F. Boulay

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The leukocyte chemotactic receptor FPR2, but not the closely related FPR1, is sensitive to cell-penetrating pepducins with amino acid sequences descending from the third intracellular receptor loop.

Tudor I. Oprea, T. Oprea, A. Karlsson, 2013, Biochimica et biophysica acta.

Structural changes of the ligand and of the receptor alters the receptor preference for neutrophil activating peptides starting with a formylmethionyl group.

C. Dahlgren, H. Forsman, F. Boulay, 2015, Biochimica et biophysica acta.

Formylpeptide receptors in GtoPdb v.2021.2

Jilly F. Evans, S. Dahlén, M. Parmentier, 2021 .

The N-formyl peptide receptors and the anaphylatoxin C5a receptors: An overview

F. Boulay, M. Rabiet, E. Huet, 2007, Biochimie.

Broad immunocytochemical localization of the formylpeptide receptor in human organs, tissues, and cells

J. Woska, B. Bormann, R. Ye, 1998, Cell and Tissue Research.

Complement Component 5a Receptor Oligomerization and Homologous Receptor Down-regulation*

F. Boulay, M. Rabiet, E. Huet, 2008, Journal of Biological Chemistry.

The NH2-terminal region of C5aR but not that of FPR is critical for both protein transport and ligand binding.

F. Boulay, L. Méry, L. Méry, 1994, The Journal of biological chemistry.

The Synthetic Peptide Trp-Lys-Tyr-Met-Val-Met-NH2 Specifically Activates Neutrophils through FPRL1/Lipoxin A4 Receptors and Is an Agonist for the Orphan Monocyte-expressed Chemoattractant Receptor FPRL2*

C. Dahlgren, T. Christophe, F. Boulay, 2001, The Journal of Biological Chemistry.

Phagocyte Chemoattractant Receptors

M. Tardif, F. Boulay, E. Giannini, 1997, Annals of the New York Academy of Sciences.

A proinflammatory peptide from Helicobacter pylori activates monocytes to induce lymphocyte dysfunction and apoptosis.

K. Hellstrand, A. Romero, C. Dahlgren, 2001, The Journal of clinical investigation.

Expression of transcripts for two interleukin 8 receptors in human phagocytes, lymphocytes and melanoma cells.

M. Baggiolini, B. Moser, F. Boulay, 1993, The Biochemical journal.

Direct binding of a fragment of the Wiskott-Aldrich syndrome protein to the C-terminal end of the anaphylatoxin C5a receptor.

M. Tardif, F. Boulay, M. Rabiet, 2003, The Biochemical journal.

Subcellular localization and translocation of the receptor for N-formylmethionyl-leucyl-phenylalanine in human neutrophils.

L. Kjeldsen, N. Borregaard, F. Boulay, 1994, The Biochemical journal.

Serum amyloid A mediates human neutrophil production of reactive oxygen species through a receptor independent of formyl peptide receptor like‐1

A. Karlsson, C. Dahlgren, J. Bylund, 2008, Journal of leukocyte biology.

International Union of Basic and Clinical Pharmacology. LXXIII. Nomenclature for the Formyl Peptide Receptor (FPR) Family

Marc Parmentier, Charles N. Serhan, Claes Dahlgren, 2009, Pharmacological Reviews.

Binding Domain of Gelsolin 2 Selective Peptides Descending from a PIP Profile of Formyl Peptide Receptor 2 Structural Characterization and Inhibitory

H. Forsman, F. Boulay, M. Rabiet, 2012 .

Structural Characterization and Inhibitory Profile of Formyl Peptide Receptor 2 Selective Peptides Descending from a PIP2-Binding Domain of Gelsolin

C. Dahlgren, H. Forsman, F. Boulay, 2012, The Journal of Immunology.

N-Formyl Peptide Receptor 3 (FPR3) Departs from the Homologous FPR2/ALX Receptor with Regard to the Major Processes Governing Chemoattractant Receptor Regulation, Expression at the Cell Surface, and Phosphorylation

C. Dahlgren, F. Boulay, M. Rabiet, 2011, The Journal of Biological Chemistry.

The role of beta-arrestins in the formyl peptide receptor-like 1 internalization and signaling.

Sophie Barral, F. Boulay, M. Rabiet, 2007, Cellular signalling.

Phagocyte Activation by Trp–Lys–Tyr–Met–Val–Met, Acting through FPRL1/LXA4R, is not Affected by Lipoxin A4

A. Karlsson, C. Dahlgren, T. Christophe, 2002, Scandinavian journal of immunology.

Agonist-dependent phosphorylation of N-formylpeptide and activation peptide from the fifth component of C (C5a) chemoattractant receptors in differentiated HL60 cells.

