journal
https://read.qxmd.com/read/38604564/hypothiocyanous-acid-reductase-is-critical-for-host-colonization-and-infection-by-streptococcus-pneumoniae
#21
JOURNAL ARTICLE
Heather L Shearer, Michael J Currie, Hannah N Agnew, Claudia Trappetti, Frederick Stull, Paul E Pace, James C Paton, Renwick C J Dobson, Nina Dickerhof
The major human pathogen Streptococcus pneumoniae encounters the immune-derived oxidant hypothiocyanous acid (HOSCN) at sites of colonization and infection. We recently identified the pneumococcal hypothiocyanous acid reductase (Har), a member of the flavoprotein disulfide reductase enzyme family, and showed that it contributes to the HOSCN tolerance of S. pneumoniae in vitro. Here, we demonstrate in mouse models of pneumococcal infection that Har is critical for colonization and invasion. In a colonization model, bacterial load was attenuated dramatically in the nasopharynx when har was deleted in S...
April 9, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38599381/tfe3-slc36a1-axis-promotes-resistance-to-glucose-starvation-in-kidney-cancer-cells
#22
JOURNAL ARTICLE
Suli Lv, Zongbiao Zhang, Zhenyong Li, Qian Ke, Xianyun Ma, Neng Li, Xuefeng Zhao, Qingli Zou, Lidong Sun, Tanjing Song
Higher demand for nutrients including glucose is characteristic of cancer. "Starving cancer" has been pursued to curb tumor progression. An ,intriguing regime is to inhibit glucose transporter GLUT1 in cancer cells. In addition, during cancer progression, cancer cells may suffer from insufficient glucose supply. Yet cancer cells can somehow tolerate glucose starvation. Uncovering the underlying mechanisms shall not only shed insight into cancer progression but also benefit cancer therapy. TFE3 is a transcription factor known to activate autophagic genes...
April 8, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38599380/a-novel-system-to-determine-activity-of-individual-uridine-5-diphospho-glucuronosyltransferase-ugt-isoforms-recombinant-ugt-beads
#23
JOURNAL ARTICLE
Ting Wang, Mitchell E Taub, Tom S Chan
Previous work demonstrated that human liver microsomes (HLM) can spontaneously bind to silica-coated magnetizable beads (HLM-beads) and that these HLM-beads retain UGT activity. However, the contributions of individual UGT isoforms is not directly assessable in this system except through use of model inhibitors. Thus, a preparation wherein rUGT microsomes bound to these same beads to form rUGT-beads of individual UGT isoforms would provide a novel system for measuring the contribution of individual UGT isoforms in a direct manner...
April 8, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38588814/biochemical-characterization-of-e-coli-dnac-variants-that-alter-dnab-helicase-loading-onto-dna
#24
JOURNAL ARTICLE
Sarah D McMillan, James L Keck
DNA replication in E. coli starts with loading of the replicative helicase, DnaB, onto DNA. This reaction requires the DnaC loader protein, which forms a 6:6 complex with DnaB and opens a channel in the DnaB hexamer through which single-stranded DNA is thought to pass. During replication, replisomes frequently encounter DNA damage and nucleoprotein complexes that can lead to replication fork collapse. Such events require DnaB re-loading onto DNA to allow replication to continue. Replication restart proteins mediate this process by recruiting DnaB6 /DnaC6 to abandoned DNA replication forks...
April 6, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38588813/impaired-malin-expression-and-interaction-with-partner-proteins-in-lafora-disease
#25
JOURNAL ARTICLE
Alexander V Skurat, Dyann M Segvich, Christopher J Contreras, Yueh-Chiang Hu, Thomas D Hurley, Anna A DePaoli-Roach, Peter J Roach
Lafora disease (LD) is an autosomal recessive myoclonus epilepsy with onset in the teenage years leading to death within a decade of onset. LD is characterized by the overaccumulation of hyperphosphorylated, poorly branched, insoluble, glycogen-like polymers called Lafora bodies. The disease is caused by mutations in either EPM2A, encoding laforin, a dual specificity phosphatase that dephosphorylates glycogen, or EMP2B, encoding malin, an E3-ubiquitin ligase. While glycogen is a widely accepted laforin substrate, substrates for malin have been difficult to identify partly due to the lack of malin antibodies able to detect malin in vivo...
