Functionalization of probe tips and supports for single-molecule recognition force Microscopy

被引:60
作者
Ebner, Andreas
Wildling, Linda
Zhu, Rong
Rankl, Christian
Haselgruebler, Thomas
Hinterdorfer, Peter
Gruber, Hermann J.
机构
来源
STM AND AFM STUDIES ON (BIO)MOLECULAR SYSTEMS: UNRAVELLING THE NANOWORLD | 2008年 / 285卷
基金
奥地利科学基金会;
关键词
D O I
10.1007/128_2007_24
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The measuring tip of a force microscope can be converted into a monomolecular sensor if one or few "ligand" molecules are attached to the apex of the tip while maintaining ligand function. Functionalized tips are used to study fine details of receptor-ligand interaction by force spectroscopy or to map cognate "receptor" molecules on the sample surface. The receptor (or target) molecules can be present on the surface of a biological specimen; alternatively, soluble target molecules must be immobilized on ultraflat supports. This review describes the methods of tip functionalization, as well as target molecule immobilization. Silicon nitride tips, silicon chips, and mica have usually been functionalized in three steps: (1) aminofunctionalization, (2) crosslinker attachment, and (3) ligand/receptor coupling, whereby numerous crosslinkers are available to couple widely different ligand molecules. Gold-covered tips and/or supports have usually been coated with a self-assembled monolayer, on top of which the ligand/receptor molecule has been coupled either directly or via a crosslinker molecule. Apart from these general strategies, many simplified methods have been used for tip and/or support functionalization, even single-step methods such as adsorption or chemisorption being very efficient under suitable circumstances. All methods are described with the same explicitness and critical parameters are discussed. In conclusion, this review should help to find suitable methods for specific problems of tip and support functionalization.
引用
收藏
页码:29 / 76
页数:48
相关论文
共 196 条
  • [1] Analysis of force curves obtained on the live cell membrane using chemically modified AFM probes
    Afrin, R
    Yamada, T
    Ikai, A
    [J]. ULTRAMICROSCOPY, 2004, 100 (3-4) : 187 - 195
  • [2] Detection of antigen-antibody binding events with the atomic force microscope
    Allen, S
    Chen, XY
    Davies, J
    Davies, MC
    Dawkes, AC
    Edwards, JC
    Roberts, CJ
    Sefton, J
    Tendler, SJB
    Williams, PM
    [J]. BIOCHEMISTRY, 1997, 36 (24) : 7457 - 7463
  • [3] Elasticity and adhesion force mapping reveals real-time clustering of growth factor receptors and associated changes in local cellular rheological properties
    Almqvist, N
    Bhatia, R
    Primbs, G
    Desai, N
    Banerjee, S
    Lal, R
    [J]. BIOPHYSICAL JOURNAL, 2004, 86 (03) : 1753 - 1762
  • [4] ANDRADE J D, 1992, Clinical Materials, V11, P67, DOI 10.1016/0267-6605(92)90031-N
  • [5] β-cyclodextrin host-guest complexes probed under thermodynamic equilibrium:: Thermodynamics and AFM force spectroscopy
    Auletta, T
    de Jong, MR
    Mulder, A
    van Veggel, FCJM
    Huskens, J
    Reinhoudt, DN
    Zou, S
    Zapotoczny, S
    Schönherr, H
    Vancso, GJ
    Kuipers, L
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (05) : 1577 - 1584
  • [6] Comparison of antibody-antigen interactions on collagen measured by conventional immunological techniques and atomic force microscopy
    Avci, R
    Schweitzer, M
    Boyd, RD
    Wittmeyer, J
    Steele, A
    Toporski, J
    Beech, W
    Arce, FT
    Spangler, B
    Cole, KM
    McKay, DS
    [J]. LANGMUIR, 2004, 20 (25) : 11053 - 11063
  • [7] Cadherin interaction probed by atomic force microscopy
    Baumgartner, W
    Hinterdorfer, P
    Ness, W
    Raab, A
    Vestweber, D
    Schindler, H
    Drenckhahn, D
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (08) : 4005 - 4010
  • [8] Baumgartner W, 2003, J NEUROSCI, V23, P11008
  • [9] Baumgartner W., 2000, Single Molecules, V1, P119, DOI 10.1002/1438-5171(200006)1:2<119::AID-SIMO119>3.0.CO
  • [10] 2-K