Photoaffinity labeling of the human substance P (neurokinin-1) receptor with [3H2]azido-CP-96,345, a photoreactive derivative of a nonpeptide antagonist.

Abstract:

:An azido derivative of [3H2](2S, 3S)-cis-2-(diphenylmethyl)-N-((2-methoxyphenyl) methyl)-1-azabicyclo[2.2.2]octon-3-amine (CP-96,345), a potent nonpeptide antagonist of the substance P (SP) (neurokinin-1) receptor, was synthesized and shown to have an affinity for the human SP receptor similar to that of the parent compound, CP-96,345. When Chinese hamster ovary cells expressing the human SP receptor were photolabeled with this compound and analyzed with the use of sodium dodecyl sulfate-polyacrylamide gel electrophoresis and fluorography, several radioactive bands were observed, including a major band centered at molecular mass 80 kDa, the expected value for the SP receptor expressed in Chinese hamster ovary cells. Only the labeling of the 80-kDa protein was specific: nonradiolabeled CP-96,345 but not its optical enantiomer, CP-96,344 was a potent inhibitor of photoincorporation. SP prevented photolabeling only at concentrations higher than expected from its binding affinity but similar to those shown in a competition binding assay to displace radioiodinated analogue of CP-96,345. Antiserum generated against a synthetic peptide corresponding to the carboxyl terminus of the human SP receptor immunoprecipitated only the 80-kDa photoaffinity labeled protein, confirming that it is the human SP receptor. Interestingly, a second antiserum that was generated against the third extracellular loop of the G protein-coupled receptor no longer immunoprecipitated the receptor when covalently labeled with [3H2]azido-CP-96,345. This result indicates either that attachment of the antagonist modified the antigenic region directly, suggesting involvement of this domain in the binding of CP-96,345, or that the loss of recognition by the antiserum is secondary to a change in conformation induced by the covalent attachment of the antagonist at a different site.

journal_name

Mol Pharmacol

journal_title

Molecular pharmacology

authors

MacDonald D,Silberman SC,Lowe JA 3rd,Drozda SE,Leeman SE,Boyd ND

subject

Has Abstract

pub_date

1996-05-01 00:00:00

pages

808-13

issue

5

eissn

0026-895X

issn

1521-0111

journal_volume

49

pub_type

杂志文章
  • Mpl ligand increases P2Y1 receptor gene expression in megakaryocytes with no concomitant change in platelet response to ADP.

    abstract::The P2Y(1) receptor is responsible for the initiation of platelet aggregation in response to ADP and plays a key role in thrombosis. Although this receptor is expressed early in the platelet lineage, the regulation of its expression during megakaryocyte differentiation is unknown. In the mouse megakaryocytic cell line...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.60.5.1112

    authors: Hechler B,Toselli P,Ravanat C,Gachet C,Ravid K

    更新日期:2001-11-01 00:00:00

  • Histidine residues 912 and 913 in protein associated with Myc are necessary for the inhibition of adenylyl cyclase activity.

    abstract::We reported previously that protein associated with Myc (PAM) interacts with the C2 domain of type V adenylyl cyclase (ACV-C2) and that purified PAM is a potent inhibitor of Galphas-stimulated ACV activity (J Biol Chem 276:47583-47589, 2001). The present study was conducted to identify the region in PAM that inhibits ...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.104.005355

    authors: Gao X,Patel TB

    更新日期:2005-01-01 00:00:00

  • Constitutively active mutants of the histamine H1 receptor suggest a conserved hydrophobic asparagine-cage that constrains the activation of class A G protein-coupled receptors.

    abstract::The aim of this study was to create and characterize constitutively active mutant (CAM) histamine H(1) receptors (H(1)R) using random mutagenesis methods to further investigate the activation process of the rhodopsin-like family of G protein-coupled receptors (GPCRs). This approach identified position 6.40 in TM 6 as ...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.107.038547

    authors: Bakker RA,Jongejan A,Sansuk K,Hacksell U,Timmerman H,Brann MR,Weiner DM,Pardo L,Leurs R

    更新日期:2008-01-01 00:00:00

  • Photoaffinity labeling and purification of ZG-16p, a high-affinity dihydropyridine binding protein of rat pancreatic zymogen granule membranes that regulates a K(+)-selective conductance.

