Oligoproline helices as structurally defined scaffolds for oligomeric G protein-coupled receptor ligands

被引:24
作者
Bonger, Kimberly M. [1 ]
Kapoerchan, Varsha V. [1 ]
Grotenbreg, Gijsbert M. [1 ]
van Koppen, Chris J. [2 ]
Timmers, C. Marco [3 ]
van der Marel, Gijsbert A. [1 ]
Overkleeft, Herman S. [1 ]
机构
[1] Leiden Univ, Leiden Inst Chem, Gorlaeus Labs, Dept Bioorgan Synth, NL-2300 RA Leiden, Netherlands
[2] Schering Plough Res Inst, Dept Mol Pharmacol, NL-5340 BH Oss, Netherlands
[3] Schering Plough Res Inst, Dept Med Chem, NL-5340 BH Oss, Netherlands
关键词
POLYPROLINE-II STRUCTURE; BIVALENT LIGANDS; CONFORMATION; STABILITY; AGONISTS; LENGTH;
D O I
10.1039/b923556f
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Oligoprolines (OPs) are used as rigid backbone scaffolds for the design of oligomeric ligands that target specific G protein-coupled receptors. The OPs were designed to vary in length, the position and number of the ligand-functionalized residues incorporated. For all synthesized compounds a typical PP type II helix was evidenced by circular dichroism indicating that decoration of the helix with large ligands did not affect the helical conformation. Pharmacological evaluation revealed that oligomerization of an agonist with the use of an oligoproline scaffold showed an increase in potency when compared to the monomeric counterparts.
引用
收藏
页码:1881 / 1884
页数:4
相关论文
共 31 条
[21]   A 10-Å spectroscopic ruler applied to short polyprolines [J].
Sahoo, Harekrushna ;
Roccatano, Danilo ;
Hennig, Andreas ;
Nau, Werner M. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2007, 129 (31) :9762-9772
[22]   Conformation of the backbone in unfolded proteins [J].
Shi, Zhengshuang ;
Chen, Kang ;
Liu, Zhigang ;
Kallenbach, Neville R. .
CHEMICAL REVIEWS, 2006, 106 (05) :1877-1897
[23]   The follicle-stimulating hormone receptor: Biochemistry, molecular biology, physiology, and pathophysiology [J].
Simoni, M ;
Gromoll, J ;
Nieschlag, E .
ENDOCRINE REVIEWS, 1997, 18 (06) :739-773
[24]   The "azido gauche effect"-implications for the conformation of azidoprolines [J].
Sonntag, Louis-Sebastian ;
Schweizer, Sabine ;
Ochsenfeld, Christian ;
Wennemers, Helma .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2006, 128 (45) :14697-14703
[25]  
Stapley BJ, 1999, PROTEIN SCI, V8, P587
[26]   ENERGY TRANSFER - A SPECTROSCOPIC RULER [J].
STRYER, L ;
HAUGLAND, RP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1967, 58 (02) :719-&
[27]   Roles of G-protein-coupled receptor dimerization - From ontogeny to signalling regulation [J].
Terrillon, S ;
Bouvier, M .
EMBO REPORTS, 2004, 5 (01) :30-34
[28]   Induction of ovulation by a potent, orally active, low molecular weight agonist (Org 43553) of the luteinizing hormone receptor [J].
van de Lagemaat, R. ;
Timmers, C. M. ;
Kelder, J. ;
van Koppen, C. ;
Mosselman, S. ;
Hanssen, R. G. J. M. .
HUMAN REPRODUCTION, 2009, 24 (03) :640-648
[29]   A signaling-selective, nanomolar potent allosteric low molecular weight agonist for the human luteinizing hormone receptor [J].
van Koppen, Chris J. ;
Zaman, Guido J. R. ;
Timmers, C. Marco ;
Kelder, Jan ;
Mosselman, Sietse ;
van de Lagemaat, Ruud ;
Smit, Martin J. ;
Hanssen, Rob G. J. M. .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2008, 378 (05) :503-514
[30]  
van Straten NCR, 2002, CHEMBIOCHEM, V3, P1023, DOI 10.1002/1439-7633(20021004)3:10<1023::AID-CBIC1023>3.0.CO