M. Tardif, F. Boulay, L. Brouchon, 1993, Journal of immunology.

Tumour necrosis factor (TNF)‐α primes murine neutrophils when triggered via formyl peptide receptor‐related sequence 2, the murine orthologue of human formyl peptide receptor‐like 1, through a process involving the type I TNF receptor and subcellular granule mobilization

C. Dahlgren, H. Forsman, J. Bylund, 2008, Immunology.

Formylpeptide receptors (version 2019.4) in the IUPHAR/BPS Guide to Pharmacology Database

Marc Parmentier, Charles N. Serhan, Takao Shimizu, 2019, IUPHAR/BPS Guide to Pharmacology CITE.

The synthetic chemoattractant Trp-Lys-Tyr-Met-Val-DMet activates neutrophils preferentially through the lipoxin A(4) receptor.

A. Karlsson, C. Dahlgren, T. Christophe, 2000, Blood.

Phosphorylation of Key Serine Residues Is Required for Internalization of the Complement 5a (C5a) Anaphylatoxin Receptor via a β-Arrestin, Dynamin, and Clathrin-dependent Pathway*

L. Braun, T. Christophe, F. Boulay, 2003, The Journal of Biological Chemistry.

Human Complement 5a (C5a) Anaphylatoxin Receptor (CD88) Phosphorylation Sites and Their Specific Role in Receptor Phosphorylation and Attenuation of G Protein-mediated Responses

M. Tardif, T. Christophe, F. Boulay, 2000, The Journal of Biological Chemistry.

DIFFERENTIATED HL-60 CELLS SIGNALING PATHWAYS LEADING TO NADPH OXIDASE ACTIVATION IN RHO-GTPASE CDC42 IN THE CHEMOATTRACTANT-ELICITED INHIBITORY EFFECTS OF A DOMINANT-INTERFERING FORM OF THE

L. Braun, M. Tardif, F. Boulay, 2010 .

Posttranslational oligomerization and cooperative acid activation of mixed influenza hemagglutinin trimers

R. Webster, R. Doms, A. Helenius, 1988, The Journal of cell biology.

Selection of a C5a receptor antagonist from phage libraries attenuating the inflammatory response in immune complex disease and ischemia/reperfusion injury.

J. Köhl, A. Kola, A. Klos, 1999, Journal of immunology.

and Ischemia / Reperfusion Injury 1

J. Köhl, A. Kola, A. Klos, 1999 .

Photoaffinity labeling of mitochondrial adenosinetriphosphatase by 2-azidoadenosine 5'-[alpha-32P]diphosphate.

P. Dalbon, P. Vignais, F. Boulay, 1985, Biochemistry.

Mapping of the nucleotide-binding sites in the ADP/ATP carrier of beef heart mitochondria by photolabeling with 2-azido[alpha-32P]adenosine diphosphate.

P. Dalbon, G. Brandolin, P. Vignais, 1988, Biochemistry.

Fragmentation of the ADP/ATP carrier protein from beef heart mitochondria

G. Lauquin, P. Vignais, F. Boulay, 1979, FEBS letters.

An ADP‐ and atractyloside‐binding protein involved in ADP/ATP transport in yeast mitochondria

P. Jollès, G. Lauquin, G. Brandolin, 1979, FEBS letters.

Injection of Pseudomonas aeruginosa Exo Toxins into Host Cells Can Be Modulated by Host Factors at the Level of Translocon Assembly and/or Activity

I. Attrée, F. Boulay, M. Rabiet, 2012, PloS one.

Kinase-inactive G-protein-coupled receptor kinases are able to attenuate follicle-stimulating hormone-induced signaling.

P. Crépieux, E. Reiter, S. Marion, 2001, Biochemical and biophysical research communications.

Phosphorylation, dephosphorylation, and recycling of the C5a receptor in differentiated HL60 cells.

F. Boulay, E. Giannini, 1995, Journal of immunology.

Internalization and recycling of the C5a anaphylatoxin receptor: evidence that the agonist-mediated internalization is modulated by phosphorylation of the C-terminal domain.

F. Boulay, E. Giannini, N. Naik, 1997, Journal of cell science.

Identification of amino acid residues photolabeled with 2-azido[alpha-32P]adenosine diphosphate in the beta subunit of beef heart mitochondrial F1-ATPase.

J. Garin, J. Issartel, J. Lunardi, 1986, Biochemistry.

Evidence that the extracellular N‐terminal domain of C5aR contains amino‐acid residues crucial for C5a binding

F. Boulay, L. Méry, François Boulay, 1993, European journal of haematology.

Overexpression of wild-type and catalytically inactive forms of GRK2 and GRK6 fails to alter the agonist-induced phosphorylation of the C5a receptor (CD88): evidence that GRK6 is autophosphorylated in COS-7 cells.

