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Relevant bibliographies by topics / Multiprotein complexes

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Academic literature on the topic 'Multiprotein complexes'

Author: Grafiati

Published: 4 June 2021

Last updated: 31 January 2023

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Journal articles on the topic "Multiprotein complexes"

1

Wolberger, Cynthia. "MULTIPROTEIN-DNA COMPLEXES IN TRANSCRIPTIONAL REGULATION." Annual Review of Biophysics and Biomolecular Structure 28, no. 1 (1999): 29–56. http://dx.doi.org/10.1146/annurev.biophys.28.1.29.

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Wiederstein, Markus, Markus Gruber, Karl Frank, Francisco Melo, and Manfred J. Sippl. "Structure-Based Characterization of Multiprotein Complexes." Structure 22, no. 7 (2014): 1063–70. http://dx.doi.org/10.1016/j.str.2014.05.005.

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Robinson, C. V. "Mass Spectrometry Characterization of Multiprotein Complexes." Cold Spring Harbor Protocols 2009, no. 3 (2009): pdb.prot5180. http://dx.doi.org/10.1101/pdb.prot5180.

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Gammons, Melissa, and Mariann Bienz. "Multiprotein complexes governing Wnt signal transduction." Current Opinion in Cell Biology 51 (April 2018): 42–49. http://dx.doi.org/10.1016/j.ceb.2017.10.008.

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Rothan, Hussin A., and Mukesh Kumar. "Role of Endoplasmic Reticulum-Associated Proteins in Flavivirus Replication and Assembly Complexes." Pathogens 8, no. 3 (2019): 148. http://dx.doi.org/10.3390/pathogens8030148.

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Flavivirus replication in host cells requires the formation of replication and assembly complexes on the cytoplasmic side of the endoplasmic reticulum (ER) membrane. These complexes consist of an ER membrane, viral proteins, and host proteins. Genome-wide investigations have identified a number of ER multiprotein complexes as vital factors for flavivirus replication. The detailed mechanisms of the role of ER complexes in flavivirus replication are still largely elusive. This review highlights the fact that the ER multiprotein complexes are crucial for the formation of flavivirus replication an

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Thompson, Andrea D., Amanda Dugan, Jason E. Gestwicki, and Anna K. Mapp. "Fine-Tuning Multiprotein Complexes Using Small Molecules." ACS Chemical Biology 7, no. 8 (2012): 1311–20. http://dx.doi.org/10.1021/cb300255p.

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Kim, R. "Native Agarose Gel Electrophoresis of Multiprotein Complexes." Cold Spring Harbor Protocols 2011, no. 7 (2011): pdb.prot4558. http://dx.doi.org/10.1101/pdb.prot4558.

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Berger, Imre, Daniel J. Fitzgerald, and Timothy J. Richmond. "Baculovirus expression system for heterologous multiprotein complexes." Nature Biotechnology 22, no. 12 (2004): 1583–87. http://dx.doi.org/10.1038/nbt1036.

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Kusch, Thomas, Sebastián Guelman, Susan M. Abmayr, and Jerry L. Workman. "Two Drosophila Ada2 Homologues Function in Different Multiprotein Complexes." Molecular and Cellular Biology 23, no. 9 (2003): 3305–19. http://dx.doi.org/10.1128/mcb.23.9.3305-3319.2003.

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ABSTRACT The reversible acetylation of the N-terminal tails of histones is crucial for transcription, DNA repair, and replication. The enzymatic reaction is catalyzed by large multiprotein complexes, of which the best characterized are the Gcn5-containing N-acetyltransferase (GNAT) complexes. GNAT complexes from yeast to humans share several conserved subunits, such as Ada2, Ada3, Spt3, and Tra1/TRRAP. We have characterized these factors in Drosophila and found that the flies have two distinct Ada2 variants (dAda2a and dAda2b). Using a combination of biochemical and cell biological approaches

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Donowitz, Mark, and Xuhang Li. "Regulatory Binding Partners and Complexes of NHE3." Physiological Reviews 87, no. 3 (2007): 825–72. http://dx.doi.org/10.1152/physrev.00030.2006.

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NHE3 is the brush-border (BB) Na+/H+ exchanger of small intestine, colon, and renal proximal tubule which is involved in large amounts of neutral Na+ absorption. NHE3 is a highly regulated transporter, being both stimulated and inhibited by signaling that mimics the postprandial state. It also undergoes downregulation in diarrheal diseases as well as changes in renal disorders. For this regulation, NHE3 exists in large, multiprotein complexes in which it associates with at least nine other proteins. This review deals with short-term regulation of NHE3 and the identity and function of its recog

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Dissertations / Theses on the topic "Multiprotein complexes"

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Beer, Monika. "Analysis of Multiprotein Complexes in the Mammalian REtina." Diss., lmu, 2008. http://nbn-resolving.de/urn:nbn:de:bvb:19-95324.

