Relevant bibliographies by topics / Intracellular protein

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Intracellular protein'

Author: Grafiati
Published: 3 June 2025
Last updated: 31 July 2025

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Journal articles on the topic "Intracellular protein"

1

Zettergren, Lennart. "INTRACELLULAR PROTEIN CRYSTALLISATION." Acta Pathologica Microbiologica Scandinavica 36, no. 4 (2009): 316–22. http://dx.doi.org/10.1111/j.1699-0463.1955.tb04621.x.

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Zettergren, Lennart. "INTRACELLULAR PROTEIN CRYSTALLIZATION." Acta Pathologica Microbiologica Scandinavica 26, no. 5 (2009): 696–704. http://dx.doi.org/10.1111/j.1699-0463.1949.tb00770.x.

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Vella, F. "Intracellular protein degradation." Biochemical Education 21, no. 1 (1993): 52. http://dx.doi.org/10.1016/0307-4412(93)90027-w.

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Hipkiss, A. R. "Intracellular protein degradation." FEBS Letters 323, no. 3 (1993): 298. http://dx.doi.org/10.1016/0014-5793(93)81367-9.

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Singh, Arunima. "Intracellular protein editing." Nature Methods 22, no. 6 (2025): 1128. https://doi.org/10.1038/s41592-025-02734-y.

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Beynon, R. J., and J. S. Bond. "Catabolism of intracellular protein: molecular aspects." American Journal of Physiology-Cell Physiology 251, no. 2 (1986): C141—C152. http://dx.doi.org/10.1152/ajpcell.1986.251.2.c141.

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All living cells regulate the content and composition of their resident proteins, but the mechanisms by which this is accomplished are not understood. The process of protein degradation has an important role in determining steady state and fluctuations of protein concentrations in mammalian cells. This process may be regulated by innate properties of the protein substrates, by factors that interact or "brand" proteins for degradation or by the degradative machinery of the cell. For a specific protein, there appears to be a committed step, an irreversible event that leads to rapid and extensive
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Benn, Jonathan, Shi Cheng, Sophie Keeling, et al. "Aggregate-selective removal of pathological tau by clustering-activated degraders." Science 385, no. 6712 (2024): 1009–16. http://dx.doi.org/10.1126/science.adp5186.

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Selective degradation of pathological protein aggregates while sparing monomeric forms is of major therapeutic interest. The E3 ligase tripartite motif–containing protein 21 (TRIM21) degrades antibody-bound proteins in an assembly state–specific manner due to the requirement of TRIM21 RING domain clustering for activation, yet effective targeting of intracellular assemblies remains challenging. Here, we fused the RING domain of TRIM21 to a target-specific nanobody to create intracellularly expressed constructs capable of selectively degrading assembled proteins. We evaluated this approach agai
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Miersch, Shane, and Sachdev S. Sidhu. "Intracellular targeting with engineered proteins." F1000Research 5 (August 10, 2016): 1947. http://dx.doi.org/10.12688/f1000research.8915.1.

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If the isolation, production, and clinical use of insulin marked the inception of the age of biologics as therapeutics, the convergence of molecular biology and combinatorial engineering techniques marked its coming of age. The first wave of recombinant protein-based drugs in the 1980s demonstrated emphatically that proteins could be engineered, formulated, and employed for clinical advantage. Yet despite the successes of protein-based drugs such as antibodies, enzymes, and cytokines, the druggable target space for biologics is currently restricted to targets outside the cell. Insofar as estim
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Kwaik, Yousef Abu. "Induced Expression of the Legionella pneumophila Gene Encoding a 20-Kilodalton Protein during Intracellular Infection." Infection and Immunity 66, no. 1 (1998): 203–12. http://dx.doi.org/10.1128/iai.66.1.203-212.1998.

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ABSTRACT The eukaryotic protein synthesis inhibitor cycloheximid has been used by many investigators to selectively radiolabel intracellular bacteria. Although cycloheximide has no direct effect on bacterial gene expression, there are concerns that long-term inhibition of the host cell protein synthesis may have secondary effects on bacterial gene expression. Therefore, prior to further identification and cloning of the macrophage-induced (MI) genes of Legionella pneumophila, the effects of cycloheximide on L. pneumophila-infected U937 cells were evaluated by transmission electron microscopy.
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Tani, Katsuko, Takeshi Kogure, and Hiroki Inoue. "The intracellular phospholipase A1 protein family." BioMolecular Concepts 3, no. 5 (2012): 471–78. http://dx.doi.org/10.1515/bmc-2012-0014.