M. Tardif, T. Christophe, F. Boulay, 1999, Biochemical and biophysical research communications.

Photolabeling approach to the study of the topography of the atractyloside binding site in mitochondrial adenosine 5'-diphosphate/adenosine 5'-triphosphate carrier protein.

A. Tsugita, G. Lauquin, P. Vignais, 1983, Biochemistry.

Formyl peptide receptor-mediated proinflammatory consequences of peptide deformylase inhibition in Staphylococcus aureus.

A. Peschel, D. Mader, F. Boulay, 2010, Microbes and infection.

THE CONCISE GUIDE TO PHARMACOLOGY 2021/22: G protein‐coupled receptors

Stephen P. H. Alexander, Leigh A. Stoddart, Kalyan C. Tirupula, 2021, British journal of pharmacology.

Recent Developments in the Study of the Conformational States and the Nucleotide Binding Sites of the ADP/ATP Carrier

P. Dalbon, G. Brandolin, P. Vignais, 1989 .

Synthesis and use of a novel N-formyl peptide derivative to isolate a human N-formyl peptide receptor cDNA.

M. Tardif, P. Vignais, F. Boulay, 1990, Biochemical and biophysical research communications.

Human formyl peptide receptor 2 senses highly pathogenic Staphylococcus aureus.

T. Schöneberg, A. Peschel, M. Otto, 2010, Cell host & microbe.

Orientation of the N-terminal region of the membrane-bound ADP/ATP carrier protein explored by antipeptide antibodies and an arginine-specific endoprotease. Evidence that the accessibility of the N-terminal residues depends on the conformational state of the carrier.

P. Dalbon, G. Brandolin, P. Vignais, 1989, Biochemistry.

Immunological and Enzymatic Approaches of the Orientation of the Membrane Bound ADP/ATP Carrier

P. Dalbon, G. Brandolin, P. Vignais, 1989 .

Exploration of nucleotide binding sites in the mitochondrial membrane by 2‐azido‐[α‐32P]ADP

P. Dalbon, P. Vignais, F. Boulay, 1985 .

Localization of the N-ethylmaleimide reactive cysteine in the beef heart mitochondrial ADP/ATP carrier protein.

P. Vignais, F. Boulay, 1984, Biochemistry.

Structure and function of leukocyte chemoattractant receptors.

R. Ye, F. Boulay, Richard D. Ye, 1997, Advances in pharmacology.

Site-Directed Mutagenesis of Conserved Charged Residues in the Helical Region of the Human C5a Receptor

J. Köhl, A. Klos, W. Bautsch, 1996 .

The human N-formylpeptide receptor. Characterization of two cDNA isolates and evidence for a new subfamily of G-protein-coupled receptors.

M. Tardif, P. Vignais, F. Boulay, 1990, Biochemistry.

The Chemoattractant Receptors FPR and C5aR: Same Functions – Different Fates

F. Boulay, M. Rabiet, 2005, Traffic.

Antibacterial Activity of Pepducins, Allosterical Modulators of Formyl Peptide Receptor Signaling

Tudor I. Oprea, T. Oprea, C. Dahlgren, 2014, Antimicrobial Agents and Chemotherapy.

Localization of immunoreactive regions in the beef heart adenine nucleotide carrier using rabbit antisera against the carboxyatractyloside-liganded and the sodium dodecyl sulfate denaturated carrier forms.

G. Lauquin, P. Vignais, F. Boulay, 1986, Biochemistry.

Functional and Topological Aspects of the Mitochondrial Adenine Nucleotide Carrier

G. Lauquin, G. Brandolin, P. Vignais, 1982 .

Chemical modifications and active site labeling of the mitochondrial ADP/ATP carrier.

G. Lauquin, G. Brandolin, P. Vignais, 1986, Methods in enzymology.

Use of Fluorescent Probes of the Adenine Nucleotide Carrier for Binding Studies and Analysis of Conformational Changes

G. Brandolin, P. Vignais, M. Block, 1986 .

Fluorescent probes of the mitochondrial ADP/ATP carrier protein.

G. Lauquin, G. Brandolin, P. Vignais, 1986, Methods in enzymology.

6'-O-dansyl-gamma-aminobutyryl atractyloside, a fluorescent probe of the ADP/ATP carrier: exploration of conformational changes of the membrane-bound ADP/ATP carrier elicited by substrates and inhibitors.

G. Brandolin, P. Vignais, F. Boulay, 1986, Biochemical and biophysical research communications.

Human mitochondria‐derived N‐formylated peptides are novel agonists equally active on FPR and FPRL1, while Listeria monocytogenes‐derived peptides preferentially activate FPR

F. Boulay, M. Rabiet, E. Huet, 2005, European journal of immunology.

oxidase activation in differentiated HL-60 cells in the chemoattractant-elicited signaling pathways leading to NADPH Inhibitory effects of a dominant-interfering form of the Rho-GTPase Cdc42

L. Braun, M. Tardif, F. Boulay, 2010 .

Inhibitory effects of a dominant-interfering form of the Rho-GTPase Cdc42 in the chemoattractant-elicited signaling pathways leading to NADPH oxidase activation in differentiated HL-60 cells.

