keyword
https://read.qxmd.com/read/38617285/proteasome-hyperactivation-rewires-the-proteome-enhancing-stress-resistance-proteostasis-lipid-metabolism-and-erad-in-c-elegans
#21
David Salcedo-Tacuma, Nadeeem Asad, Giovanni Howells, Raymond Anderson, David M Smith
Proteasome dysfunction is implicated in the pathogenesis of neurodegenerative diseases and age-related proteinopathies. Using a C. elegans model, we demonstrate that 20S proteasome hyperactivation, facilitated by 20S gate-opening, accelerates the targeting of intrinsically disordered proteins. This leads to increased protein synthesis, extensive rewiring of the proteome and transcriptome, enhanced oxidative stress defense, accelerated lipid metabolism, and peroxisome proliferation. It also promotes ER-associated degradation (ERAD) of aggregation-prone proteins, such as alpha-1 antitrypsin (ATZ) and various lipoproteins...
April 6, 2024: bioRxiv
https://read.qxmd.com/read/38617242/-sinorhizobium-meliloti-br-bodies-promote-fitness-during-host-colonization
#22
Kaveendya S Mallikaarachchi, Jason L Huang, Shanmukha Madras, Rodrigo A Cuellar, Zhenzhong Huang, Alisa Gega, Imalka W Rathnayaka-Mudiyanselage, Nadra Al-Husini, Natalie Saldaña-Rivera, Loi H Ma, Eric Ng, Joseph C Chen, Jared M Schrader
UNLABELLED: Biomolecular condensates, such as the nucleoli or P-bodies, are non-membrane-bound assemblies of proteins and nucleic acids that facilitate specific cellular processes. Like eukaryotic P-bodies, the recently discovered bacterial ribonucleoprotein bodies (BR-bodies) organize the mRNA decay machinery, yet the similarities in molecular and cellular functions across species have been poorly explored. Here, we examine the functions of BR-bodies in the nitrogen-fixing endosymbiont Sinorhizobium meliloti , which colonizes the roots of compatible legume plants...
April 6, 2024: bioRxiv
https://read.qxmd.com/read/38615193/map-conformational-landscapes-of-intrinsically-disordered-proteins-with-polymer-physics-quantities
#23
JOURNAL ARTICLE
Hossain Shadman, Jesse D Ziebarth, Caleb E Gallops, Ray Luo, Zhengxin Li, Hai-Feng Chen, Yongmei Wang
Disordered proteins are conformationally flexible proteins that are biologically important and have been implicated in devastating diseases such as Alzheimer's and cancer. Unlike stably-folded structured proteins, disordered proteins sample a range of different conformations that needs to be accounted for. Here, we treat disordered proteins as polymer chains, and compute a dimensionless quantity called instantaneous shape ratio (Rs ), as Rs = Ree 2 /Rg 2 , where Ree is end-to-end distance and Rg is radius of gyration...
April 12, 2024: Biophysical Journal
https://read.qxmd.com/read/38614173/impact-of-c-terminal-domains-of-paralogous-single-stranded-dna-binding-proteins-from-streptomyces-coelicolor-on-their-biophysical-properties-and-biological-functions
#24
JOURNAL ARTICLE
Goran Pipalović, Želimira Filić, Mirsada Ćehić, Tina Paradžik, Ksenija Zahradka, Ivo Crnolatac, Dušica Vujaklija
Single-stranded DNA-binding proteins (SSB) are crucial in DNA metabolism. While Escherichia coli SSB is extensively studied, the significance of its C-terminal domain has only recently emerged. This study explored the significance of C-domains of two paralogous Ssb proteins in S. coelicolor. Mutational analyses of C-domains uncovered a novel role of SsbA during sporulation-specific cell division and demonstrated that the C-tip is non-essential for survival. In vitro methods revealed altered biophysical and biochemical properties of Ssb proteins with modified C-domains...
April 11, 2024: International Journal of Biological Macromolecules
https://read.qxmd.com/read/38609329/am404-analogs-as-activators-of-the-20s-isoform-of-the-human-proteasome
#25
JOURNAL ARTICLE
Andres Salazar, Kate Kragness, Diogo Feleciano, Darci Jones Trader
The proteasome is a multisubunit protease system responsible for the majority of the protein turnover in eukaryotic organisms. Dysregulation of this enzymatic complex leads to protein accumulation, subsequent aggregation, and ultimately diseased states; for that reason, positive modulation of its activity has been recently investigated as a therapeutic strategy for neurodegenerative and age-related diseases. The small molecule AM404 was recently identified as an activator of the 20S isoform of the proteasome and further exploration of the scaffold revealed the importance of the polyunsaturated fatty acid chain to elicit activity...