April 6, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38588812/immunometabolic-crosstalk-in-aedes-fluviatilis-wolbachia-pipientis-symbiosis
#26
JOURNAL ARTICLE
Jhenifer Nascimento da Silva, Christiano Calixto Conceição, Gisely Cristina Ramos de Brito, Carlos Renato de Oliveira Daumas Filho, Ana Beatriz Walter Nuno, Octavio A C Talyuli, Angélica Arcanjo, Pedro L de Oliveira, Luciano Andrade Moreira, Itabajara da Silva Vaz, Carlos Logullo
Wolbachia pipientis is a maternally transmitted symbiotic bacterium that mainly colonizes arthropods, potentially affecting different aspects of the host's physiology, e.g. reproduction, immunity, and metabolism. It has been shown that Wolbachia modulates glycogen metabolism in mosquito Aedes fluviatilis (Ae. fluviatilis). Glycogen synthesis is controlled by the enzyme GSK3, which is also involved in immune responses in both vertebrate and invertebrate organisms. Here we investigated the mechanisms behind immune changes mediated by GSK3β in the symbiosis between Ae...
April 6, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38588811/coenzyme-q-4-is-a-functional-substitute-for-coenzyme-q-10-and-can-be-targeted-to-the-mitochondria
#27
JOURNAL ARTICLE
Laura H Steenberge, Sean Rogers, Andrew Y Sung, Jing Fan, David J Pagliarini
Coenzyme Q10 (CoQ10) is an important cofactor and antioxidant for numerous cellular processes, and its deficiency has been linked to human disorders including mitochondrial disease, heart failure, Parkinson's disease, and hypertension. Unfortunately, treatment with exogenous CoQ10 is often ineffective, likely due to the extreme hydrophobicity and high molecular weight of CoQ10 . Here, we show that less hydrophobic CoQ species with shorter isoprenoid tails can serve as viable substitutes for CoQ10 in human cells...
April 6, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38588810/ancestral-sequence-reconstruction-dissects-structural-and-functional-differences-among-eosinophil-ribonucleases
#28
JOURNAL ARTICLE
Thi Thanh Quynh Tran, Chitra Narayanan, Andrea N Loes, Timothy H Click, N T Hang Pham, Myriam Létourneau, Michael J Harms, Charles Calmettes, Pratul K Agarwal, Nicolas Doucet
Evolutionarily conserved structural folds can give rise to diverse biological functions, yet predicting atomic-scale interactions that contribute to the emergence of novel activities within such folds remains challenging. Pancreatic-type ribonucleases illustrate this complexity, sharing a core structure that has evolved to accommodate varied functions. In this study, we used ancestral sequence reconstruction to probe evolutionary and molecular determinants that distinguish biological activities within eosinophil members of the RNase 2/3 subfamily...
April 6, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38588809/ykt6-functionally-overlaps-with-vacuolar-and-exocytic-r-snares-in-the-yeast-saccharomyces-cerevisiae
#29
JOURNAL ARTICLE
Hayate Watanabe, Shingo Urano, Nozomi Kikuchi, Yurika Kubo, Ayumi Kikuchi, Katsuya Gomi, Takahiro Shintani
The soluble N-ethylmaleimide-sensitive factor attachment protein receptor (SNARE) complex forms a 4-helix coiled-coil bundle consisting of 16 layers of interacting side chains upon membrane fusion. The central layer (layer 0) is highly conserved and comprises three glutamines (Q) and one arginine (R), and thus SNAREs are classified into Qa-, Qb-, Qc-, and R-SNAREs. Homotypic vacuolar fusion in Saccharomyces cerevisiae requires the SNAREs Vam3 (Qa), Vti1 (Qb), Vam7 (Qc), and Nyv1 (R). However, the yeast strain lacking NYV1 (nyv1Δ) shows no vacuole fragmentation, whereas the vam3Δ and vam7Δ strains display fragmented vacuoles...
April 6, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38588808/mitotic-spindle-positioning-protein-misp-preferentially-binds-to-aged-f-actin
#30
JOURNAL ARTICLE
E Angelo Morales, Gillian N Fitz, Matthew J Tyska
Actin bundling proteins crosslink filaments into polarized structures that shape and support membrane protrusions including filopodia, microvilli, and stereocilia. In the case of epithelial microvilli, mitotic spindle positioning protein (MISP) is an actin bundler that localizes specifically to the basal rootlets, where the pointed ends of core bundle filaments converge. Previous studies established that MISP is prevented from binding more distal segments of the core bundle by competition with other actin binding proteins...