L. Braun, M. Tardif, F. Boulay, 2002, Blood.

Isolation and characterization of a variant HL60 cell line defective in the activation of the NADPH oxidase by phorbol myristate acetate.

M. Tardif, T. Christophe, F. Boulay, 1998, Journal of immunology.

Acetate the NADPH Oxidase by Phorbol Myristate HL 60 Cell Line Defective in the Activation of Isolation and Characterization of a Variant

M. Tardif, T. Christophe, F. Boulay, 1998 .

Membrane and Chaperone Recognition by the Major Translocator Protein PopB of the Type III Secretion System of Pseudomonas aeruginosa*

J. Simorre, A. Förster, A. Dessen, 2013, The Journal of Biological Chemistry.

Neutrophil NADPH‐oxidase activation by an annexin AI peptide is transduced by the formyl peptide receptor (FPR), whereas an inhibitory signal is generated independently of the FPR family receptors

C. Movitz, K. Hellstrand, C. Dahlgren, 2005, Journal of leukocyte biology.

A Monocyte-Specific Peptide from Herpes Simplex Virus Type 2 Glycoprotein G Activates the NADPH-Oxidase but Not Chemotaxis through a G-Protein-Coupled Receptor Distinct from the Members of the Formyl Peptide Receptor Family1

A. Karlsson, C. Dahlgren, K. Eriksson, 2007, The Journal of Immunology.

Formyl Peptide Receptor Family Receptor Distinct from the Members of the Chemotaxis through a G-Protein-Coupled Activates the NADPH-Oxidase but Not Simplex Virus Type 2 Glycoprotein G A Monocyte-Specific Peptide from Herpes

C. Dahlgren, K. Eriksson, L. Bellner, 2007 .

Proinflammatory Activity of a Cecropin-Like Antibacterial Peptide from Helicobacter pylori

Anna Karlsson, Claes Dahlgren, T. Nyström, 2001, Antimicrobial Agents and Chemotherapy.

Identification in milk of a serum amyloid A peptide chemoattractant for B lymphoblasts

D. Mollé, M. Berri, G. Henry, 2009, BMC Immunology.

Expression cloning of a receptor for C5a anaphylatoxin on differentiated HL-60 cells.

M. Tardif, P. Vignais, F. Boulay, 1991, Biochemistry.

Lipopolysaccharide-Induced Granule Mobilization and Priming of the Neutrophil Response to Helicobacter pylori Peptide Hp(2-20), Which Activates Formyl Peptide Receptor-Like 1

A. Karlsson, C. Dahlgren, J. Bylund, 2002, Infection and Immunity.

Modulation of human neutrophil function by fibronectin degradation products isolated from cryoglobulins

D. Anthony, J. Renversez, F. Morel, 1992, Inflammation.

Direct or C5a-induced Activation of Heterotrimeric Gi2 Proteins in Human Neutrophils Is Associated with Interaction between Formyl Peptide Receptors and the Cytoskeleton*

G. Bokoch, T. Andersson, F. Boulay, 1996, The Journal of Biological Chemistry.

The influenza hemagglutinin precursor as an acid‐sensitive probe of the biosynthetic pathway.

I. Wilson, R. Doms, A. Helenius, 1987, The EMBO journal.

Antibacterial Activity of Pepducins, Allosterical Modulators of

Tudor I. Oprea, C. Dahlgren, H. Forsman, 2014 .

Receptor Signaling Allosterical Modulators of Formyl Peptide Antibacterial Activity of Pepducins

Tudor I. Oprea, C. Dahlgren, H. Forsman, 2014 .

Site-directed mutagenesis of conserved charged residues in the helical region of the human C5a receptor. Arg2O6 determines high-affinity binding sites of C5a receptor.

J. Köhl, A. Klos, W. Bautsch, 1996, European journal of biochemistry.

oxidase activation in differentiated HL-60 cells in the chemoattractant-elicited signaling pathways leading to NADPH Inhibitory effects of a dominant-interfering form of the Rho-GTPase Cdc42

L. Braun, M. Tardif, F. Boulay, 2010 .

The peptide Trp-Lys-Tyr-Met-Val-D-Met activates neutrophils through the formyl peptide receptor only when signaling through the formylpeptide receptor like 1 is blocked. A receptor switch with implications for signal transduction studies with inhibitors and receptor antagonists.

C. Dahlgren, J. Bylund, F. Boulay, 2006, Biochemical pharmacology.