Investigating Single Molecule Adhesion by Atomic Force Spectroscopy

被引:5
|
作者
Stetter, Frank W. S. [1 ,2 ]
Kienle, Sandra [1 ,2 ]
Krysiak, Stefanie [1 ,2 ]
Hugel, Thorsten [1 ,2 ]
机构
[1] Tech Univ Munich, Phys Dept E22a, D-80290 Munich, Germany
[2] Tech Univ Munich, IMETUM, D-80290 Munich, Germany
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2015年 / 96期
关键词
Physics; Issue; 96; AFM; functionalization; single molecule; polymer; lipid; adhesion; atomic force microscopy; force spectroscopy; POLYMER ADHESION; MICROSCOPY; ADSORPTION; MECHANICS; GOLD; TIPS;
D O I
10.3791/52456
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Atomic force spectroscopy is an ideal tool to study molecules at surfaces and interfaces. An experimental protocol to couple a large variety of single molecules covalently onto an AFM tip is presented. At the same time the AFM tip is passivated to prevent unspecific interactions between the tip and the substrate, which is a prerequisite to study single molecules attached to the AFM tip. Analyses to determine the adhesion force, the adhesion length, and the free energy of these molecules on solid surfaces and bio-interfaces are shortly presented and external references for further reading are provided. Example molecules are the poly(amino acid) polytyrosine, the graft polymer PI-g-PS and the phospholipid POPE (1-palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanolamine). These molecules are desorbed from different surfaces like CH3-SAMs, hydrogen terminated diamond and supported lipid bilayers under various solvent conditions. Finally, the advantages of force spectroscopic single molecule experiments are discussed including means to decide if truly a single molecule has been studied in the experiment.
引用
收藏
页数:11
相关论文
共 50 条
  • [1] Single molecule atomic force microscopy and force spectroscopy of chitosan
    Kocun, Marta
    Grandbois, Michel
    Cuccia, Louis A.
    COLLOIDS AND SURFACES B-BIOINTERFACES, 2011, 82 (02) : 470 - 476
  • [2] Covalent Immobilization of Proteins for the Single Molecule Force Spectroscopy
    Becke, Tanja D.
    Ness, Stefan
    Sudhop, Stefanie
    Gaub, Hermann E.
    Hilleringmann, Markus
    Schilling, Arndt F.
    Clausen-Schaumann, Hauke
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2018, (138):
  • [3] Force Spectroscopy of Single Protein Molecules Using an Atomic Force Microscope
    Scholl, Zackary N.
    Li, Qing
    Josephs, Eric
    Apostolidou, Dimitra
    Marszalek, Piotr E.
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2019, (144):
  • [4] Covalent Attachment of Single Molecules for AFM-based Force Spectroscopy
    Kolberg, Adrianna
    Wenzel, Christiane
    Hugel, Thorsten
    Gallei, Markus
    Balzer, Bizan N.
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2020, (157):
  • [5] Single molecule force spectroscopy in biology using the atomic force microscope
    Zlatanova, J
    Lindsay, SM
    Leuba, SH
    PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 2000, 74 (1-2) : 37 - 61
  • [6] Practical single molecule force spectroscopy: How to determine fundamental thermodynamic parameters of intermolecular bonds with an atomic force microscope
    Noy, Aleksandr
    Friddle, Raymond W.
    METHODS, 2013, 60 (02) : 142 - 150
  • [7] Single molecule binding dynamics measured with atomic force microscopy
    van Es, M. H.
    Tang, J.
    Preiner, J.
    Hinterdorfer, P.
    Oosterkamp, T. H.
    ULTRAMICROSCOPY, 2014, 140 : 32 - 36
  • [8] Application of Atomic Force Microscopy (AFM)-based Single-molecule Force Spectroscopy (SMFS) in Polymer Characterization
    Zhang, Wei
    Hou, Jue
    Li, Nan
    Zhang, Wen-ke
    ACTA POLYMERICA SINICA, 2021, 52 (11): : 1523 - 1546
  • [9] Novel polymer linkers for single molecule AFM force spectroscopy
    Tong, Zenghan
    Mikheikin, Andrey
    Krasnoslobodtsev, Alexey
    Lv, Zhengjian
    Lyubchenko, Yuri L.
    METHODS, 2013, 60 (02) : 161 - 168
  • [10] Improved Single Molecule Force Spectroscopy Using Micromachined Cantilevers
    Bull, Matthew S.
    Sullan, Ruby May A.
    Li, Hongbin
    Perkins, Thomas T.
    ACS NANO, 2014, 8 (05) : 4984 - 4995