    abstract::In rat pancreatic zymogen granules (ZG), an ATP-sensitive K(+) conductance and a Cl(-) conductance have been characterized that are inversely regulated by an approximately 65-kDa multidrug resistance P-glycoprotein (mdr1) gene product. In search of a label for purification of this protein, we found that the dihydropyr...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Braun M,Thévenod F

    更新日期:2000-02-01 00:00:00

  • The low-potency, voltage-dependent HERG blocker propafenone--molecular determinants and drug trapping.

    abstract::The molecular determinants of high-affinity human ether-a-go-go-related gene (HERG) potassium channel blockade by methanesulfonanilides include two aromatic residues (Phe656 and Tyr652) on the inner helices (S6) and residues on the pore helices that face into the inner cavity, but determinants for lower-affinity HERG ...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.104.001743

    authors: Witchel HJ,Dempsey CE,Sessions RB,Perry M,Milnes JT,Hancox JC,Mitcheson JS

    更新日期:2004-11-01 00:00:00

  • Celecoxib inhibits interleukin-12 alphabeta and beta2 folding and secretion by a novel COX2-independent mechanism involving chaperones of the endoplasmic reticulum.

    abstract::Celecoxib (CE) is a nonsteroidal anti-inflammatory drug (NSAID) that is a specific inhibitor of cyclooxygenase 2 (COX2). It is indicated for a variety of chronic inflammatory conditions, including rheumatoid arthritis. Over the last few years, adverse cardiovascular effects and increased risk for heart attacks have be...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.105.020669

    authors: Alloza I,Baxter A,Chen Q,Matthiesen R,Vandenbroeck K

    更新日期:2006-05-01 00:00:00

  • Glucocorticoid-induced tumor necrosis factor receptor-related (GITR)-Fc fusion protein inhibits GITR triggering and protects from the inflammatory response after spinal cord injury.

    abstract::Glucocorticoid-induced tumor necrosis factor receptor-related (GITR) protein is a costimulatory molecule that plays a role in inflammation so that GITR-Fc fusion protein can exert an anti-inflammatory effect. To investigate the mechanism by which GITR-Fc exerts its effects, we first used GITR knock-out (GITR(-/-)) mic...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.107.044354

    authors: Nocentini G,Cuzzocrea S,Genovese T,Bianchini R,Mazzon E,Ronchetti S,Esposito E,Rosanna DP,Bramanti P,Riccardi C

    更新日期:2008-06-01 00:00:00

  • Tricyclic antidepressants and dextromethorphan bind with higher affinity to the phencyclidine receptor in the absence of magnesium and L-glutamate.

    abstract::Recent studies from our laboratory have provided evidence that multiple states of the phencyclidine (PCP) receptor exist. In addition, several compounds such as PCP and the novel anticonvulsant MK-801 were found to inhibit binding more potently in the presence of Mg2+ and L-glutamate (L-GLU) than when these agents wer...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Sills MA,Loo PS

    更新日期:1989-07-01 00:00:00

  • Down-regulation of STAT5b transcriptional activity by ligand-activated peroxisome proliferator-activated receptor (PPAR) alpha and PPARgamma.

    abstract::The nuclear receptor peroxisome proliferator-activated receptor (PPAR) is activated by a diverse group of acidic ligands, including many peroxisome proliferator chemicals present in the environment. Janus tyrosine kinase-signal transducer and activator of transcription (JAK-STAT) signaling is activated by multiple cyt...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.64.2.355

    authors: Shipley JM,Waxman DJ

    更新日期:2003-08-01 00:00:00

  • Pharmacological characterization of the cloned kappa-, delta-, and mu-opioid receptors.

    abstract::Opioid drugs, such as morphine, and the endogenous opioid peptides, namely the enkephalins, endorphins, and dynorphins, exert a wide spectrum of physiological and behavioral effects, including effects on pain perception, mood, motor control, and autonomic functions. These effects are mediated via membrane-bound recept...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Raynor K,Kong H,Chen Y,Yasuda K,Yu L,Bell GI,Reisine T