April 12, 2024: Chembiochem: a European Journal of Chemical Biology
https://read.qxmd.com/read/38608858/membraneless-and-membrane-bound-organelles-in-an-anhydrobiotic-cell-line-are-protected-from-desiccation-induced-damage
#26
JOURNAL ARTICLE
Clinton J Belott, Oleg A Gusev, Takahiro Kikawada, Michael A Menze
Anhydrobiotic species can survive virtually complete water loss by entering a reversible ametabolic glassy state that may persist for years in ambient conditions. The Pv11 cell line was derived from egg mass of the anhydrobiotic midge, Polypedilum vanderplanki, and is currently the only available anhydrobiotic cell line. Our results demonstrate that the necessary preconditioning for Pv11 cells to enter anhydrobiosis causes autophagy and reduces mitochondrial respiration by over 70%. We speculate that reorganizing cellular bioenergetics to create and conserve energy stores may be valuable to successfully recover after rehydration...
April 10, 2024: Cell Stress & Chaperones
https://read.qxmd.com/read/38607226/how-hydrophobicity-side-chains-and-salt-affect-the-dimensions-of-disordered-proteins
#27
JOURNAL ARTICLE
Michael C Baxa, Xiaoxuan Lin, Cedrick D Mukinay, Srinivas Chakravarthy, Joseph R Sachleben, Sarah Antilla, Nina Hartrampf, Joshua A Riback, Isabelle A Gagnon, Bradley L Pentelute, Patricia L Clark, Tobin R Sosnick
Despite the generally accepted role of the hydrophobic effect as the driving force for folding, many intrinsically disordered proteins (IDPs), including those with hydrophobic content typical of foldable proteins, behave nearly as self-avoiding random walks (SARWs) under physiological conditions. Here, we tested how temperature and ionic conditions influence the dimensions of the N-terminal domain of pertactin (PNt), an IDP with an amino acid composition typical of folded proteins. While PNt contracts somewhat with temperature, it nevertheless remains expanded over 10-58°C, with a Flory exponent, ν, >0...
May 2024: Protein Science
https://read.qxmd.com/read/38605029/pathogenic-mutations-of-human-phosphorylation-sites-affect-protein-protein-interactions
#28
JOURNAL ARTICLE
Trendelina Rrustemi, Katrina Meyer, Yvette Roske, Bora Uyar, Altuna Akalin, Koshi Imami, Yasushi Ishihama, Oliver Daumke, Matthias Selbach
Despite their lack of a defined 3D structure, intrinsically disordered regions (IDRs) of proteins play important biological roles. Many IDRs contain short linear motifs (SLiMs) that mediate protein-protein interactions (PPIs), which can be regulated by post-translational modifications like phosphorylation. 20% of pathogenic missense mutations are found in IDRs, and understanding how such mutations affect PPIs is essential for unraveling disease mechanisms. Here, we employ peptide-based interaction proteomics to investigate 36 disease-associated mutations affecting phosphorylation sites...
April 11, 2024: Nature Communications
https://read.qxmd.com/read/38602656/investigating-the-effects-of-perampanel-on-autophagy-mediated-regulation-of-glua2-and-psd95-in-epilepsy
#29
JOURNAL ARTICLE
Dan Li, Na Sun, Yingying Guo, Shaoping Huang, Chunyan Yin, Yanfeng Xiao, Weijun Ma
Epilepsy is a chronic neurological disorder characterized by recurrent seizures. Despite various treatment approaches, a significant number of patients continue to experience uncontrolled seizures, leading to refractory epilepsy. The emergence of novel anti-epileptic drugs, such as perampanel (PER), has provided promising options for effective epilepsy treatment. However, the specific mechanisms underlying the therapeutic effects of PER remain unclear. This study aimed to investigate the intrinsic molecular regulatory mechanisms involved in the downregulation of GluA2, a key subunit of α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid receptors, following epileptic seizures...
April 11, 2024: Molecular Neurobiology
https://read.qxmd.com/read/38600891/deep-targeted-gene-sequencing-reveals-arid1a-mutation-as-an-important-driver-of-glioblastoma
#30
JOURNAL ARTICLE
Menglin Xiao, Xiaoteng Cui, Can Xu, Lei Xin, Jixing Zhao, Shixue Yang, Biao Hong, Yanli Tan, Jie Zhang, Xiang Li, Jie Li, Chunsheng Kang, Chuan Fang
AIMS: To investigate the key factors influencing glioma progression and the emergence of treatment resistance by examining the intrinsic connection between mutations in DNA damage and repair-related genes and the development of chemoresistance in gliomas. METHODS: We conducted a comprehensive analysis of deep-targeted gene sequencing data from 228 glioma samples. This involved identifying differentially mutated genes across various glioma grades, assessing their functions, and employing I-TASSER for homology modeling...