April 6, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38588807/functional-identification-of-bacterial-spermine-thermospermine-norspermine-norspermidine-spermidine-and-n-1-aminopropylagmatine-synthases
#31
JOURNAL ARTICLE
Bin Li, Jue Liang, Hamid R Baniasadi, Shin Kurihara, Margaret A Phillips, Anthony J Michael
Spermine synthase is an aminopropyltransferase that adds an aminopropyl group to the essential polyamine spermidine to form tetraamine spermine, needed for normal human neural development, plant salt and drought resistance, and yeast CoA biosynthesis. We functionally identify for the first time bacterial spermine synthases, derived from phyla Bacillota, Rhodothermota, Thermodesulfobacteriota, Nitrospirota, Deinococcota and Pseudomonadota. We also identify bacterial aminopropyltransferases that synthesize the spermine same mass isomer thermospermine, from phyla Cyanobacteriota, Thermodesulfobacteriota, Nitrospirota, Dictyoglomota, Armatimonadota and Pseudomonadota, including the human opportunistic pathogen Pseudomonas aeruginosa...
April 6, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38588806/arv1-deficiency-induces-lipid-bilayer-stress-and-enhances-rdna-stability-by-activating-the-unfolded-protein-response-in-saccharomyces-cerevisiae
#32
JOURNAL ARTICLE
Sujin Hong, Hyeon-Geun Lee, Won-Ki Huh
The stability of ribosomal DNA (rDNA) is maintained through transcriptional silencing by the NAD+ -dependent histone deacetylase Sir2 in Saccharomyces cerevisiae. Alongside proteostasis, rDNA stability is a crucial factor regulating the replicative lifespan (RLS) of S. cerevisiae. The unfolded protein response (UPR) is induced by misfolding of proteins or an imbalance of membrane lipid composition and is responsible for degrading misfolded proteins and restoring endoplasmic reticulum (ER) membrane homeostasis...
April 6, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38588805/spatial-organization-of-bacterial-sphingolipid-synthesis-enzymes
#33
JOURNAL ARTICLE
Chioma G Uchendu, Ziqiang Guan, Eric A Klein
Sphingolipids are produced by nearly all eukaryotes where they play significant roles in cellular processes such as cell growth, division, programmed cell death, angiogenesis, and inflammation. While it was previously believed that sphingolipids were quite rare among bacteria, bioinformatic analysis of the recently identified bacterial sphingolipid synthesis genes suggests that these lipids are likely to be produced by a wide range of microbial species. The sphingolipid synthesis pathway consists of three critical enzymes...
April 6, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38588804/the-luciferase-based-in-vivo-protein-protein-interaction-assay-revealed-that-chk1-promotes-pp2a-and-pme-1-interaction
#34
JOURNAL ARTICLE
Sana Ando, Keiko Tanaka, Maharu Matsumoto, Yuki Oyama, Yuri Tomabechi, Atsushi Yamagata, Mikako Shirouzu, Reiko Nakagawa, Noriaki Okimoto, Makoto Taiji, Koichi Sato, Takashi Ohama
Protein phosphatase 2A (PP2A) is an essential serine/threonine protein phosphatase, and its dysfunction is involved in the onset of cancer and neurodegenerative disorders. PP2A functions as a trimeric holoenzyme whose composition is regulated by the methyl-esterification (methylation) of the PP2A catalytic subunit (PP2Ac). Protein phosphatase methylesterase-1 (PME-1) is the sole PP2Ac methylesterase, and the higher PME-1 expression is observed in various cancer and neurodegenerative diseases. Apart from serving as a methylesterase, PME-1 acts as a PP2A inhibitory protein, binding directly to PP2Ac and suppressing its activity...
April 6, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38583864/pathogenic-residue-insertion-in-a-neuronal-nicotinic-receptor-alters-intra-and-inter-subunit-interactions-that-tune-channel-gating
#35
JOURNAL ARTICLE
Deborah J Msekela, Steven M Sine
We describe molecular-level functional changes in the α4β2 nicotinic acetylcholine receptor (nAChR) by a leucine residue insertion in the M2 transmembrane domain of the α4 subunit associated with sleep-related hyperkinetic epilepsy. Measurements of agonist-elicited single channel currents reveal the primary effect is to stabilize the open channel state while the secondary effect is to promote reopening of the channel. These dual effects prolong the durations of bursts of channel openings equally for the two major stoichiometric forms of the receptor, (α4)2 (β2)3 and (α4)3 (β2)2 , indicating the functional impact is independent of mutant copy number per receptor...