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AbstractPhospholipase A1 is an enzyme that hydrolyzes phospholipids, producing 2-acyl-lysophospholipids and fatty acids. The intracellular phospholipase A1 (iPLA1) protein family is a relatively recently discovered lipid-metabolizing enzyme family. Lower eukaryotes, such as yeasts and nematodes, and plants have only one iPLA1 protein, whereas mammals have three iPLA1 family proteins (PA-PLA1/DDHD1/iPLA1α, p125/Sec23IP/iPLA1β and KIAA0725p/DDHD2/iPLA1γ). Mammalian iPLA1 proteins are localized in different cellular compartments, and two of them, p125 and KIAA0725p, have been implicated in membra
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Dissertations / Theses on the topic "Intracellular protein"

1

Villar, i. Piqué Anna. "Characterization of intracellular protein aggregates." Doctoral thesis, Universitat Autònoma de Barcelona, 2013. http://hdl.handle.net/10803/120241.

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Durant les últimes dècades, l'agregació de proteïnes ha esdevingut un tema d’investigació molt dinàmic que s'estén transversalment per diferents camps de recerca, incloent la bioquímica, la biotecnologia, la biomedicina i la nanotecnologia. D'una banda, l'acumulació de proteïnes en dipòsits amiloids insolubles constitueix una característica comuna de molts trastorns humans, coneguts com a malalties conformacionals. D'altra banda, des d'un punt de vista biotecnològic, l’agregació proteica representa un obstacle habitual en la producció de proteïnes recombinants, que en general s'acumulen en for
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Nair, Prashant. "Signals involved in protein intracellular sorting /." Basel : [s.n.], 2005. http://edoc.unibas.ch/diss/DissB_6999.

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Selivanova, Alexandra. "Intracellular dynamics of Alzheimer disease-related proteins /." Stockholm, 2007. http://diss.kib.ki.se/2007/978-91-7357-234-7/.

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Bowerman, Peter A. "Exploring protein interactions and intracellular localization in regulating flavonoid metabolism." Diss., Virginia Tech, 2010. http://hdl.handle.net/10919/77174.

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The organization of biological processes via protein-protein interactions and the subcellular localization of enzymes is believed to be fundamental to many aspects of metabolism. Although this organization has been demonstrated in several systems, the mechanisms by which it is established and regulated are still not well understood. The flavonoid biosynthetic pathway offers a unique system in which to study several important aspects of metabolism. Here we describe a novel toolset of mutant alleles within the flavonoid biosynthetic pathway. In addition, we discuss the use of several of these al
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Deme, Justin. "Protein-protein interactions for early intracellular vitamin B12 metabolism in mammals." Thesis, McGill University, 2014. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=123014.

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Vitamin B12, or cobalamin, is a water soluble vitamin required as cofactor for two mammalian enzymatic processes: homocysteine remethylation to methionine in the cytoplasm using methionine synthase (MS), and fatty acid/amino acid metabolism in the mitochondrion using methylmalonyl-CoA mutase (MCM). Whereas the molecular nature of intracellular cobalamin metabolism in mammals remains poorly understood, the proteins MMACHC, MMADHC, LMBD1 and ABCD4 are implicated in its early uptake and processing. Due to the inherent challenges associated with the cellular utilization of cobalamin, we propose th
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COSTA, B. G. FIGUEIREDO. "'INTRACELLULAR TARGETING OF TAIL-ANCHORED PROTEINS'." Doctoral thesis, Università degli Studi di Milano, 2017. http://hdl.handle.net/2434/468362.

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Tail-anchored (TA) proteins constitute a class of membrane proteins whose diverse members carry out basic functions in cell physiology, including regulation of exocytosis and of apoptosis. TA proteins share a particular topology, consisting in a cytosolically located N-terminal domain anchored to the bilayer by a C-terminal hydrophobic stretch. Because of this particular topology, these proteins are targeted to their destination by unique post-translational pathways. An important identified pathway is centred on the ATPase TRC40/Get3, however, at least under cell-free conditions, some TA prote
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游, 晧欣. "Development of novel systems promoting intracellular protein delivery." 京都大学 (Kyoto University), 2012. http://hdl.handle.net/2433/157905.

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Walker, Simon W. "Studies on the intracellular calcium-binding protein calmodulin." Thesis, University of Oxford, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.235957.

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Brawn, Lyndsey Claire. "A Salmonella invasion protein essential for intracellular replication." Thesis, University of Cambridge, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.613308.