    更新日期:1994-02-01 00:00:00

  • CYP2C8 Is a Novel Target of Peroxisome Proliferator-Activated Receptor α in Human Liver.

    abstract::Human cytochrome P450 (CYP) 2C enzymes metabolize ∼30% of clinically prescribed drugs and various environmental chemicals. CYP2C8, an important member of this subfamily, metabolizes the anticancer drug paclitaxel, certain antidiabetic drugs, and endogenous substrates, including arachidonic acid, to physiologically act...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.115.100255

    authors: Makia NL,Goldstein JA

    更新日期:2016-01-01 00:00:00

  • Coupling efficiencies of human alpha 1-adrenergic receptor subtypes: titration of receptor density and responsiveness with inducible and repressible expression vectors.

    abstract::We compared the efficiencies with which human alpha 1-adrenergic receptor (AR) subtypes activate inositol phosphate (InsP) formation and increase intracellular Ca2+ in transfected cell lines. Expression of human alpha 1a-, alpha 1b-, and alpha 1d-AR cDNAs under the repressible control of anhydrotetracycline in human e...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Theroux TL,Esbenshade TA,Peavy RD,Minneman KP

    更新日期:1996-11-01 00:00:00

  • Transcriptional induction of hepatic NADPH: cytochrome P450 oxidoreductase by thyroid hormone.

    abstract::Studies were carried out to elucidate the mechanism whereby thyroid hormone (T3) induces NADPH:cytochrome P450 oxidoreductase (P450R) mRNA in rat liver in vivo. Northern blot analysis revealed that T3 treatment increases unspliced liver nuclear P450R RNA 4-fold within 8 h and that this induction precedes the induction...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.59.5.987

    authors: Li HC,Liu D,Waxman DJ

    更新日期:2001-05-01 00:00:00

  • Inactivation of multiple hepatic cytochrome P-450 isozymes in rats by allylisopropylacetamide: mechanistic implications.

    abstract::In vivo administration of the porphyrogenic agent allylisopropylacetamide (AIA) to phenobarbital-pretreated rats results in marked loss of hepatic cytochrome P-450 content. Using isozyme-selective functional markers, we now show that such loss reflects inactivation of several phenobarbital-inducible and constitutive i...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Bornheim LM,Underwood MC,Caldera P,Rettie AE,Trager WF,Wrighton SA,Correia MA

    更新日期:1987-08-01 00:00:00

  • Fluorescence resonance energy transfer analysis of alpha 2a-adrenergic receptor activation reveals distinct agonist-specific conformational changes.

    abstract::Several lines of evidence suggest that G-protein-coupled receptors can adopt different active conformations, but their direct demonstration in intact cells is still missing. Using a fluorescence resonance energy transfer (FRET)-based approach we studied conformational changes in alpha(2A)-adrenergic receptors in intac...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.108.052399

    authors: Zürn A,Zabel U,Vilardaga JP,Schindelin H,Lohse MJ,Hoffmann C

    更新日期:2009-03-01 00:00:00

  • The antiallergic mast cell stabilizers lodoxamide and bufrolin as the first high and equipotent agonists of human and rat GPR35.

    abstract::Lack of high potency agonists has restricted analysis of the G protein-coupled receptor GPR35. Moreover, marked variation in potency and/or affinity of current ligands between human and rodent orthologs of GPR35 has limited their productive use in rodent models of physiology. Based on the reported modest potency of th...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.113.089482

    authors: MacKenzie AE,Caltabiano G,Kent TC,Jenkins L,McCallum JE,Hudson BD,Nicklin SA,Fawcett L,Markwick R,Charlton SJ,Milligan G

    更新日期:2014-01-01 00:00:00

  • Characterization of human lung microsomal cytochrome P-450 1A1 and its role in the oxidation of chemical carcinogens.

    abstract::Rat and human lung microsomal cytochrome P-450 (P-450) enzymes have been characterized with regard to their catalytic activities towards several xenobiotic chemicals, including procarcinogens, in different microsomal preparations. Rat lung microsomal P-450s were more active than the human P-450s in catalyzing most of ...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Shimada T,Yun CH,Yamazaki H,Gautier JC,Beaune PH,Guengerich FP

