Human mitochondria-derived N-formylated peptides are novel agonists equally active on FPR and FPRL1, while Listeria monocytogenes-derived peptides preferentially activate FPR (Q28262329)

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

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

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Listeria monocytogenes

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author name string

Marie-Josèphe Rabiet

1

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Emilie Huet

2

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François Boulay

3

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language of work or name

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publication date

August 2005

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European Journal of Immunology

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35

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8

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2486-95

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The molecular biology of leukocyte chemoattractant receptors

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7 January 2021

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

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Structure and function of leukocyte chemoattractant receptors

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NADPH oxidase and the respiratory burst

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Receptor binding kinetics and cellular responses of six N-formyl peptide agonists in human neutrophils

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Further studies on the structural requirements for synthetic peptide chemoattractants

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A high potency nonformylated peptide agonist for the phagocyte N-formylpeptide chemotactic receptor

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Isolation of a cDNA that encodes a novel granulocyte N-formyl peptide receptor

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Identification of a human cDNA encoding a functional high affinity lipoxin A4 receptor

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Formyl-peptide receptors revisited

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Humanin, a newly identified neuroprotective factor, uses the G protein-coupled formylpeptide receptor-like-1 as a functional receptor

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Differential expression of members of the N-formylpeptide receptor gene cluster in human phagocytes

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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

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

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Identification and characterization of an endogenous chemotactic ligand specific for FPRL2

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Impaired antibacterial host defense in mice lacking the N-formylpeptide receptor

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Mitochondrial N-formylmethionyl proteins as chemoattractants for neutrophils

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Peptides from the amino-terminus of mouse mitochondrially encoded NADH dehydrogenase subunit 1 are potent chemoattractants

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Activation of lipoxin A(4) receptors by aspirin-triggered lipoxins and select peptides evokes ligand-specific responses in inflammation

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Specialized functions of MHC class I molecules. I. An N-formyl peptide receptor is required for construction of the class I antigen Mta.

1 reference

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7 January 2021

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H-2M3 presents a Listeria monocytogenes peptide to cytotoxic T lymphocytes

1 reference

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7 January 2021

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H2-M3, a full-service class Ib histocompatibility antigen

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7 January 2021

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Identification of an H2-M3-restricted Listeria epitope: implications for antigen presentation by M3.

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7 January 2021

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A Listeria monocytogenes pentapeptide is presented to cytolytic T lymphocytes by the H2-M3 MHC class Ib molecule.

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7 January 2021

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H2-M3 restricted presentation of a Listeria-derived leader peptide

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7 January 2021

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Nonclassical binding of formylated peptide in crystal structure of the MHC class lb molecule H2-M3

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7 January 2021

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Specialized functions of major histocompatibility complex class I molecules. II. Hmt binds N-formylated peptides of mitochondrial and prokaryotic origin

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7 January 2021

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N-Formylated humanin activates both formyl peptide receptor-like 1 and 2

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7 January 2021

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Identifiers

10.1002/EJI.200526338

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Consolidated OpenCitations Corpus – April 2017

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https://api.fatcat.wiki/v0/release/wjwtgb7zlffenmumjkyxxmjzqq

24 November 2022

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mapped directly with Wikidata item

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

PubMed publication ID

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Consolidated OpenCitations Corpus – April 2017

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