Atomic force microscopy study of EDTA induced desorption of metal ions immobilized DNA from mica surface

被引:3
|
作者
Yang Tao [1 ]
Gao Hongyun [1 ]
机构
[1] Hebei Univ, Key Lab Med Chem & Mol Diag, Minist Educ, Coll Chem & Environm Sci, Baoding 071002, Peoples R China
关键词
DNA; Desorption; EDTA; AFM; Mica; ADSORPTION; ORIGAMI; BINDING; AIR; PURIFICATION; MOLECULES; ASSAY; RNA;
D O I
10.1016/j.ultramic.2019.01.001
中图分类号
TH742 [显微镜];
学科分类号
摘要
Adsorption of DNA molecules onto substrate, such as mica, is well documented. However, desorption of the immobilized DNA molecules from substrate, which is also an important aspect of DNA behavior on substrate, has not been paid much attention. Here, DNA molecules were first immobilized on mica surface by using divalent metal ions as the bridge agents. Desorption of the immobilized DNA from mica surface was realized via ethylenediamine tetraacetic acid disodium salt (EDTA) treatment. EDTA is a chelating agent; it can remove the bridging metal ions between DNA and mica, which leads to the release of DNA molecules from mica substrate. The divalent metal ions assisted DNA adsorption onto mica surface and the EDTA induced DNA desorption from mica surface were followed by atomic force microscopy (AFM). Randomly dispersed DNA strands and DNA networks are two distinct adsorption morphologies of DNA on mica surface and their desorption processes from mica surface induced by EDTA are also different. Other factors that influence the EDTA-induced DNA desorption, such as type of bridging metal ion and DNA molecule length, have also been systematically studied. Moreover, EDTA treatment has no effect on the integrity of DNA molecule. The EDTA induced desorption of metal ions immobilized DNA from mica surface is simple and effective, which has potential applications in DNA separation and purification, DNA biophysics, and DNA-based nanotechnology.
引用
收藏
页码:7 / 15
页数:9
相关论文
共 50 条
  • [1] DNA adsorption and desorption on mica surface studied by atomic force microscopy
    Sun, Lanlan
    Zhao, Dongxu
    Zhang, Yue
    Xu, Fugang
    Li, Zhuang
    APPLIED SURFACE SCIENCE, 2011, 257 (15) : 6560 - 6567
  • [2] Study of DNA immobilization on mica surface by atomic force microscopy
    Hornakova, Veronika
    Pribyl, Jan
    Skladal, Petr
    MONATSHEFTE FUR CHEMIE, 2016, 147 (05): : 865 - 871
  • [3] Disassembly of DNA-ligand on mica surface: atomic force microscopy studies
    Song, Y.
    Wang, L.
    Zhao, S.
    Lian, W.
    Li, Z.
    JOURNAL OF MICROSCOPY, 2009, 234 (02) : 130 - 136
  • [4] Study of DNA immobilization on mica surface by atomic force microscopy
    Veronika Horňáková
    Jan Přibyl
    Petr Skládal
    Monatshefte für Chemie - Chemical Monthly, 2016, 147 : 865 - 871
  • [5] Observation of the mica surface by atomic force microscopy
    Liu, ZG
    Li, Z
    Zhou, HL
    Wei, G
    Song, YH
    Wang, L
    MICRON, 2005, 36 (06) : 525 - 531
  • [6] Imaging DNA molecules on mica surface by atomic force microscopy in air and in liquid
    Liu, ZG
    Li, Z
    Zhou, HL
    Wei, G
    Song, YH
    Wang, L
    MICROSCOPY RESEARCH AND TECHNIQUE, 2005, 66 (04) : 179 - 185
  • [7] ATOMIC FORCE MICROSCOPY OF DNA ON MICA AND CHEMICALLY MODIFIED MICA
    THUNDAT, T
    ALLISON, DP
    WARMACK, RJ
    BROWN, GM
    JACOBSON, KB
    SCHRICK, JJ
    FERRELL, TL
    SCANNING MICROSCOPY, 1992, 6 (04) : 911 - 918
  • [8] Magnesium-Free Immobilization of DNA Origami Nanostructures at Mica Surfaces for Atomic Force Microscopy
    Xin, Yang
    Zargariantabrizi, Amir Ardalan
    Grundmeier, Guido
    Keller, Adrian
    MOLECULES, 2021, 26 (16):
  • [9] Mapping of Surface-Immobilized DNA with Force-Based Atomic Force Microscopy
    Lee, Yoonhee
    Kwon, Sung Hong
    Kim, Youngkyu
    Lee, Jong-Bong
    Park, Joon Won
    ANALYTICAL CHEMISTRY, 2013, 85 (08) : 4045 - 4050
  • [10] Probing Interactions between Aggrecan and Mica Surface by the Atomic Force Microscopy
    Chandran, Preethi L.
    Dimitriadis, Emilios K.
    Basser, Peter J.
    Horkay, Ferenc
    JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2010, 48 (24) : 2575 - 2581