Literature DB >> 19621878

Discovery of dermorphin-based affinity labels with subnanomolar affinity for mu opioid receptors.

Bhaswati Sinha1, Zhengyu Cao, Thomas F Murray, Jane V Aldrich.   

Abstract

A series of potent electrophilic affinity labels (IC(50) = 0.1-5 nM) containing either a bromoacetamide or isothiocyanate based on the mu opioid receptor (MOR) selective peptide dermorphin were prepared. All four analogues exhibited wash resistant inhibition of [(3)H]DAMGO binding at subnanomolar to nanomolar concentrations, suggesting that these analogues bind covalently to MOR. To our knowledge, these peptides are the highest affinity peptide-based affinity labels for MOR reported to date.

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Year:  2009        PMID: 19621878      PMCID: PMC2788677          DOI: 10.1021/jm9007592

Source DB:  PubMed          Journal:  J Med Chem        ISSN: 0022-2623            Impact factor:   7.446


  22 in total

1.  Affinity labeling of delta-opiate receptors using [D-Ala2,Leu5,Cys6]enkephalin. Covalent attachment via thiol-disulfide exchange.

Authors:  W D Bowen; S B Hellewell; M Kelemen; R Huey; D Stewart
Journal:  J Biol Chem       Date:  1987-10-05       Impact factor: 5.157

2.  Dermorphin-based potential affinity labels for mu-opioid receptors.

Authors:  H Choi; T F Murray; J V Aldrich
Journal:  J Pept Res       Date:  2003-01

3.  Primary structures and expression from cDNAs of rat opioid receptor delta- and mu-subtypes.

Authors:  K Fukuda; S Kato; K Mori; M Nishi; H Takeshima
Journal:  FEBS Lett       Date:  1993-08-02       Impact factor: 4.124

4.  Synthesis and evaluation of N,N-dialkyl enkephalin-based affinity labels for delta opioid receptors.

Authors:  D Y Maeda; J E Ishmael; T F Murray; J V Aldrich
Journal:  J Med Chem       Date:  2000-10-19       Impact factor: 7.446

5.  Determination of the amino acid residue involved in [3H]beta-funaltrexamine covalent binding in the cloned rat mu-opioid receptor.

Authors:  C Chen; J Yin; J K Riel; R L DesJarlais; L F Raveglia; J Zhu; L Y Liu-Chen
Journal:  J Biol Chem       Date:  1996-08-30       Impact factor: 5.157

6.  Synthesis and opioid activity of conformationally constrained dynorphin A analogues. 2. Conformational constraint in the "address" sequence.

Authors:  S Arttamangkul; J E Ishmael; T F Murray; D K Grandy; G E DeLander; B L Kieffer; J V Aldrich
Journal:  J Med Chem       Date:  1997-04-11       Impact factor: 7.446

7.  Molecular cloning and functional expression of a mu-opioid receptor from rat brain.

Authors:  Y Chen; A Mestek; J Liu; J A Hurley; L Yu
Journal:  Mol Pharmacol       Date:  1993-07       Impact factor: 4.436

8.  Discriminative affinity labelling of opioid receptors by enkephalin and morphiceptin analogues containing 3-nitro-2-pyridinesulphenyl-activated thiol residues.

Authors:  Y Shimohigashi; K Takada; H Sakamoto; H Matsumoto; T Yasunaga; M Kondo; M Ohno
Journal:  J Chromatogr       Date:  1992-04-24

9.  Characterization of irreversible binding of beta-funaltrexamine to the cloned rat mu opioid receptor.

Authors:  C Chen; J C Xue; J Zhu; Y W Chen; S Kunapuli; J Kim de Riel; L Yu; L Y Liu-Chen
Journal:  J Biol Chem       Date:  1995-07-28       Impact factor: 5.157

10.  Structure-activity relationships of novel cyclic alpha-MSH/beta-MSH hybrid analogues that lead to potent and selective ligands for the human MC3R and human MC5R.

Authors:  Preeti Balse-Srinivasan; Paolo Grieco; Minying Cai; Dev Trivedi; Victor J Hruby
Journal:  J Med Chem       Date:  2003-08-14       Impact factor: 7.446

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  1 in total

1.  Solution-phase-peptide synthesis via the group-assisted purification (GAP) chemistry without using chromatography and recrystallization.

Authors:  Jianbin Wu; Guanghui An; Siqi Lin; Jianbo Xie; Wei Zhou; Hao Sun; Yi Pan; Guigen Li
Journal:  Chem Commun (Camb)       Date:  2014-02-07       Impact factor: 6.222

  1 in total

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