, His, and Asp. Using an α-hemolysin nanopore, we demonstrated the feasibility of derivatization-assisted identification of AAs regardless of their charge composition and polarity. The method was further applied to discriminate each individual AA in testing data sets using their established nanopore profiles from training data sets. We envision that this proof-of-concept study will not only pave a way for identification of individual AAs but also lead to future applications in protein/peptide sequencing using the nanopore technology.Entities:
Keywords: amino acid; derivatization; identification; nanopore; proteomics
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Year: 2020 PMID: 32403927 PMCID: PMC7978492 DOI: 10.1021/acssensors.0c00345
Source DB: PubMed Journal: ACS Sens ISSN: 2379-3694 Impact factor: 7.711