    更新日期:1992-05-01 00:00:00

  • Geranylgeranylacetone protects membranes against nonsteroidal anti-inflammatory drugs.

    abstract::Direct gastric mucosal cell damage mediated by nonsteroidal anti-inflammatory drugs (NSAIDs) is involved in the formation of NSAID-induced gastric lesions. We recently suggested that this direct cytotoxicity of NSAIDs is caused by their membrane-permeabilization activity. Geranylgeranylacetone (GGA), a clinically used...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.105.015784

    authors: Ushijima H,Tanaka K,Takeda M,Katsu T,Mima S,Mizushima T

    更新日期:2005-10-01 00:00:00

  • Voltage-Independent Inhibition of the Tetrodotoxin-Sensitive Sodium Currents by Oxotremorine and Angiotensin II in Rat Sympathetic Neurons.

    abstract::Tetrodotoxin-sensitive Na(+) currents have been extensively studied because they play a major role in neuronal firing and bursting. In this study, we showed that voltage-dependent Na(+) currents are regulated in a slow manner by oxotremorine (oxo-M) and angiotensin II in rat sympathetic neurons. We found that these cu...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.115.101931

    authors: Puente EI,De la Cruz L,Arenas I,Elias-Viñas D,Garcia DE

    更新日期:2016-04-01 00:00:00

  • Mutations in the main cytoplasmic loop of the GABA(A) receptor α4 and δ subunits have opposite effects on surface expression.

    abstract::We examined the role of putative trafficking sequences in two GABA(A) receptor subunits: α4 and δ. These subunits assemble with a β subunit to form a subtype of GABA(A) receptor involved in generating the "tonic" outward current. Both α4 and δ subunits contain dibasic retention motifs in homologous positions. When bas...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.114.092791

    authors: Bracamontes JR,Li P,Akk G,Steinbach JH

    更新日期:2014-07-01 00:00:00

  • Ca2+-mediated neuronal death in rat brain neuronal cultures by veratridine: protection by flunarizine.

    abstract::Neuronal cell degeneration was studied in vitro in primary rat brain neuronal cultures grown in serum-free, chemically defined, CDM R12 medium, by measuring lactate dehydrogenase (LDH) released in the culture medium. A Ca2+-dependent neuronal cell degeneration was observed after prolonged and transient exposure 30 mic...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Pauwels PJ,Van Assouw HP,Leysen JE,Janssen PA

    更新日期:1989-10-01 00:00:00

  • Molecular determinants of proton-sensitive N-methyl-D-aspartate receptor gating.

    abstract::Extracellular protons inhibit N-methyl-D-aspartate (NMDA) receptors with an IC50 value in the physiological pH range. To identify the molecular determinants of proton sensitivity, we used scanning mutagenesis of the NR1 subunit to search for residues that control proton inhibition of NMDA receptors. Homology modeling ...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.63.6.1212

    authors: Low CM,Lyuboslavsky P,French A,Le P,Wyatte K,Thiel WH,Marchan EM,Igarashi K,Kashiwagi K,Gernert K,Williams K,Traynelis SF,Zheng F

    更新日期:2003-06-01 00:00:00

  • Role of thymidine kinase and thymidylate synthetase in the cytostatic, antimetabolic, and antitumor effects of the carbocyclic analogue of 5-nitro-2'-deoxyuridine. A comparison with 5-nitro-2'-deoxyuridine.

    abstract::The carbocyclic analogue of 5-nitro-2'-deoxyuridine (NO2dUrd), in which the sugar moiety is replaced by a cyclopentane ring and which was designated C-NO2dUrd, has been evaluated for its cytostatic, antimetabolic, and antitumor properties. The following findings are noted. C-NO2dUrd is about 500- to 2000-fold less inh...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:

    authors: Balzarini J,De Clercq E,Herdewijn P,Robins MJ

    更新日期:1985-05-01 00:00:00

  • Activation of trimeric P2X2 receptors by fewer than three ATP molecules.