April 2024: CNS Neuroscience & Therapeutics
https://read.qxmd.com/read/38600130/fuzzy-recognition-by-the-prokaryotic-transcription-factor-higa2-from-vibrio-cholerae
#31
JOURNAL ARTICLE
San Hadži, Zala Živič, Matic Kovačič, Uroš Zavrtanik, Sarah Haeserts, Daniel Charlier, Janez Plavec, Alexander N Volkov, Jurij Lah, Remy Loris
Disordered protein sequences can exhibit different binding modes, ranging from well-ordered folding-upon-binding to highly dynamic fuzzy binding. The primary function of the intrinsically disordered region of the antitoxin HigA2 from Vibrio cholerae is to neutralize HigB2 toxin through ultra-high-affinity folding-upon-binding interaction. Here, we show that the same intrinsically disordered region can also mediate fuzzy interactions with its operator DNA and, through interplay with the folded helix-turn-helix domain, regulates transcription from the higBA2 operon...
April 10, 2024: Nature Communications
https://read.qxmd.com/read/38598681/4-4-difluoroproline-as-a-unique-19-f-nmr-probe-of-proline-conformation
#32
JOURNAL ARTICLE
Himal K Ganguly, Brice A Ludwig, Caitlin M Tressler, Megh R Bhatt, Anil K Pandey, Caitlin M Quinn, Shi Bai, Glenn P A Yap, Neal J Zondlo
Despite the importance of proline conformational equilibria ( trans versus cis amide and exo versus endo ring pucker) on protein structure and function, there is a lack of convenient ways to probe proline conformation. 4,4-Difluoroproline (Dfp) was identified to be a sensitive 19 F NMR-based probe of proline conformational biases and cis-trans isomerism. Within model compounds and disordered peptides, the diastereotopic fluorines of Dfp exhibit similar chemical shifts (ΔδFF = 0-3 ppm) when a trans X-Dfp amide bond is present...
April 10, 2024: Biochemistry
https://read.qxmd.com/read/38598299/neurofilament-biophysics-from-structure-to-biomechanics
#33
REVIEW
Erika A Ding, Sanjay Kumar
Neurofilaments (NFs) are multi-subunit, neuron-specific intermediate filaments consisting of a 10-nm diameter filament "core" surrounded by a layer of long intrinsically disordered protein (IDP) "tails." NFs are thought to regulate axonal caliber during development and then stabilize the mature axon, with NF subunit misregulation, mutation, and aggregation featuring prominently in multiple neurological diseases. The field's understanding of NF structure, mechanics, and function has been deeply informed by a rich variety of biochemical, cell biological, and mouse genetic studies spanning more than four decades...
April 10, 2024: Molecular Biology of the Cell
https://read.qxmd.com/read/38597222/protein-misfolding-and-amyloid-nucleation-through-liquid-liquid-phase-separation
#34
REVIEW
Semanti Mukherjee, Manisha Poudyal, Kritika Dave, Pradeep Kadu, Samir K Maji
Liquid-liquid phase separation (LLPS) is an emerging phenomenon in cell physiology and diseases. The weak multivalent interaction prerequisite for LLPS is believed to be facilitated through intrinsically disordered regions, which are prevalent in neurodegenerative disease-associated proteins. These aggregation-prone proteins also exhibit an inherent property for phase separation, resulting in protein-rich liquid-like droplets. The very high local protein concentration in the water-deficient confined microenvironment not only drives the viscoelastic transition from the liquid to solid-like state but also most often nucleate amyloid fibril formation...
April 10, 2024: Chemical Society Reviews
https://read.qxmd.com/read/38597191/massive-er-protein-disposal-by-reticulophagy-receptors-and-selective-disposal-by-tollip
#35
JOURNAL ARTICLE
Yuki Hayashi, Hidenori Ichijo
Proteostasis of the endoplasmic reticulum (ER) is maintained by coordinated action of two major catabolic pathways: proteasome-dependent ER-associated degradation (ERAD) and less characterized lysosomal pathways. Recent studies on ER-specific autophagy (termed "reticulophagy") have highlighted the importance of lysosomes for ER proteostasis. Key to this process are proteins termed reticulophagy receptors that connect ER fragments and Atg8-family proteins, facilitating the lysosomal degradation of both native and aberrant ER proteins in a relatively nonselective manner...
April 10, 2024: Autophagy
https://read.qxmd.com/read/38591484/proteasome-dependent-degradation-of-histone-h1-subtypes-is-mediated-by-its-c-terminal-domain
#36
JOURNAL ARTICLE
D García-Gomis, J López, A Calderón, M Andrés, I Ponte, A Roque
Histone H1 is involved in chromatin compaction and dynamics. In human cells, the H1 complement is formed by different amounts of somatic H1 subtypes, H1.0-H1.5 and H1X. The amount of each variant depends on the cell type, the cell cycle phase, and the time of development and can be altered in disease. However, the mechanisms regulating H1 protein levels have not been described. We have analyzed the contribution of the proteasome to the degradation of H1 subtypes in human cells using two different inhibitors: MG132 and bortezomib...
