Surface-engineered quantum dots for the labeling of hydrophobic microdomains in bacterial biofilms

被引:50
作者
Aldeek, Fadi [1 ,2 ]
Mustin, Christian [3 ]
Balan, Lavinia [4 ]
Roques-Carmes, Thibault [1 ]
Fontaine-Aupart, Marie-Pierre [5 ]
Schneider, Raphael [1 ]
机构
[1] Nancy Univ, CNRS, LRGP, F-54001 Nancy, France
[2] Nancy Univ, CNRS, LCPME, F-54506 Villers Les Nancy, France
[3] Nancy Univ, CNRS, LIMOS, F-54506 Vandoeuvre Les Nancy, France
[4] IS2M, LRC 7228, F-68093 Mulhouse, France
[5] Univ Paris Sud, ISMO, UMR 8214, F-91405 Orsay, France
关键词
Biofilm; ECM (extracellular matrix); Fluorescence; Hydrophilicity; Nanoparticle; Surface modification; FLUORESCENCE CORRELATION SPECTROSCOPY; EXTRACELLULAR POLYMERS; ACTIVATED-SLUDGE; CDSE; CDTE; PEPTIDES; PROBES; CELLS; EPS;
D O I
10.1016/j.biomaterials.2011.04.019
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Quantum dots (QDs) nanoprobes are emerging as alternatives to small-molecule fluorescent probes in biomedical technology. This paper reports an efficient and rapid method of producing highly dispersed and stable CdSe-core QDs with a hydrophobic gradient. Amphiphilic core/shell CdSe/ZnS QDs were prepared by ligand exchange at the surface of lipophilic CdSe/ZnS QDs using the dihydrolipoic acid (DHLA) dithiol ligand linked to Leucine or Phenylalanine aminoacids. Contact angle relaxations on a hydrophobic surface and surface tension measurements indicated that aqueous dispersions of CdSe/ZnS@DHLA-Leu or CdSe/ZnS@DHLA-Phe QDs exhibit increased hydrophobicity compared to CdSe-core QDs capped by the hydrophilic 3-mercaptopropionic acid (MPA) ligand. We found that the surface functional groups and the ligand density at the periphery of these QDs significantly dictated their interactions with a complex biological matrix called biofilm. Using fluorescence confocal microscopy and an autocorrelation function (semi-variogram), we demonstrated that MPA-capped QDs were homogeneously associated to the biopolymers, while amphiphilic CdSe/ZnS@DHLA-Leu or CdSe/ZnS@DHLA-Phe QDs were specifically confined allowing identification of hydrophobic microdomains of the biofilms. Results obtained clearly point out that the final destination of QDs in biofilms can properly be controlled by an appropriate design of surface ligands. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:5459 / 5470
页数:12
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