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Satchwell, Timothy James. "Trafficking and assembly of band 3 based multiprotein complexes during erythropoiesis." Thesis, University of Bristol, 2011. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.556746.

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The work presented in this thesis has developed an existing in vitro culture system used for expansion of cord blood progenitors to one that can be applied to expand significant numbers of erythroblasts from peripheral blood mononuclear cells isolated from healthy donor blood samples or patients with haemolytic anaemia. These erythroblasts can be further differentiated to enucleated reticulocytes synchronously producing homogeneous populations of cells at each of the morphologically defined stages of erythroid differentiation in quantities amenable to biochemical experimentation. Expression pr

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Hanssen-Bauer, Audun. "X-ray repair cross-complementing protein 1 associated multiprotein complexes in base excision repair." Doctoral thesis, Norges teknisk-naturvitenskapelige universitet, Institutt for kreftforskning og molekylær medisin, 2012. http://urn.kb.se/resolve?urn=urn:nbn:no:ntnu:diva-16986.

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XRCC1 assoierte multiproteinkomplekser i base eksisjonsreparasjon Arvestoffet (DNA) degraderes konstant av ytre faktorer, som stråling og kjemikalier, og indre faktorer, som produkter av metabolismen. Slik degradering ødelegger informasjonen som ligger i DNA, og kan derfor være toksisk for cellene og mutagent under replikasjon. Sannsynligheten for mutasjon er likevel ekstremt lav fordi DNAets integritet opprettholdes ved en lang rekke reparasjonsmekanismer. Disse involverer mange enzymer, struktur- og regulatoriske proteiner, med overlappende roller. Feil eller mangelfull reparasjon er drivkr

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Spindler, Marie-Christin [Verfasser], Ricardo [Gutachter] Benavente, and Markus [Gutachter] Sauer. "Molecular architecture of meiotic multiprotein complexes / Marie-Christin Spindler ; Gutachter: Ricardo Benavente, Markus Sauer." Würzburg : Universität Würzburg, 2020. http://d-nb.info/1218973242/34.

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Doughty, Tyler W. "Levels of YCG1 Limit Condensin Function during the Cell Cycle: A Dissertation." eScholarship@UMMS, 2016. https://escholarship.umassmed.edu/gsbs_diss/861.

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For nearly five decades, the simple eukaryote Saccharomyces cerevisiae has been used as a model for understanding the eukaryotic cell cycle. One vein of this research has focused on understanding how chromosome structure is regulated in relation to the cell cycle. This work characterizes a new mechanism that modulates the chromatin organizing condensin complex, in hopes of furthering the understanding of chromosome structure regulation in eukaryotes. During mitosis, chromosomes are condensed to facilitate their segregation through a process mediated by the condensin complex. Upon interphase on

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Doughty, Tyler W. "Levels of YCG1 Limit Condensin Function during the Cell Cycle: A Dissertation." eScholarship@UMMS, 2008. http://escholarship.umassmed.edu/gsbs_diss/861.

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For nearly five decades, the simple eukaryote Saccharomyces cerevisiae has been used as a model for understanding the eukaryotic cell cycle. One vein of this research has focused on understanding how chromosome structure is regulated in relation to the cell cycle. This work characterizes a new mechanism that modulates the chromatin organizing condensin complex, in hopes of furthering the understanding of chromosome structure regulation in eukaryotes. During mitosis, chromosomes are condensed to facilitate their segregation through a process mediated by the condensin complex. Upon interphase on

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Legen, Juliana. "Gene expression in plastids of higher plants: evolutionary and functional aspects of different RNA polymerases - coordinated assembly of multiprotein-complexes." Diss., lmu, 2003. http://nbn-resolving.de/urn:nbn:de:bvb:19-9739.

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Adelman, Carrie A. "Analysis of Mre11 complex roles : in response to physiological sources of DNA damage in the mouse /." Access full-text from WCMC, 2009. http://proquest.umi.com/pqdweb?did=1619067681&sid=1&Fmt=2&clientId=8424&RQT=309&VName=PQD.

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Hazra, Ditipriya. "Insights into the control of mRNA decay by YTH proteins during the transition from meiosis to mitosis in yeasts." Thesis, Université Paris-Saclay (ComUE), 2019. http://www.theses.fr/2019SACLX041.

