A two-step calibration method for evaluation high bandwidth electrochemical instrument

被引:2
作者
Zhang, Lin-Lin [1 ]
Zhong, Cheng-Bing [1 ]
Li, Jun-Ge [1 ]
Niu, Hong-Yan [1 ]
Ying, Yi-Lun [1 ,2 ]
Long, Yi-Tao [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Life Sci, Nanjing 210023, Peoples R China
[2] Nanjing Univ, Chem & Biomed Innovat Ctr, Nanjing 210023, Peoples R China
关键词
Single-entity electrochemistry; High bandwidth; Electrochemical instrument; Nanopore; Low noise amplifier; Aerolysin; NANOPORE IDENTIFICATION; TRANSIENT CONFORMATIONS; AEROLYSIN NANOPORE; SINGLE;
D O I
10.1016/j.jelechem.2022.116266
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Single-entity electrochemistry allows the ultrasensitive detection of individual entities by incorporating high bandwidth electrochemical instruments. However, differences among instruments and shielding setups cause large deviations in the recorded signals, which leads to remarkable measurement errors in practical applications. Here, we developed a two-step method to calibrate instruments differences for achieving an accurate single-entity analysis. Two coefficients C1 and C2 were calculated with standard measurements through the model resistors of 1.00 G omega. C1 obtained from the slope value of the current-voltage (I-V) curve is used to calibrate the shifting of the current statistic distribution. Then, C2, assessed from the standard deviation (STD) noises, is employed to calibrate the full-width at half maximum of current statistic distributions. After applying the model single-molecule experiments of Poly(dA)4 detection with aerolysin nanopores, we showed the effective calibration of measurement differences among four kind of high bandwidth electrochemical instruments. Therefore, this method is generally applicable to nearly all kinds of single-entity electrochemical measurements to reduce measurement errors from instrument differences.
引用
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页数:6
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共 42 条
  • [1] [Anonymous], WE BUILD TOOLS SO YO
  • [2] Perspective and Prospectus on Single-Entity Electrochemistry
    Baker, Lane A.
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2018, 140 (46) : 15549 - 15559
  • [3] Multiple rereads of single proteins at single-amino acid resolution using nanopores
    Brinkerhoff, Henry
    Kang, Albert S. W.
    Liu, Jingqian
    Aksimentiev, Aleksei
    Dekker, Cees
    [J]. SCIENCE, 2021, 374 (6574) : 1509 - +
  • [4] Nanopore Identification of Single Nucleotide Mutations in Circulating Tumor DNA by Multiplexed Ligation
    Burck, Nitza
    Gilboa, Tal
    Gadi, Abhilash
    Nehrer, Michelle Patkin
    Schneider, Robert J.
    Meller, Amit
    [J]. CLINICAL CHEMISTRY, 2021, 67 (05) : 753 - 762
  • [5] Cao C, 2016, NAT NANOTECHNOL, V11, P713, DOI [10.1038/nnano.2016.66, 10.1038/NNANO.2016.66]
  • [6] Controlled movement of ssDNA conjugated peptide through Mycobacterium smegmatis porin A (MspA) nanopore by a helicase motor for peptide sequencing application
    Chen, Zhijie
    Wang, Zhenqin
    Xu, Yang
    Zhang, Xiaochun
    Tian, Boxue
    Bai, Jingwei
    [J]. CHEMICAL SCIENCE, 2021, 12 (47) : 15750 - 15756
  • [7] Nanopore blockade sensors for ultrasensitive detection of proteins in complex biological samples
    Chuah, Kyloon
    Wu, Yanfang
    Vivekchand, S. R. C.
    Gaus, Katharina
    Reece, Peter J.
    Micolich, Adam P.
    Gooding, J. Justin
    [J]. NATURE COMMUNICATIONS, 2019, 10 (1)
  • [8] A Low-Noise Transimpedance Amplifier for BLM-Based Ion Channel Recording
    Crescentini, Marco
    Bennati, Marco
    Saha, Shimul Chandra
    Ivica, Josip
    de Planque, Maurits
    Morgan, Hywel
    Tartagni, Marco
    [J]. SENSORS, 2016, 16 (05):
  • [9] Detection of single exosomes with a closed wireless nanopore electrode
    Cui, Lingfei
    Xu, Suwen
    Liang, Chi
    Yu, Rujia
    Li, Liang
    Ying, Yilun
    Long, Yitao
    [J]. CHINESE SCIENCE BULLETIN-CHINESE, 2020, 65 (01): : 60 - 66
  • [10] Single-Molecule Sensors: Challenges and Opportunities for Quantitative Analysis
    Gooding, J. Justin
    Gaus, Katharina
    [J]. ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2016, 55 (38) : 11354 - 11366