High affinity interaction between histidine-rich glycoprotein and the cell surface type ATP synthase on T-cells (Q24321575)

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Yoshitaka Ikemoto

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Ayako Usami

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Takehiko Koide

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Sadao Wakabayashi

Biochimica et Biophysica Acta

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language of work or name

English

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publication date

May 2009

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published in

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volume

1788

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issue

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page(s)

1099-107

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cites work

Induction of T-lymphocyte adhesion by histidine-proline-rich glycoprotein and concanavalin A

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Cell surface adenylate kinase activity regulates the F(1)-ATPase/P2Y (13)-mediated HDL endocytosis pathway on human hepatocytes.

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Histidine-rich glycoprotein is evolutionarily related to the cystatin superfamily. Presence of two cystatin domains in the N-terminal region

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Cholesterol loading increases the translocation of ATP synthase beta chain into membrane caveolae in vascular endothelial cells.

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The F(1)F(0) ATP synthase and mitochondrial respiratory chain complexes are present on the plasma membrane of an osteosarcoma cell line: An immunocytochemical study

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Amino acid sequence of human histidine-rich glycoprotein derived from the nucleotide sequence of its cDNA

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Ectopic beta-chain of ATP synthase is an apolipoprotein A-I receptor in hepatic HDL endocytosis

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Endothelial cell surface F1-F0 ATP synthase is active in ATP synthesis and is inhibited by angiostatin

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Interaction of the C-terminal domain of p43 and the alpha subunit of ATP synthase. Its functional implication in endothelial cell proliferation

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Effect of His-Gly-Lys Motif Derived from Domain 5 of High Molecular Weight Kininogen on Suppression of Cancer Metastasis Both in Vitro and in Vivo

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Histidine-rich glycoprotein binds to cell-surface heparan sulfate via its N-terminal domain following Zn2+ chelation

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Histidine-rich glycoprotein specifically binds to necrotic cells via its amino-terminal domain and facilitates necrotic cell phagocytosis

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Human keratinocytes release ATP and utilize three mechanisms for nucleotide interconversion at the cell surface

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Domain 5 of high molecular weight kininogen is antibacterial

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A novel ligand in lymphocyte-mediated cytotoxicity: expression of the beta subunit of H+ transporting ATP synthase on the surface of tumor cell lines

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Human histidine-rich glycoprotein: simultaneous purification with antithrombin III and characterization of its gross structure

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Histidine-rich glycoprotein binding to activated human platelets

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Histidine-rich glycoprotein binding to T-cell lines and its effect on T-cell substratum adhesion is strongly potentiated by zinc

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Autorosette Inhibition Factor: Isolation and Properties of the Human Plasma Protein

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Histidine-rich glycoprotein: A novel adaptor protein in plasma that modulates the immune, vascular and coagulation systems

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Enhanced blood coagulation and fibrinolysis in mice lacking histidine-rich glycoprotein (HRG)

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Chemically modified thrombin and anhydrothrombin that differentiate macromolecular substrates of thrombin

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Histidine-rich glycoprotein exerts antibacterial activity.

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Endothelial cell surface ATP synthase-triggered caspase-apoptotic pathway is essential for k1-5-induced antiangiogenesis

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A fragment of histidine-rich glycoprotein is a potent inhibitor of tumor vascularization

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Peptides derived from the histidine-proline domain of the histidine-proline-rich glycoprotein bind to tropomyosin and have antiangiogenic and antitumor activities

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Angiostatin is directly cytotoxic to tumor cells at low extracellular pH: a mechanism dependent on cell surface-associated ATP synthase

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Histidine-proline rich glycoprotein (HPRG) binds and transduces anti-angiogenic signals through cell surface tropomyosin on endothelial cells

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Intracellular signaling for vasoconstrictor coupling factor 6: novel function of beta-subunit of ATP synthase as receptor

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Histidine-rich glycoprotein binds to DNA and Fc gamma RI and potentiates the ingestion of apoptotic cells by macrophages

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