N‑Terminal Derivatization-Assisted Identification of Individual Amino Acids Using a Biological Nanopore Sensor
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-n...
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Published in: | ACS sensors Vol. 5; no. 6; pp. 1707 - 1716 |
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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. |
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AbstractList | 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. 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 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. 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. |
Author | Zhang, Libo Ma, Dumei Gray, Jonathan L Zhu, Tianyu Zhang, Zehui Wang, Leon Y Yin, Yingwu Wang, Qian Lenhart, Brian J Wei, Xiaojun Wang, Xiaoqin Liu, Chang |
AuthorAffiliation | Department of Chemistry and Biochemistry Department of Chemical Engineering Department of Chemical and Biochemical Engineering, College of Chemistry and Chemical Engineering Biomedical Engineering Program University of South Carolina |
AuthorAffiliation_xml | – name: Department of Chemical Engineering – name: Biomedical Engineering Program – name: University of South Carolina – name: Department of Chemical and Biochemical Engineering, College of Chemistry and Chemical Engineering – name: Department of Chemistry and Biochemistry |
Author_xml | – sequence: 1 givenname: Xiaojun surname: Wei fullname: Wei, Xiaojun organization: University of South Carolina – sequence: 2 givenname: Dumei surname: Ma fullname: Ma, Dumei organization: Department of Chemical and Biochemical Engineering, College of Chemistry and Chemical Engineering – sequence: 3 givenname: Zehui surname: Zhang fullname: Zhang, Zehui organization: Biomedical Engineering Program – sequence: 4 givenname: Leon Y surname: Wang fullname: Wang, Leon Y organization: University of South Carolina – sequence: 5 givenname: Jonathan L surname: Gray fullname: Gray, Jonathan L organization: Biomedical Engineering Program – sequence: 6 givenname: Libo surname: Zhang fullname: Zhang, Libo organization: University of South Carolina – sequence: 7 givenname: Tianyu orcidid: 0000-0001-9115-6462 surname: Zhu fullname: Zhu, Tianyu organization: University of South Carolina – sequence: 8 givenname: Xiaoqin surname: Wang fullname: Wang, Xiaoqin organization: University of South Carolina – sequence: 9 givenname: Brian J surname: Lenhart fullname: Lenhart, Brian J organization: University of South Carolina – sequence: 10 givenname: Yingwu orcidid: 0000-0002-9123-7761 surname: Yin fullname: Yin, Yingwu organization: Department of Chemical and Biochemical Engineering, College of Chemistry and Chemical Engineering – sequence: 11 givenname: Qian orcidid: 0000-0002-2149-384X surname: Wang fullname: Wang, Qian email: wang263@mailbox.sc.edu organization: University of South Carolina – sequence: 12 givenname: Chang orcidid: 0000-0001-8097-9631 surname: Liu fullname: Liu, Chang email: changliu@cec.sc.edu organization: University of South Carolina |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Author Contributions X.W. and D.M. contributed equally to this work. X.W., D.M., Z.Z., Q.W., and C.L. designed the experiments. Q.W. and C.L. supervised the project: C.L. supervised the nanopore analysis; Q.W. and Y.Y. supervised the AA derivatization and analysis; C.L. and Q.W. supervised the data analysis. X.W. and D.M. primarily performed experiments and data analysis. Z.Z., L.Y.W., J.L.G., L.Z., T.Z., X-Q.W., and B.J.L. helped with experiments and data analysis. X.W., D.M., Y.Y., Q.W. and C.L. wrote the manuscript. |
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SubjectTerms | Amino Acid Sequence Amino Acids Hemolysin Proteins Nanopores Peptides |
Title | N‑Terminal Derivatization-Assisted Identification of Individual Amino Acids Using a Biological Nanopore Sensor |
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