guanosine-triphosphate has been researched along with Disease-Resistance* in 4 studies
4 other study(ies) available for guanosine-triphosphate and Disease-Resistance
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CryoEM structure of MxB reveals a novel oligomerization interface critical for HIV restriction.
Human dynamin-like, interferon-induced myxovirus resistance 2 (Mx2 or MxB) is a potent HIV-1 inhibitor. Antiviral activity requires both the amino-terminal region of MxB and protein oligomerization, each of which has eluded structural determination due to difficulties in protein preparation. We report that maltose binding protein-fused, full-length wild-type MxB purifies as oligomers and further self-assembles into helical arrays in physiological salt. Guanosine triphosphate (GTP), but not guanosine diphosphate, binding results in array disassembly, whereas subsequent GTP hydrolysis allows its reformation. Using cryo-electron microscopy (cryoEM), we determined the MxB assembly structure at 4.6 Å resolution, representing the first near-atomic resolution structure in the mammalian dynamin superfamily. The structure revealed previously described and novel MxB assembly interfaces. Mutational analyses demonstrated a critical role for one of the novel interfaces in HIV-1 restriction. Topics: Anti-HIV Agents; Cryoelectron Microscopy; Disease Resistance; Guanosine Triphosphate; Host-Pathogen Interactions; Humans; Models, Molecular; Myxovirus Resistance Proteins; Protein Binding; Protein Conformation; Protein Multimerization; Recombinant Fusion Proteins; Structure-Activity Relationship | 2017 |
Crucial roles of TNFAIP8 protein in regulating apoptosis and Listeria infection.
TNF-α-induced protein 8 (TNFAIP8 or TIPE) is a newly described regulator of cancer and infection. However, its precise roles and mechanisms of actions are not well understood. We report in this article that TNFAIP8 regulates Listeria monocytogenes infection by controlling pathogen invasion and host cell apoptosis in a RAC1 GTPase-dependent manner. TNFAIP8-knockout mice were resistant to lethal L. monocytogenes infection and had reduced bacterial load in the liver and spleen. TNFAIP8 knockdown in murine liver HEPA1-6 cells increased apoptosis, reduced bacterial invasion into cells, and resulted in dysregulated RAC1 activation. TNFAIP8 could translocate to plasma membrane and preferentially associate with activated RAC1-GTP. The combined effect of reduced bacterial invasion and increased sensitivity to TNF-α-induced clearance likely protected the TNFAIP8-knockout mice from lethal listeriosis. Thus, by controlling bacterial invasion and the death of infected cells through RAC1, TNFAIP8 regulates the pathogenesis of L. monocytogenes infection. Topics: Animals; Apoptosis; Apoptosis Regulatory Proteins; Disease Resistance; Guanosine Triphosphate; Listeria monocytogenes; Listeriosis; Mice; Mice, Knockout; Models, Biological; Protein Binding; rac1 GTP-Binding Protein; Tumor Necrosis Factor-alpha | 2015 |
The E2-like conjugation enzyme Atg3 promotes binding of IRG and Gbp proteins to Chlamydia- and Toxoplasma-containing vacuoles and host resistance.
Cell-autonomous immunity to the bacterial pathogen Chlamydia trachomatis and the protozoan pathogen Toxoplasma gondii is controlled by two families of Interferon (IFN)-inducible GTPases: Immunity Related GTPases (IRGs) and Guanylate binding proteins (Gbps). Members of these two GTPase families associate with pathogen-containing vacuoles (PVs) and solicit antimicrobial resistance pathways specifically to the intracellular site of infection. The proper delivery of IRG and Gbp proteins to PVs requires the autophagy factor Atg5. Atg5 is part of a protein complex that facilitates the transfer of the ubiquitin-like protein Atg8 from the E2-like conjugation enzyme Atg3 to the lipid phosphatidylethanolamine. Here, we show that Atg3 expression, similar to Atg5 expression, is required for IRG and Gbp proteins to dock to PVs. We further demonstrate that expression of a dominant-active, GTP-locked IRG protein variant rescues the PV targeting defect of Atg3- and Atg5-deficient cells, suggesting a possible role for Atg proteins in the activation of IRG proteins. Lastly, we show that IFN-induced cell-autonomous resistance to C. trachomatis infections in mouse cells depends not only on Atg5 and IRG proteins, as previously demonstrated, but also requires the expression of Atg3 and Gbp proteins. These findings provide a foundation for a better understanding of IRG- and Gbp-dependent cell-autonomous resistance and its regulation by Atg proteins. Topics: Animals; Autophagy-Related Protein 5; Autophagy-Related Proteins; Chlamydia Infections; Chlamydia trachomatis; Chromosomes, Mammalian; Disease Resistance; GTP-Binding Proteins; Guanosine Triphosphate; Immunity; Inclusion Bodies; Interferon-gamma; Mice; Microtubule-Associated Proteins; Mutant Proteins; Protein Binding; Toxoplasma; Toxoplasmosis; Ubiquitin-Conjugating Enzymes; Vacuoles | 2014 |
Pathogen-driven adaptive evolution of myxovirus resistance (Mx) genes in fishes.
Myxovirus resistance (Mx) proteins, which belong to the dynamin super-family, are known to inhibit RNA viral replication in a wide range of taxonomic groups, including fishes. Given their crucial role in host immune defense, the key amino acid residues in the GTP effector domain (GED) near the C-terminus are expected to evolve adaptively in order to protect the host against invading viral pathogens. The present study reveals the role of recombination and positive selection in the evolution of Mx proteins in fishes. While the GTP-binding domain in the N-terminal domain has experienced purifying selection, several amino acid residues in GED have evolved under positive selection, thus indicating adaptive evolution. Given the antiviral activity of GED, the adaptive evolutionary changes that were observed in this region are therefore predicted to be pathogen-driven. Topics: Amino Acid Sequence; Animals; Disease Resistance; Evolution, Molecular; Fishes; Guanosine Triphosphate; Immune System; Likelihood Functions; Myxovirus Resistance Proteins; Orthomyxoviridae; Phylogeny; Protein Structure, Tertiary; Recombinant Proteins; Recombination, Genetic; Selection, Genetic | 2013 |