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Chen, Jinyun. "REGULATION OF INTRACELLULAR ARYL HYDROCARBON RECEPTOR PROTEIN LEVELS." Scholarly Commons, 2020. https://scholarlycommons.pacific.edu/uop_etds/3675.

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The aryl hydrocarbon receptor (AHR) is a ligand-activated signaling molecule which controls tumor growth and metastasis, T cell differentiation, and liver development. Expression levels of this receptor protein are sensitive to the cellular p23 protein levels in immortalized cancer cell lines. As little as 30% reduction of the p23 cellular content can suppress the AHR function. Here we reported that down-regulation of the p23 protein content in normal, untransformed human bronchial/tracheal epithelial cells to 48% of its content also suppresses the AHR protein levels to 54% of its content. Thi
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Books on the topic "Intracellular protein"

1

Doherty, Fergus J. Intracellular protein degradation. IRL Press, 1992.

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Suzuki, Koichi, and Judith S. Bond, eds. Intracellular Protein Catabolism. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0335-0.

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1924-, Suzuki Koichi, Bond Judith S, and International Symposium on Intracellular Protein Catabolism (10th : 1994 : Tokyo, Japan), eds. Intracellular protein catabolism. Plenum Press, 1996.

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Verner, Keith. Intracellular protein transport and membrane biogenesis. R.G. Landes Company, 1995.

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International Symposium on Intracellular Protein Catabolism (6th 1986 Büchenberg (Magdeburg, Germany)). Intracellular protein catabolism: Abstracts of the 6th symposium. Edited by Aurich H, Kirschke Heidrun, Wiederanders Bernd, Proteolysis Group in Halle, and Biochemische Gesellschaft der Deutschen Demokratischen Republik. Martin-Luther-Universität Halle-Wittenberg, 1986.

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Horn, Justin Michael. Engineering Stimuli-Responsive Protein Phase Separations for Protein Stabilization, Modulation of Protein Activity, and Intracellular Protein Delivery. [publisher not identified], 2022.

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Hugosson, Marie. Intracellular protein transport in plants: Targeting, sorting and processing. Stockholm University, 1996.

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Wilks, Andrew F. Intracellular signal transduction: The JAK-STAT pathway. Springer, 1996.

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9

A, Khairallah Edward, Bond Judith S, and Bird John W. C, eds. Intracellular protein catabolism: Proceedings of the Fifth International Symposium on Intracellular Protein Catabolism, held May 29-June 2, 1984, at the Airlie Conference Center, Airlie, Virginia. A.R. Liss, 1985.

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Mao, De Yu. Chloride Intracellular Channel (CLIC) proteins function to modulate Rac1 and RhoA downstream of endothelial G-protein coupled receptors signaling. [publisher not identified], 2019.

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Book chapters on the topic "Intracellular protein"

1

Bode, W., F. Grams, P. Reinemer, et al. "The Metzincin-Superfamily of Zinc-Peptidases." In Intracellular Protein Catabolism. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0335-0_1.

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Järvinen, M., N. Kalkkinen, A. Rinne, and V. K. Hopsu-Havu. "The 43 kDa Papain-Inhibiting Protein in Psoriatic Epidermis is Identical to Squamous Cell Carcinoma Antigen (SCC-Antigen)." In Intracellular Protein Catabolism. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0335-0_10.

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Wang, Kevin K. W., Avigail Posner, Kadee J. Raser, et al. "Alpha-Mercaptoacrylic Acid Derivatives as Novel Selective Calpain Inhibitors." In Intracellular Protein Catabolism. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0335-0_11.

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Seglen, Per O., Trond Olav Berg, Henrietta Blankson, Monica Fengsrud, Ingunn Holen, and Per Eivind Strømhaug. "Structural Aspects of Autophagy." In Intracellular Protein Catabolism. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0335-0_12.

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Kadowaki, Motoni, Rina Venerando, Giovanni Miotto, and Glenn E. Mortimore. "Mechanism of Autophagy in Permeabilized Hepatocytes." In Intracellular Protein Catabolism. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0335-0_13.

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Ezaki, J., L. S. Wolfe, K. Ishidoh, D. Muno, T. Ueno, and E. Kominami. "Lysosomal Proteinosis Based on Decreased Degration of a Specific Protein, Mitochondrial ATP Synthase Subunit C." In Intracellular Protein Catabolism. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0335-0_14.

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Palmer, D. N., and J. M. Hay. "The Neuronal Ceroid Lipofuscinoses (Batten Disease)." In Intracellular Protein Catabolism. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0335-0_15.