April 5, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38583863/phospholamban-inhibits-the-cardiac-calcium-pump-by-interrupting-an-allosteric-activation-pathway
#36
JOURNAL ARTICLE
Sean R Cleary, Jaroslava Seflova, Ellen E Cho, Konark Bisht, Himanshu Khandelia, L Michel Espinoza-Fonseca, Seth L Robia
Phospholamban (PLB) is a transmembrane micropeptide that regulates the Ca2+ pump SERCA in cardiac muscle, but the physical mechanism of this regulation remains poorly understood. PLB reduces the Ca2+ sensitivity of active SERCA, increasing the Ca2+ concentration required for pump cycling. However, PLB does not decrease Ca2+ binding to SERCA when ATP is absent, suggesting PLB does not inhibit SERCA Ca2+ affinity. The prevailing explanation for these seemingly conflicting results is that PLB slows transitions in the SERCA enzymatic cycle associated with Ca2+ binding, altering transport Ca2+ dependence without actually affecting the equilibrium binding affinity of the Ca2+ -coordinating sites...
April 5, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38582453/selenoprotein-i-is-indispensable-for-ether-lipid-homeostasis-and-proper-myelination
#37
JOURNAL ARTICLE
Lance G A Nunes, Chi Ma, FuKun W Hoffmann, Ashley E Shay, Matthew W Pitts, Peter R Hoffmann
Selenoprotein I (SELENOI) catalyzes the final reaction of the CDP-ethanolamine branch of the Kennedy pathway, generating the phospholipids phosphatidylethanolamine (PE) and plasmenyl-PE. Plasmenyl-PE is a key component of myelin and is characterized by a vinyl ether bond that preferentially reacts with oxidants, thus serves as a sacrificial antioxidant. In humans, multiple loss-of-function mutations in genes affecting plasmenyl-PE metabolism have been implicated in hereditary spastic paraplegia (HSP), including SELENOI...
April 4, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38582452/the-sensor-of-the-bacterial-histidine-kinase-cpxa-is-a-novel-dimer-of-extracytoplasmic-per-arnt-sim-pas-domains
#38
JOURNAL ARTICLE
Timothy H S Cho, Cameron Murray, Roxana Malpica, Rodrigo Margain-Quevedo, Gina L Thede, Jun Lu, Ross A Edwards, J N Mark Glover, Tracy L Raivio
Histidine kinases are key bacterial sensors that recognize diverse environmental stimuli. While mechanisms of phosphorylation and phosphotransfer by cytoplasmic kinase domains are relatively well-characterized, the ways in which extracytoplasmic sensor domains regulate activation remain mysterious. The Cpx envelope stress response is a conserved Gram-negative two-component system which is controlled by the sensor kinase CpxA. We report the structure of the Escherichia coli CpxA sensor domain (CpxA-SD) as a globular Per-ARNT-Sim (PAS)-like fold highly similar to that of Vibrio parahaemolyticus CpxA as determined by X-ray crystallography...
April 4, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38582451/jnk-activity-modulates-postsynaptic-scaffold-protein-sap102-and-kainate-receptor-dynamics-in-dendritic-spines
#39
JOURNAL ARTICLE
Stella-Amrei Kunde, Bettina Schmerl, Judith von Sivers, Elham Ahmadyar, Taanisha Gupta, Nils Rademacher, Hanna L Zieger, Sarah A Shoichet
Synapse formation depends on the coordinated expression and regulation of scaffold proteins. The JNK family kinases play a role in scaffold protein regulation, but the nature of this functional interaction in dendritic spines requires further investigation. Here, using a combination of biochemical methods and live-cell imaging strategies, we show that the dynamics of the synaptic scaffold molecule SAP102 are negatively regulated by JNK inhibition, that SAP102 is a direct phosphorylation target of JNK3, and that SAP102 regulation by JNK is restricted to neurons that harbour mature synapses...
April 4, 2024: Journal of Biological Chemistry
https://read.qxmd.com/read/38582450/the-molecular-principles-underlying-diverse-functions-of-the-slc26-family-of-proteins
#40
JOURNAL ARTICLE
Satoe Takahashi, Kazuaki Homma
Mammalian SLC26 proteins are membrane-based anion transporters that belong to the large SLC26/SulP family, and many of their variants are associated with hereditary diseases. Recent structural studies revealed a strikingly similar homodimeric molecular architecture for several SLC26 members, implying a shared molecular principle. Now a new question emerges as to how these structurally similar proteins execute diverse physiological functions. In this study we sought to identify the common vs. distinct molecular mechanism among the SLC26 proteins using both naturally occurring and artificial missense changes introduced to SLC26A4, SLC26A5, and SLC26A9...
April 4, 2024: Journal of Biological Chemistry
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