Monitoring ligand-receptor interactions by photonic force microscopy

被引:19
作者
Jeney, Sylvia [1 ,2 ]
Mor, Flavio [2 ]
Koszali, Roland [3 ]
Forro, Laszlo [2 ]
Moy, Vincent T. [4 ]
机构
[1] Univ Basel, Biozentrum, ME Muller Inst Struct Biol, CH-4056 Basel, Switzerland
[2] Ecole Polytech Fed Lausanne, LPMC, CH-1015 Lausanne, Switzerland
[3] Univ Appl Sci Western Switzerland HEIG VD, IICT, CH-1401 Yverdon, Switzerland
[4] Univ Miami, Dept Physiol & Biophys, Miller Sch Med, Miami, FL 33136 USA
基金
瑞士国家科学基金会;
关键词
OPTICAL TWEEZERS; CATCH BONDS; STREPTAVIDIN; ADHESION; CELLS; MOLECULES; STRENGTH; DNA;
D O I
10.1088/0957-4484/21/25/255102
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We introduce a method for the acquisition of single molecule force measurements of ligand-receptor interactions using the photonic force microscope (PFM). Biotin-functionalized beads, manipulated with an optical trap, and a streptavidin-functionalized coverslip were used to measure the effect of different pulling forces on the lifetime of individual streptavidin-biotin complexes. By optimizing the design of the optical trap and selection of the appropriate bead size, pulling forces in excess of 50 pN were achieved. Based on the amplitude of three-dimensional (3D) thermal position fluctuations of the attached bead, we were able to select for a bead-coverslip interaction that was mediated by a single streptavidin-biotin complex. Moreover, the developed experimental system was greatly accelerated by automation of data acquisition and analysis. In force-dependent kinetic measurements carried out between streptavidin and biotin, we observed that the streptavidin-biotin complex exhibited properties of a catch bond, with the lifetime increasing tenfold when the pulling force increased from 10 to 20 pN. We also show that silica beads were more appropriate than polystyrene beads for the force measurements, as tethers, longer than 200 nm, could be extracted from polystyrene beads.
引用
收藏
页数:8
相关论文
共 50 条
  • [1] Single-molecule force spectroscopy: a method for quantitative analysis of ligand-receptor interactions
    Fuhrmann, Alexander
    Ros, Robert
    NANOMEDICINE, 2010, 5 (04) : 657 - 666
  • [2] Atomic force microscopy study of the effect of HER 2 antibody on EGF mediated ErbB ligand-receptor interaction
    Zhang, Xuejie
    Shi, Xiaoli
    Xu, Li
    Yuan, Jinghe
    Fang, Xiaohong
    NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2013, 9 (05) : 627 - 635
  • [3] Ligand dimerization programmed by hybridization to study multimeric ligand-receptor interactions
    Gorska, Katarzyna
    Beyrath, Julien
    Fournel, Sylvie
    Guichard, Gilles
    Winssinger, Nicolas
    CHEMICAL COMMUNICATIONS, 2010, 46 (41) : 7742 - 7744
  • [4] Exploiting Ligand-Protein Conjugates to Monitor Ligand-Receptor Interactions
    Haruki, Hirohito
    Gonzalez, Monica Rengifo
    Johnsson, Kai
    PLOS ONE, 2012, 7 (05):
  • [5] Colloidal probe microscopy of membrane-membrane interactions: From ligand-receptor recognition to fusion events
    Lorenz, Baerbel
    Keller, Rabea
    Sunnick, Eva
    Geil, Burkhard
    Janshoff, Andreas
    BIOPHYSICAL CHEMISTRY, 2010, 150 (1-3) : 54 - 63
  • [6] Influence of ligand-receptor interactions on force-extension behavior within the freely jointed chain model
    Radiom, Milad
    Borkovec, Michal
    PHYSICAL REVIEW E, 2017, 96 (06)
  • [7] Probing Ligand-Receptor Interaction in Living Cells Using Force Measurements With Optical Tweezers
    Riesenberg, Carolin
    Iriarte-Valdez, Christian Alejandro
    Becker, Annegret
    Dienerowitz, Maria
    Heisterkamp, Alexander
    Ngezahayo, Anaclet
    Torres-Mapa, Maria Leilani
    FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY, 2020, 8
  • [8] The quantity of ligand-receptor interactions between nanoparticles and target cells
    Schorr, Kathrin
    Beck, Sebastian
    Zimmer, Oliver
    Baumann, Felix
    Keller, Max
    Witzgall, Ralph
    Goepferich, Achim
    NANOSCALE HORIZONS, 2025, 10 (04) : 803 - 823
  • [9] Cellinker: a platform of ligand-receptor interactions for intercellular communication analysis
    Zhang, Yang
    Liu, Tianyuan
    Wang, Jing
    Zou, Bohao
    Li, Le
    Yao, Linhui
    Chen, Kechen
    Ning, Lin
    Wu, Bingyi
    Zhao, Xiaoyang
    Wang, Dong
    BIOINFORMATICS, 2021, 37 (14) : 2025 - 2032
  • [10] Bond formation kinetics affects self-assembly directed by ligand-receptor interactions
    Bachmann, Stephan Jan
    Petitzon, Marius
    Mognetti, Bortolo Matteo
    SOFT MATTER, 2016, 12 (47) : 9585 - 9592