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Suzuki, Toshiaki, Kozo Nishiyama, Tsuneyoshi Funai, Keiji Tanaka, Akira Ichihara, and Arata Ichiyama. "Energy-Dependent Degration of a Mutant Serine:Pyruvate/Alanin: Glyoxylate Aminotransferase in a Primary Hyperoxaluria Type 1 C." In Intracellular Protein Catabolism. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0335-0_16.

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Turner, A. J., L. J. Murphy, M. S. Medeiros, and K. Barnes. "Endopeptidase-24.11 (Neprilysin) and Relatives." In Intracellular Protein Catabolism. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0335-0_17.

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Hayashi, M., M. Inomata, and S. Kawashima. "Function of Calpains." In Intracellular Protein Catabolism. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4613-0335-0_18.

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Conference papers on the topic "Intracellular protein"

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Wang, Lei G. "Novel fluorophores for precision quantitative imaging." In Optical Molecular Probes, Imaging and Drug Delivery. Optica Publishing Group, 2025. https://doi.org/10.1364/omp.2025.otu3e.3.

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I will present the design and development of our water-soluble, cell-permeable fluorophores that are biologically compatible and environmentally inert, enabling accurate, quantitative imaging of intracellular drug distribution and protein binding in live cells and tissues for precision imaging applications.
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Cheung, K. H., H. Y. Lai, and Ji-Dong Gu. "Reduction of Chromate by Marine Bacillus Megaterium TKW3." In CORROSION 2006. NACE International, 2006. https://doi.org/10.5006/c2006-06521.

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abstract Hexavalent chromium (Cr6+) is an important corrosion inhibitor and is also highly toxic pollutant, which can be detoxified and precipitated through reduction to Cr3+. Bacillus megaterium TKW3 isolated from contaminated sediments was capable of reducing Cr6+ in concomitance with metalloids (Se4+, Se6+ and As5+). Notwithstanding the approximately 50% inhibition, it is firstly reported that bacteria reduced Cr6+ and Se4+ [to elemental Se] simultaneously. No significant difference was observed among electron donors (glucose, maltose and mannitol) on Cr6+ reduction of B. megaterium TKW3. T
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Van holsbeeck, Kevin, Baptiste Fischer, Simon Gonzalez, et al. "Downsizing Nanobodies: Towards CDR Loop Mimetics Modulating Intracellular Protein-Protein Interactions." In 36th European Peptide Symposium. The European Peptide Society, 2022. http://dx.doi.org/10.17952/36eps.2022.141.

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Van holsbeeck, Kevin, Baptiste Fischer Fischer, Simon Gonzalez, et al. "Downsizing Nanobodies: Towards CDR Loop Mimetics Modulating Intracellular Protein-Protein Interactions." In 36th European Peptide Symposium. The European Peptide Society, 2022. http://dx.doi.org/10.17952/36eps/36eps.2022.141.

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Nawroth, Peter P., Jerry Brett, Susan Steinberg, Charles T. Esmon, and David M. Stern. "ENDOTHELIUM AND PROTEIN S: SYNTHESIS, RELEASE AND REGULATION OF ANTICOAGULANT ACTIVITY." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642962.

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The protein C-protein S pathway is closely linked to the vessel wall. In terms of protein C, endothelium has been shown to provide the receptor thrombomodulin, which promotes thrombin-mediated formation of activated protein C. Optimal anticoagulant function of activated protein C requires protein S and a cellular surface. Recent studies have indicated that endothelium can facilitate assembly of the activated protein C-protein S complex and that bovine endothelium expresses specific binding site(s) for protein S which promote its anticoagulant function. Expression of protein S binding sites is
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Akkerman, JW N. "INTRACELLULAR PH CHANGES AND PLATELET ACTIVATION." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644774.

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It is long known that platelet aggregation and secretion are accompanied by acidification of the extracellular medium. Much of the proton extrusion results from hydrolysis of ATP generated in the glycolytic pathway and liberation of secretion granules, which are slightly acidic. Recent eyidence points at a third source for extracellular protons.Following early observations (1) that epinephrine-induced platelet functions depended on extracellular Na+ (Na+ o ), it became evident that platelets possess a Na+ /H+ antiport, which regulates the cytosolic pH (pH.) via stochiometric exchange of intrac
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Awazu, K., and S. Suzuki. "Intracellular protein mass spectroscopy using mid-infrared laser ionization." In European Conference on Biomedical Optics. OSA, 2007. http://dx.doi.org/10.1364/ecbo.2007.6628_49.