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Aperçu du contrôle de la dégradation des ARNm par les protéines YTHpendant la transition de la méiose à la mitose chez les levures.Le cycle cellulaire est contrôlé par des processus complexes et interconnectés. Un gène est transcrit en ARNm qui est traduit en protéines mais de nombreux processus de régulation travaillent pour contrôler chaque étape de ce processus apparemment simple. Parmi ces points de contrôle, la régulation post-transcriptionnelle est importante, et la formation d'un complexe protéine-ARN peut diriger le destin cellulaire. Parmi ces protéines de liaison à l'ARN, les protéin

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Driscoll, David R. "The Impact of mTORC2 Signaling on the Initiation and Progression of KRAS-Driven Pancreatic Neoplasias: A Dissertation." eScholarship@UMMS, 2016. https://escholarship.umassmed.edu/gsbs_diss/821.

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Pancreatic ductal adenocarcinoma (PDAC), the most common form of pancreatic cancer, develops through progression of premalignant pancreatic intraepithelial neoplasias (PanINs). In mouse-models, KRAS-activation in acinar cells induced an acinar-to-ductal metaplasia (ADM), and mutation of the Kras oncogene is believed to initiate PanIN formation. ADM is also promoted by pancreatic injury, which cooperates with activated KRAS to stimulate PanIN and PDAC formation from metaplastic ducts. Our lab, and others, have shown that the downstream PI3K/AKT pathway is important for KRAS-mediated proliferati

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Books on the topic "Multiprotein complexes"

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Poterszman, Arnaud, ed. Multiprotein Complexes. Springer US, 2021. http://dx.doi.org/10.1007/978-1-0716-1126-5.

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Protein-protein complexes: Analysis, modeling and drug design. Imperial College Press, 2010.

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Poterszman, Arnaud. Multiprotein Complexes: Methods and Protocols. Springer, 2020.

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Poterszman, Arnaud. Multiprotein Complexes: Methods and Protocols. Springer, 2021.

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Zacharias, Martin. Protein-Protein Complexes: Analysis, Modeling and Drug Design. World Scientific Publishing Co Pte Ltd, 2010.

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The Eukaryotic Replisome A Guide To Protein Structure And Function. Springer, 2012.

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Book chapters on the topic "Multiprotein complexes"

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Kurochkina, Natalya. "Multiprotein Complexes." In Protein Structure and Modeling. Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-6601-7_6.

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Vaquero, Alejandro, Michael Scher, and Danny Reinberg. "Biochemistry of Multiprotein HDAC Complexes." In Histone Deacetylases. Humana Press, 2006. http://dx.doi.org/10.1385/1-59745-024-3:23.

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Wang, Yuan-Liang, Francesco Faiola, and Ernest Martinez. "Purifi cation of Multiprotein Histone Acetyltransferase Complexes." In Methods in Molecular Biology. Springer New York, 2011. http://dx.doi.org/10.1007/978-1-61779-376-9_28.

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Shevchenko, Andrej, and Matthias Mann. "Deciphering Functionally Important Multiprotein Complexes by Mass Spectrometry." In Mass Spectrometry in Biology & Medicine. Humana Press, 2000. http://dx.doi.org/10.1007/978-1-59259-719-2_14.

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Dhamija, Sonam, and Manoj B. Menon. "Long Noncoding RNAs as Scaffolds for Multiprotein Signaling Complexes." In RNA Technologies. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-44743-4_5.

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Schuck, Peter. "Sedimentation Velocity in the Study of Reversible Multiprotein Complexes." In Protein Interactions. Springer US, 2007. http://dx.doi.org/10.1007/978-0-387-35966-3_16.

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Lasserre, Jean Paul, and Armelle Ménard. "Two-Dimensional Blue Native/SDS Gel Electrophoresis of Multiprotein Complexes." In Methods in Molecular Biology. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-821-4_27.

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Andrès, Charles, Birgit Agne, and Felix Kessler. "Preparation of Multiprotein Complexes from Arabidopsis Chloroplasts Using Tandem Affinity Purification." In Chloroplast Research in Arabidopsis. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-237-3_3.

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Abdulrahman, Wassim, Laura Radu, Frederic Garzoni, et al. "The Production of Multiprotein Complexes in Insect Cells Using the Baculovirus Expression System." In Methods in Molecular Biology. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-2230-7_5.

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Paro, Renato, Ueli Grossniklaus, Raffaella Santoro, and Anton Wutz. "Cellular Memory." In Introduction to Epigenetics. Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-68670-3_3.

