Fluorescence probe techniques to monitor protein adsorption-induced conformation changes on biodegradable polymers

被引:39
作者
Benesch, Johan
Hungerford, Graham
Suhling, Klaus
Tregidgo, Carolyn
Mano, Joao F.
Reis, Rui L.
机构
[1] Univ Minho, Res Grp 3B, Dept Polymer Engn, P-4710057 Braga, Portugal
[2] IBB, PT Govt Associated Lab, Braga, Portugal
[3] Univ Minho, Dept Phys, P-4710057 Braga, Portugal
[4] Kings Coll London, Dept Phys, London WC2R 2LS, England
关键词
fluorescence; anisotropy; time resolved; albumin; protein conformation; fluorescence lifetime imaging; synchronous scan; tryptophan; nile red; fluorescein isothiocyanate;
D O I
10.1016/j.jcis.2007.03.016
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The study of protein adsorption and any associated conformational changes on interaction with biomaterials is of great importance in the area of implants and tissue constructs. This study aimed to evaluate some fluorescent techniques to probe protein conformation on a selection of biodegradable polymers currently under investigation for biomedical applications. Because of the fluorescence emanating from the polymers, the use of monitoring intrinsic protein fluorescence was precluded. A highly solvatochromic fluorescent dye, Nile red, and a well-known protein label, fluorescein isothiocyanate, were employed to study the adsorption of serum albumin to polycaprolactone and to some extent also to two starch-containing polymer blends (SPCL and SEVA-C). A variety of fluorescence techniques, steady state, time resolved, and imaging were employed. Nile red was found to each from the protein, while fluorescein isothiocyanate proved useful in elucidating a conformational change in the protein and the observation of protein aggregates adsorbed to the polymer surface. These effects were seen by making use of the phenomenon of energy migration between the fluorescent tags to monitor interprobe distance and the use of fluorescence lifetime imaging to ascertain the surface packing of the protein on polymer. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:193 / 200
页数:8
相关论文
共 61 条
[1]   IMMUNOCHEMICAL AND SPECTROSCOPIC CHARACTERIZATION OF 2 FLUORESCEIN 5'-ISOTHIOCYANATE LABELING SITES ON NA+,K+-ATPASE [J].
ABBOTT, AJ ;
AMLER, E ;
BALL, WJ .
BIOCHEMISTRY, 1991, 30 (06) :1692-1701
[2]   Single molecule fluorescence studies of surface-adsorbed fibronectin [J].
Antia, M ;
Islas, LD ;
Boness, DA ;
Baneyx, G ;
Vogel, V .
BIOMATERIALS, 2006, 27 (05) :679-690
[3]  
ARBELOA I.L. P., 1981, J CHEM SOC FARAD T 2, V77, P1725
[4]   DIMERIC AND TRIMERIC STATES OF THE FLUORESCEIN DIANION .2. EFFECTS ON FLUORESCENCE CHARACTERISTICS [J].
ARBELOA, IL .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS II, 1981, 77 :1735-1742
[5]   Structural changes of fibronectin adsorbed to model surfaces probed by fluorescence resonance energy transfer [J].
Baugh, L ;
Vogel, V .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2004, 69A (03) :525-534
[6]   ADSORPTION OF MONOCLONAL IGGS AND THEIR F(AB')(2) FRAGMENTS ONTO POLYMERIC SURFACES [J].
BUIJS, J ;
LICHTENBELT, JWT ;
NORDE, W ;
LYKLEMA, J .
COLLOIDS AND SURFACES B-BIOINTERFACES, 1995, 5 (1-2) :11-23
[7]   MECHANISM OF FLUORESCENCE CONCENTRATION QUENCHING OF CARBOXYFLUORESCEIN IN LIPOSOMES - ENERGY-TRANSFER TO NONFLUORESCENT DIMERS [J].
CHEN, RF ;
KNUTSON, JR .
ANALYTICAL BIOCHEMISTRY, 1988, 172 (01) :61-77
[8]  
Davis PW, 1996, METHOD MOL CELL BIOL, V6, P23
[9]  
Deka C, 1996, CYTOMETRY, V25, P271, DOI 10.1002/(SICI)1097-0320(19961101)25:3<271::AID-CYTO8>3.0.CO
[10]  
2-I