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Awazu, K., and S. Suzuki. "Intracellular protein mass spectroscopy using mid-infrared laser ionization." In European Conference on Biomedical Optics, edited by Dietrich Schweitzer and Maryann Fitzmaurice. SPIE, 2007. http://dx.doi.org/10.1117/12.727753.

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Choi, Youngsil, Seulmee Shin, Kuysook Lee, and Daewoong Jo. "Abstract LB-006: Intracellular protein therapy with SOCS3 utilizing aMTD-enabled macromolecule intracellular transduction technology (MITT)." In Proceedings: AACR Annual Meeting 2018; April 14-18, 2018; Chicago, IL. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1538-7445.am2018-lb-006.

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Freeman, Eric, Lisa Mauck Weiland, and Wilson S. Meng. "Computational Study of Inclusion Burst via the Proton Sponge Hypothesis." In ASME 2010 Conference on Smart Materials, Adaptive Structures and Intelligent Systems. ASMEDC, 2010. http://dx.doi.org/10.1115/smasis2010-3756.

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Biological proteins embedded in either a biological or an engineered membrane will actively maintain electrochemical balance across that membrane through transport of fluid and charge. While membrane studies are often planar, in nature they typically take the form of inclusions (∼spherical). Study and ultimately manipulation of the protein transporter types and density, and interior/exterior states of these inclusions lend insight into burst mechanisms appropriate to a broad array of engineering and biological applications, such as intracellular burst release of a vaccine. To explore these phe
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Reports on the topic "Intracellular protein"

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Wang, Pin. Intracellular Protein Delivery for Treating Breast Cancer. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada609954.

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Wang, Pin. Intracellular Protein Delivery for Treating Breast Cancer. Defense Technical Information Center, 2014. http://dx.doi.org/10.21236/ada613760.

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Tang, Yi. Intracellular Protein Delivery for Treating Breast Cancer. Defense Technical Information Center, 2012. http://dx.doi.org/10.21236/ada564531.

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Tang, Yi. Intracellular Protein Delivery for treating Breast Cancer. Defense Technical Information Center, 2013. http://dx.doi.org/10.21236/ada585122.

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Wang, Pin. Intracellular Protein Delivery for Treating Breast Cancer. Defense Technical Information Center, 2013. http://dx.doi.org/10.21236/ada585133.

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Scavuzzo, Sebastian, Jonathan Cedeño, and Jaroslava Miksovska. In Silico Calculation of Interhelical Angles in NCS1. Florida International University, 2025. https://doi.org/10.25148/fiuurj.3.1.16.

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Proteins are important macromolecules responsible for a variety of processes in living organisms. One of the most important features of proteins is their ability to respond to environmental stimuli, such as changes in intracellular metal concentration by binding metal ions, which in turns triggers structural changes within the protein that can modify its function or allow the protein to participate in a signaling pathway. One such signaling protein is the so-called neuronal calcium sensor 1 protein or NCS1, which binds Ca2+ along with other abiogenic metals such as Li+, and the metal binding r
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Cohick, Wendie S. Phosphorylation of Intracellular IGF Binding Protein-3 by the IGF Signaling Cascade is Essential for Its Growth-Enhancing in Mammary Epithelial. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada429625.

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Avni, Adi, and Gitta L. Coaker. Proteomic investigation of a tomato receptor like protein recognizing fungal pathogens. United States Department of Agriculture, 2015. http://dx.doi.org/10.32747/2015.7600030.bard.

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Maximizing food production with minimal negative effects on the environment remains a long-term challenge for sustainable food production. Microbial pathogens cause devastating diseases, minimizing crop losses by controlling plant diseases can contribute significantly to this goal. All plants possess an innate immune system that is activated after recognition of microbial-derived molecules. The fungal protein Eix induces defense responses in tomato and tobacco. Plants recognize Eix through a leucine-rich-repeat receptor- like-protein (LRR-RLP) termed LeEix. Despite the knowledge obtained from
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Cohick, Wendie S. Phosphorylation of Intracellular IGF Binding Protein-3 by the IGF Signaling Cascade is Essential for Its Growth-Enhancing Effect in Mammary Epithelial Cells. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada409764.

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Cohick, Wendie S. Phosphorylation of Intracellular IGF Binding Protein-3 by the IGF Signaling Cascade is Essential for its Growth-Enhancing Effect in Mammary Epithelial Cells. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada418987.

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