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AbstractThe identity of cells in an organism is largely defined by their specific transcriptional profile. During cell division, these profiles need to be faithfully inherited to the daughter cells to ensure the maintenance of cell structure and function in a cell lineage. Here, you will learn how two groups of chromatin regulators, the Polycomb group (PcG) and the Trithorax group (TrxG), act in an antagonistic manner to maintain differential gene expression states. Members of the PcG cooperate in large multiprotein complexes to modify histones with repressive marks, resulting in condensed chromatin domains. Conversely, the TrxG proteins counteract the repressed domains by opening nucleosomal structures and establishing activating histone modifications. PcG and TrxG proteins are evolutionary highly conserved and control diverse processes, such as the identity of stem cells in mammalian development to the process of vernalization in plants.

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Conference papers on the topic "Multiprotein complexes"

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Cho, Woo-Cheol, and Ja-Lok Ku. "Abstract 1640: SORBS1-related multiprotein complex regulates metastasis of cancer." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-1640.

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De Sena, Idna Lara Goes. "RELAÇÃO ENTRE O INFLAMASSOMA E A COVID-19 GRAVE." In I Congresso Brasileiro de Imunologia On-line. Revista Multidisciplinar em Saúde, 2021. http://dx.doi.org/10.51161/rems/986.

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INTRODUÇÃO: O inflamassoma é um complexo multiproteico formado no citosol em resposta aos PAMPs e DAMPs. Sua função é gerar as formas ativas das citocinas IL-1β e IL-18 que, antes de serem liberadas das células, são clivadas pela caspase-1, tornando-se ativas para promoverem a resposta inflamatória. A ativação do inflamassoma tem como consequência a piroptose, uma forma inflamatória de morte celular programada de macrófagos caracterizada pelo inchaço das células, perda da integridade da membrana plasmática e liberação de citocinas pró-inflamatórias (IL-1β, IL-18, TNF-α, IL-6 e IL-8). OBJETIVO:

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Leclerc, Guy J., and Julio C. Barredo. "Abstract 4359: Folylpolyglutamate synthetase expression is transcriptionally regulated by chromatin remodeling and recruitment of a multiprotein corepressor complex associated to non-random fusions in ALL." In Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-4359.

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Sand, Jordan M., Emily M. Siebers та Ajit K. Verma. "Abstract 1591: Protein kinase Cε, which is linked to ultraviolet radiation-induced cutaneous damage and development of squamous cell carcinomas, associates with Hsp90β, a core component of multiprotein complex inolving several collaborating chaperones Hsp70/Hsp40, Hop/sti, Cdc37 and p21". У Proceedings: AACR 101st Annual Meeting 2010‐‐ Apr 17‐21, 2010; Washington, DC. American Association for Cancer Research, 2010. http://dx.doi.org/10.1158/1538-7445.am10-1591.

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Reports on the topic "Multiprotein complexes"

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Adams, Michael W., and Michael W. W. Adams. MAGGIE Component 1: Identification and Purification of Native and Recombinant Multiprotein Complexes and Modified Proteins from Pyrococcus furiosus. Office of Scientific and Technical Information (OSTI), 2014. http://dx.doi.org/10.2172/1113776.

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Sessa, Guido, and Gregory Martin. role of FLS3 and BSK830 in pattern-triggered immunity in tomato. United States Department of Agriculture, 2016. http://dx.doi.org/10.32747/2016.7604270.bard.

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Pattern-recognition receptors (PRRs) located on the plant cell surface initiate immune responses by perceiving conserved pathogen molecules known as pathogen-associated molecular patterns (PAMPs). PRRs typically function in multiprotein complexes that include transmembrane and cytoplasmickinases and contribute to the initiation and signaling of pattern-triggered immunity (PTI). An important challenge is to identify molecular components of PRR complexes and downstream signaling pathways, and to understand the molecular mechanisms that mediate their function. In research activities supported by

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Weiss, David, and Neil Olszewski. Manipulation of GA Levels and GA Signal Transduction in Anthers to Generate Male Sterility. United States Department of Agriculture, 2000. http://dx.doi.org/10.32747/2000.7580678.bard.

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The original objectives of the research were: i. To study the role of GA in anther development, ii. To manipulate GA and/or GA signal transduction levels in the anthers in order to generate male sterility. iii. To characterize the GA signal transduction repressor, SPY. Previous studies have suggested that gibberellins (GAs) are required for normal anther development. In this work, we studied the role of GA in the regulation of anther development in petunia. When plants were treated with the GA-biosynthesis inhibitor paclobutrazol, anther development was arrested. Microscopic analysis of these

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