May 2024: Protein Science
https://read.qxmd.com/read/38588835/order-wrapped-in-chaos-on-the-roles-of-intrinsically-disordered-proteins-and-rnas-in-the-arrangement-of-the-mitochondrial-enzymatic-machines
#37
JOURNAL ARTICLE
Semen V Nesterov, Nikolay S Ilyinsky, Konstantin S Plokhikh, Vladimir D Manuylov, Yuriy M Chesnokov, Raif G Vasilov, Irina M Kuznetsova, Konstantin K Turoverov, Valentin Ivanovich, Alexander V Fonin, Vladimir N Uversky
The analysis of cryo-electron tomography images of human and rat mitochondria revealed that the mitochondrial matrix is at least as crowded as the cytosol. To mitigate the crowding effects, metabolite transport in the mitochondria primarily occurs through the intermembrane space, which is significantly less crowded. The scientific literature largely ignores how enzyme systems and metabolite transport are organized in the crowded environment of the mitochondrial matrix. Under crowded conditions, multivalent interactions carried out by disordered protein regions (IDRs), may become extremely important...
April 6, 2024: International Journal of Biological Macromolecules
https://read.qxmd.com/read/38587193/assembly-of-sars-cov-2-nucleocapsid-protein-with-nucleic-acid
#38
JOURNAL ARTICLE
Huaying Zhao, Abdullah M Syed, Mir M Khalid, Ai Nguyen, Alison Ciling, Di Wu, Wai-Ming Yau, Sanjana Srinivasan, Dominic Esposito, Jennifer A Doudna, Grzegorz Piszczek, Melanie Ott, Peter Schuck
The viral genome of SARS-CoV-2 is packaged by the nucleocapsid (N-)protein into ribonucleoprotein particles (RNPs), 38 ± 10 of which are contained in each virion. Their architecture has remained unclear due to the pleomorphism of RNPs, the high flexibility of N-protein intrinsically disordered regions, and highly multivalent interactions between viral RNA and N-protein binding sites in both N-terminal (NTD) and C-terminal domain (CTD). Here we explore critical interaction motifs of RNPs by applying a combination of biophysical techniques to ancestral and mutant proteins binding different nucleic acids in an in vitro assay for RNP formation, and by examining nucleocapsid protein variants in a viral assembly assay...
April 8, 2024: Nucleic Acids Research
https://read.qxmd.com/read/38585848/serbp1-interacts-with-parp1-and-is-present-in-parylation-dependent-protein-complexes-regulating-splicing-cell-division-and-ribosome-biogenesis
#39
Kira Breunig, Xiufen Lei, Mauro Montalbano, Gabriela D A Guardia, Shiva Ostadrahimi, Victoria Alers, Adam Kosti, Jennifer Chiou, Nicole Klein, Corina Vinarov, Lily Wang, Mujia Li, Weidan Song, W Lee Kraus, David S Libich, Stefano Tiziani, Susan T Weintraub, Pedro A F Galante, Luiz O F Penalva
RNA binding proteins (RBPs) containing intrinsically disordered regions (IDRs) are present in diverse molecular complexes where they function as dynamic regulators. Their characteristics promote liquid-liquid phase separation (LLPS) and the formation of membraneless organelles such as stress granules and nucleoli. IDR-RBPs are particularly relevant in the nervous system and their dysfunction is associated with neurodegenerative diseases and brain tumor development. SERBP1 is a unique member of this group, being mostly disordered and lacking canonical RNA-binding domains...
March 25, 2024: bioRxiv
https://read.qxmd.com/read/38585827/junctional-adhesion-molecule-jam-c-recruitment-of-pard3-and-drebrin-to-cell-contacts-initiates-neuron-glia-recognition-and-layer-specific-cell-sorting-in-developing-cerebella
#40
Liam P Hallada, Abbas Shirinifard, David J Solecki
Sorting maturing neurons into distinct layers is critical for brain development, with disruptions leading to neurological disorders and pediatric cancers. Lamination coordinates where, when, and how cells interact, facilitating events that direct migrating neurons to their destined positions within emerging neural networks and control the wiring of connections in functional circuits. While the role of adhesion molecule expression and presentation in driving adhesive recognition during neuronal migration along glial fibers is recognized, the mechanisms by which the spatial arrangement of these molecules on the cell surface dictates adhesive specificity and translates contact-based external cues into intracellular responses like polarization and cytoskeletal organization remain largely unexplored...
March 29, 2024: bioRxiv
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