    abstract::P2X receptors are trimeric membrane proteins. When they bind extracellular ATP, a conformational change occurs that opens a transmembrane ion channel. The ATP-binding pocket is formed in a cleft between two subunits, and a critical amino acid residue for ATP contact is Lys⁶⁹ (P2X2 numbering). In the present work, we s...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.112.080903

    authors: Stelmashenko O,Lalo U,Yang Y,Bragg L,North RA,Compan V

    更新日期:2012-10-01 00:00:00

  • A new bis-indole, KARs, induces selective M arrest with specific spindle aberration in neuroblastoma cell line SH-SY5Y.

    abstract::KARs, new semisynthetic antitumor bis-indole derivatives, were found to be inhibitors of tubulin polymerization with lower toxicity than vinblastine or vincristine, used in chemotherapy. Here, we compare the effect of KARs with those of vinblastine and vincristine on cell viability, cell proliferation, and cell cycle ...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.60.6.1235

    authors: Comín-Anduix B,Agell N,Bachs O,Ovádi J,Cascante M

    更新日期:2001-12-01 00:00:00

  • Gadolinium chloride blocks alcohol-dependent liver toxicity in rats treated chronically with intragastric alcohol despite the induction of CYP2E1.

    abstract::Hepatic CYP2E1 is induced in several models of alcohol administration, but clinically relevant pathology is only observed in rats in a model involving the continuous intragastric administration of an ethanol-containing, corn oil-based, high-fat diet. The level of CYP2E1 correlates with the degree of liver pathology in...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.51.6.944

    authors: Koop DR,Klopfenstein B,Iimuro Y,Thurman RG

    更新日期:1997-06-01 00:00:00

  • Protein RS1 (RSC1A1) Downregulates the Exocytotic Pathway of Glucose Transporter SGLT1 at Low Intracellular Glucose via Inhibition of Ornithine Decarboxylase.

    abstract::Na+-d-glucose cotransporter 1 (SGLT1) is rate-limiting for glucose absorption in the small intestine. Shortly after intake of glucose-rich food, SGLT1 abundance in the luminal membrane of the small intestine is increased. This upregulation occurs via glucose-induced acceleration of the release of SGLT1-containing vesi...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.116.104521

    authors: Chintalapati C,Keller T,Mueller TD,Gorboulev V,Schäfer N,Zilkowski I,Veyhl-Wichmann M,Geiger D,Groll J,Koepsell H

    更新日期:2016-11-01 00:00:00

  • D1-like dopaminergic activation of phosphoinositide hydrolysis is independent of D1A dopamine receptors: evidence from D1A knockout mice.

    abstract::Accumulated evidence suggests that dopamine and dopamine D1 agonists can activate phospholipase C in both brain and peripheral tissue. The receptor that mediates the hydrolysis of phosphoinositides has not been identified. The cloned dopamine D1A receptor that is generally thought to be linked to adenylyl cyclase, has...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.51.1.6

    authors: Friedman E,Jin LQ,Cai GP,Hollon TR,Drago J,Sibley DR,Wang HY

    更新日期:1997-01-01 00:00:00

  • Direct and differential interaction of beta-arrestins with the intracellular domains of different opioid receptors.

    abstract::beta-arrestins have been shown to play important roles in regulation of signaling and desensitization of opioid receptors in many in vivo studies. The current study was carried out to measure the direct interaction of beta-arrestins with two functional intracellular domains, the third intracellular loop (I3L) and the ...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章

    doi:10.1124/mol.59.4.758

    authors: Cen B,Xiong Y,Ma L,Pei G

    更新日期:2001-04-01 00:00:00

  • Modulators of CXCR4 and CXCR7/ACKR3 Function.

    abstract::The two G protein-coupled receptors (GPCRs) C-X-C chemokine receptor type 4 (CXCR4) and atypical chemokine receptor 3 (ACKR3) are part of the class A chemokine GPCR family and represent important drug targets for human immunodeficiency virus (HIV) infection, cancer, and inflammation diseases. CXCR4 is one of only thre...

    journal_title:Molecular pharmacology

    pub_type: 杂志文章,评审

    doi:10.1124/mol.119.117663

    authors: Adlere I,Caspar B,Arimont M,Dekkers S,Visser K,Stuijt J,de Graaf C,Stocks M,Kellam B,Briddon S,Wijtmans M,de Esch I,Hill S,Leurs R

    更新日期:2019-12-01 00:00:00