Enabling nanopore technology for sensing individual amino acids by a derivatization strategy-Reference-Cited by-同舟云学术

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Enabling nanopore technology for sensing individual amino acids by a derivatization strategy

Published:2020 Issue:31 Volume:8 Page:6792-6797
ISSN:2050-750X
Container-title:Journal of Materials Chemistry B
language:en
Short-container-title:J. Mater. Chem. B

Author:

Wei Xiaojun¹²³⁴⁵^ORCID,Ma Dumei⁶²³⁴⁷,Jing Lihong⁸⁹¹⁰¹¹¹²^ORCID,Wang Leon Y.⁵²³⁴,Wang Xiaoqin⁵²³⁴,Zhang Zehui¹²³⁴,Lenhart Brian J.⁵²³⁴,Yin Yingwu⁷¹³¹⁴¹⁵¹⁶^ORCID,Wang Qian⁶²³⁴^ORCID,Liu Chang¹²³⁴⁵^ORCID

Affiliation:

1. Biomedical Engineering Program

2. University of South Carolina

3. Columbia

4. USA

5. Department of Chemical Engineering

6. Department of Chemistry and Biochemistry

7. Department of Chemical and Biochemical Engineering

8. Key Laboratory of Colloid

9. Interface and Chemical Thermodynamics

10. Institute of Chemistry

11. Chinese Academy of Sciences

12. Beijing 100190

13. College of Chemistry and Chemical Engineering

14. Xiamen University

15. Xiamen 361005

16. China

Abstract

A derivatization strategy was demonstrated for reliable identification of individual amino acids using an α-hemolysin nanopore.

Funder

Youth Innovation Promotion Association of the Chinese Academy of Sciences

National Institute of Allergy and Infectious Diseases

National Institute of General Medical Sciences

National Natural Science Foundation of China

University of South Carolina

China Scholarship Council

Publisher

Royal Society of Chemistry (RSC)

Subject

General Materials Science,Biomedical Engineering,General Chemistry,General Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/2020/TB/D0TB00895H

Reference51 articles.

1. Self-assembling peptide and protein amyloids: from structure to tailored function in nanotechnology

2. Protein-mimetic peptide nanofibers: Motif design, self-assembly synthesis, and sequence-specific biomedical applications

3. Nanopore‐Based Protein Sequencing Using Biopores: Current Achievements and Open Challenges

4. NOTCH2 Mutations Cause Alagille Syndrome, a Heterogeneous Disorder of the Notch Signaling Pathway

5. WNT Signaling Pathway and Stem Cell Signaling Network: Fig. 1.

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