Thioflavin T Hydroxylation at Basic pH and Its Effect on Amyloid Fibril Detection

被引:97
作者
Fodera, Vito [1 ,2 ]
Groenning, Minna [3 ]
Vetri, Valeria [1 ,2 ]
Librizzi, Fabio [1 ]
Spagnolo, Salvatore [1 ]
Cornett, Claus [3 ]
Olsen, Lars [4 ]
van de Weert, Marco [3 ]
Leone, Maurizio [1 ,2 ]
机构
[1] Univ Palermo, Dipartimento Sci Fis & Astron, I-90123 Palermo, Italy
[2] CNR, Inst Biofis, I-90146 Palermo, Italy
[3] Univ Copenhagen, Dept Pharmaceut & Analyt Chem, Fac Pharmaceut Sci, DK-2100 Copenhagen O, Denmark
[4] Univ Copenhagen, Dept Med Chem, Fac Pharmaceut Sci, DK-2100 Copenhagen O, Denmark
关键词
D O I
10.1021/jp805560c
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 fluorescent dye thioflavin T (ThT) is commonly used for in situ amyloid fibril detection. In this work, we focused on the spectroscopic properties and chemical stability of ThT in aqueous solution as a function of pH, temperature, and dye concentration. A reversible hydroxylation process occurs in alkaline solutions, which was characterized using a combination of UV-vis absorption spectroscopy, proton NMR, and density functional theory (DFT). On the basis of these studies, we propose a chemical structure for the hydroxylated form. Finally, by means of fluorescence spectroscopy, ThT hydroxylation effects on in situ amyloid detection have been investigated, providing new insights on the efficiency of the ThT assay for quantitative fibril evaluation at basic pH.
引用
收藏
页码:15174 / 15181
页数:8
相关论文
共 57 条
[1]  
ALBEDINI A, 2005, BIOCHEMISTRY-US, V44, P16284
[2]   A NEW MIXING OF HARTREE-FOCK AND LOCAL DENSITY-FUNCTIONAL THEORIES [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (02) :1372-1377
[3]   DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE [J].
BECKE, AD .
JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) :5648-5652
[4]  
Brange J., 2000, PHARM FORMULATION DE
[5]   Effects of intermediates on aggregation of native bovine serum albumin [J].
Bulone, D ;
Martorana, V ;
San Biagio, PL .
BIOPHYSICAL CHEMISTRY, 2001, 91 (01) :61-69
[6]   Designing conditions for in vitro formation of amyloid protofilaments and fibrils [J].
Chiti, F ;
Webster, P ;
Taddei, N ;
Clark, A ;
Stefani, M ;
Ramponi, G ;
Dobson, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (07) :3590-3594
[7]   Studies of the aggregation of mutant proteins in vitro provide insights into the genetics of amyloid diseases [J].
Chiti, F ;
Calamai, M ;
Taddei, N ;
Stefani, M ;
Ramponi, G ;
Dobson, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 :16419-16426
[8]   FACTORS INFLUENCING THE PHOTOSENSITIZING PROPERTIES AND PHOTO-LUMINESCENCE OF THIOFLAVIN-T [J].
CUNDALL, RB ;
DAVIES, AK ;
MORRIS, PG ;
WILLIAMS, J .
JOURNAL OF PHOTOCHEMISTRY, 1981, 17 (3-4) :369-376
[9]   Protein misfolding, evolution and disease [J].
Dobson, CM .
TRENDS IN BIOCHEMICAL SCIENCES, 1999, 24 (09) :329-332
[10]   Principles of protein folding, misfolding and aggregation [J].
Dobson, CM .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2004, 15 (01) :3-16