Nanoparticle energy transfer on the cell surface

被引:22
作者
Bene, L [1 ]
Szentesi, G
Mátyus, L
Gáspár, R
Damjanovich, S
机构
[1] Univ Debrecen, Res Ctr Mol Med, Med & Hlth Sci Ctr, Dept Biophys & Cell Biol, H-4012 Debrecen, Hungary
[2] Hungarian Acad Sci, Cell Biophys Res Grp, H-4012 Debrecen, Hungary
关键词
plasmon resonance; 90 light scattering; fluorescence energy transfer; photobleaching; receptor clustering; MHCI and MHCII antigens; transferrin receptor; CD45;
D O I
10.1002/jmr.730
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
Membrane topology of receptors plays an important role in shaping transmembrane signalling of cells. Among the methods used for characterizing receptor clusters, fluorescence resonance energy transfer between a donor and acceptor fluorophore plays a unique role based on its capability of detecting molecular level (2-10 nm) proximities of receptors in physiological conditions. Recent development of biotechnology has made possible the usage of colloidal gold particles in a large size range for specific labelling of cells for the purposes of electron microscopy. However, by combining metal and fluorophore labelling or cells, the versatility of metal-fluorophore interactions opens the way for new applications by detecting the presence of the metal particles by the methods of fluorescence spectroscopy. An outstanding feature of the metal nanoparticle-fluorophore interaction is that the metal particle can enhance spontaneous emission of the fluorophore in a distance-dependent fashion, in an interaction range esentially determined by the size of the nanoparticle. In our work enhanced fluorescence of rhodamine and cyanine dyes was observed in the vicinity of immunogold nanoparticles on the surface of JY cells in a flow cytometer. The dyes and the immunogold were targetted to the cell surface receptors MHCI, MHCII, transferrin receptor and CD45 by monoclonal antibodies. The fluorescence enhancement was sensitive to the wavelength of the exciting light, the size and amount of surface bound gold beads, as well as the fluorophore-nanoparticle distance. The intensity of 90 degrees scattering of the incident light beam was enhanced by the immunogold in a concentration and size-dependent fashion. The 90 degrees light scattering varied with the wavelength of the incident light in a manner characteristic to gold nanoparticles of the applied sizes. A reduction in photobleaching time constant of the cyanine dye was observed in the vicinity of gold particles in a digital imaging microscope. Modulations of 90 degrees light scattering intensity and photobleaching time constant indicate the role of the local field in the fluorescence enhancement. A mathematical simulation based on the electrodynamic theory of fluorescence enhancement showed a consistency between the measured enhancement values, the inter-epitope distances and the quantum yields. The feasibility of realizing proximity sensors operating at distance ranges larger than that of the conventional Forster transfer is demonstrated on the surface of living cells. Copyright (c) 2004 John Wiley& Sons, Ltd.
引用
收藏
页码:236 / 253
页数:18
相关论文
共 70 条
[1]  
[Anonymous], 1994, MOBILITY PROXIMITY B
[2]   INF-γ rearranges membrane topography of MHC-I and ICAM-1 in colon carcinoma cells [J].
Bacsó, Z ;
Bene, L ;
Damjanovich, L ;
Damjanovich, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 290 (02) :635-640
[3]   PRODUCTION OF MONOCLONAL ANTIBODIES TO GROUP-A ERYTHROCYTES, HLA AND OTHER HUMAN CELL-SURFACE ANTIGENS - NEW TOOLS FOR GENETIC-ANALYSIS [J].
BARNSTABLE, CJ ;
BODMER, WF ;
BROWN, G ;
GALFRE, G ;
MILSTEIN, C ;
WILLIAMS, AF ;
ZIEGLER, A .
CELL, 1978, 14 (01) :9-20
[4]  
Bauer G, 1999, MIKROCHIM ACTA, V131, P107, DOI 10.1007/s006040050015
[5]  
Bene L, 1997, CYTOMETRY, V27, P353, DOI 10.1002/(SICI)1097-0320(19970401)27:4<353::AID-CYTO6>3.3.CO
[6]  
2-Q
[7]   LATERAL ORGANIZATION OF THE ICAM-1 MOLECULE AT THE SURFACE OF HUMAN LYMPHOBLASTS - A POSSIBLE MODEL FOR ITS CODISTRIBUTION WITH THE IL-2 RECEPTOR, CLASS-I AND CLASS-II HLA MOLECULES [J].
BENE, L ;
BALAZS, M ;
MATKO, J ;
MOST, J ;
DIERICH, MP ;
SZOLLOSI, J ;
DAMJANOVICH, S .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1994, 24 (09) :2115-2123
[8]   FLOW CYTOMETRIC ANALYSIS OF IMMUNOGOLD CELL-SURFACE LABEL [J].
BOHMER, RM ;
KING, NJC .
CYTOMETRY, 1984, 5 (05) :543-546
[9]  
Born M, 2003, PRINCIPLES OPTICS EL, P735
[10]   LIFETIME OF AN EMITTING MOLECULE NEAR A PARTIALLY REFLECTING SURFACE [J].
CHANCE, RR ;
PROCK, A ;
SILBEY, R .
JOURNAL OF CHEMICAL PHYSICS, 1974, 60 (07) :2744-2748