High Affinity Fluorescent Ligands for the Estrogen Receptor

被引:18
作者
Abendroth, Frank [1 ]
Solleder, Marthe [2 ]
Mangoldt, Dorothea [3 ]
Welker, Pia [3 ]
Licha, Kai [3 ]
Weber, Marcus [2 ]
Seitz, Oliver [1 ]
机构
[1] Humboldt Univ, Dept Chem, D-12489 Berlin, Germany
[2] Zuse Inst Berlin, D-14195 Berlin, Germany
[3] Mivenion GmbH, D-10115 Berlin, Germany
关键词
Click chemistry; Hormones; Fluorescence; Fluorescent probes; Receptor-ligand interactions; Molecular simulation; Cyanines; BINDING; RECOGNITION; ANTAGONISM; ESTRADIOL; ASSAY;
D O I
10.1002/ejoc.201403489
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Fluorescent binders of the estrogen receptor (ER) are used in binding assays and in detection or imaging studies. However, fluorescence labelling of ER ligands usually leads to substantial decreases in binding affinity. In this study, we describe the development of high affinity fluorescent ER ligands. Cyanine dyes of the MiDye series were directly attached to the SERMs 4-hydroxytamoxifen (OHT) and raloxifene (Ral); linkers were deliberately omitted. This approach yielded conjugates with ER binding affinities superior to the natural ligand estradiol. The OHT- and Ral-MiDye conjugates emitted in the 600-800 nm range. First round staining experiments showed that the conjugates, but not the dyes alone, accumulate in cells expressing estrogen-binding receptors.
引用
收藏
页码:2157 / 2166
页数:10
相关论文
共 25 条
[1]   DNA-Controlled Bivalent Presentation of Ligands for the Estrogen Receptor [J].
Abendroth, Frank ;
Bujotzek, Alexander ;
Shan, Min ;
Haag, Rainer ;
Weber, Marcus ;
Seitz, Oliver .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (37) :8592-8596
[2]   Molecular basis of agonism and antagonism in the oestrogen receptor [J].
Brzozowski, AM ;
Pike, ACW ;
Dauter, Z ;
Hubbard, RE ;
Bonn, T ;
Engstrom, O ;
Ohman, L ;
Greene, GL ;
Gustafsson, JA ;
Carlquist, M .
NATURE, 1997, 389 (6652) :753-758
[3]  
Case DA., 2014, AMBER14
[4]   A water-soluble perylene dye functionalised with a 17β-estradiol: a new fluorescent tool for steroid hormones [J].
Cespedes-Guirao, Francisco J. ;
Ropero, Ana B. ;
Font-Sanchis, Enrique ;
Nadal, Angel ;
Fernandez-Lazaro, Fernando ;
Sastre-Santos, Angela .
CHEMICAL COMMUNICATIONS, 2011, 47 (29) :8307-8309
[5]   International Union of Pharmacology.: LXIV.: Estrogen receptors [J].
Dahlman-Wright, Karin ;
Cavailles, Vincent ;
Fuqua, Suzanne A. ;
Jordan, V. Craig ;
Katzenellenbogen, John A. ;
Korach, Kenneth S. ;
Maggi, Adriana ;
Muramatsu, Masami ;
Parker, Malcolm G. ;
Gustafsson, Jan-Ake .
PHARMACOLOGICAL REVIEWS, 2006, 58 (04) :773-781
[6]   Hands-off Linear Interaction Energy Approach to Binding Mode and Affinity Estimation of Estrogens [J].
Durmaz, Vedat ;
Schmidt, Sebastian ;
Sabri, Peggy ;
Piechotta, Christian ;
Weber, Marcus .
JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2013, 53 (10) :2681-2688
[7]   GROMACS 4: Algorithms for highly efficient, load-balanced, and scalable molecular simulation [J].
Hess, Berk ;
Kutzner, Carsten ;
van der Spoel, David ;
Lindahl, Erik .
JOURNAL OF CHEMICAL THEORY AND COMPUTATION, 2008, 4 (03) :435-447
[8]   Development of an improved four-site water model for biomolecular simulations: TIP4P-Ew [J].
Horn, HW ;
Swope, WC ;
Pitera, JW ;
Madura, JD ;
Dick, TJ ;
Hura, GL ;
Head-Gordon, T .
JOURNAL OF CHEMICAL PHYSICS, 2004, 120 (20) :9665-9678
[9]   DONOR-ACCEPTOR TETRAHYDROCHRYSENES, INHERENTLY FLUORESCENT, HIGH-AFFINITY LIGANDS FOR THE ESTROGEN-RECEPTOR - BINDING AND FLUORESCENCE CHARACTERISTICS AND FLUOROMETRIC ASSAY OF RECEPTOR [J].
HWANG, KJ ;
CARLSON, KE ;
ANSTEAD, GM ;
KATZENELLENBOGEN, JA .
BIOCHEMISTRY, 1992, 31 (46) :11536-11545
[10]   Nonclassical SNAPFL Analogue as a Cy5 Resonance Energy Transfer Partner [J].
Kim, Sung Hoon ;
Gunther, Jillian R. ;
Katzenellenbogen, John A. .
ORGANIC LETTERS, 2008, 10 (21) :4931-4934