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Keywords: protein–protein interaction
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Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2024) 52 (6): 2539–2556.
Published: 13 December 2024
... with JULAC. APP intracellular domain neurodevelopment protein-protein interaction Over the last century, research in Alzheimer's disease (AD) has accumulated a large body of data corroborating the amyloid cascade hypothesis (ACH). ACH posits the extracellular deposition of amyloid-β (Aβ...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2023) 51 (4): 1647–1659.
Published: 30 June 2023
... in mammals. Current knowledge, including genetic analyses of gain- and loss-of-function mutants, highlights the importance of APPs in various physiological functions. Notably, APPs consist of multiple extracellular and intracellular protein-binding regions/domains. Protein–protein interactions are crucial...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2019) 47 (5): 1393–1404.
Published: 24 September 2019
... in zebrafish and mouse. A number of protein–protein interaction partners have been discovered and the potential role of POPDC proteins to control the subcellular localization and function of these interacting proteins will be discussed. Finally, we outline several areas, where research is urgently needed...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2018) 46 (1): 197–206.
Published: 06 February 2018
[email protected] ) 13 9 2017 10 12 2017 8 1 2018 © 2018 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society 2018 co-translational interactions intrinsically disordered proteins multiprotein complexes protein–protein interaction quality control...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2014) 42 (4): 816–821.
Published: 11 August 2014
... on RAF-induced control of MST2 signalling by protein–protein interactions. Finally, we recapitulate some of the direct mechanisms, such as ubiquitin-dependent degradation or gene silencing by promoter hypermethylation, involved in MST2 pathway component down-regulation in cancers. 1...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2014) 42 (2): 395–400.
Published: 20 March 2014
... to determine whether TRICEPS is also suitable for large-scale LRC in plants. cross-linking ligand-based receptor-capture technology protein–protein interaction receptor-like kinase signalling peptide Cell–cell communication events play a key role during developmental processes and reproduction...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2014) 42 (1): 130–138.
Published: 23 January 2014
... cellular development and differentiation [ 3 ], but when deregulated are significant mediators of tumorigenesis in various cancers [ 4 , 5 ]. Ets proteins are subclassified by the presence of further domains associated with PPIs (protein–protein interactions) or transcriptional regulation [ 2 , 3...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2013) 41 (5): 1166–1169.
Published: 23 September 2013
...Oz Sharabi; Jason Shirian; Julia M. Shifman Manipulations of PPIs (protein–protein interactions) are important for many biological applications such as synthetic biology and drug design. Combinatorial methods have been traditionally used for such manipulations, failing, however, to explain...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2013) 41 (5): 1131–1136.
Published: 23 September 2013
...Nicholas Sawyer; Elizabeth B. Speltz; Lynne Regan Protein engineering is at an exciting stage because designed protein–protein interactions are being used in many applications. For instance, three designed proteins are now in clinical trials. Although there have been many successes over the last...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2012) 40 (5): 995–999.
Published: 19 September 2012
... 2012 Calvin cycle CP12 intrinsically disordered protein protein–protein interaction For many years, it had been thought that the ability of a protein to fulfil its cellular function depends on a well-defined three-dimensional structure. In the last decade, however, evidence has...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2012) 40 (4): 624–628.
Published: 20 July 2012
... detection of single protein molecules and protein–protein interactions using synthetic nanopores Anal. Chem. 2008 80 4651 4658 39 Kowalczyk S.W. Hall A.R. Dekker C. Detection of local protein structures along DNA using solid-state nanopores Nano Lett. 2009 10 324 328 40...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2012) 40 (3): 523–530.
Published: 22 May 2012
... equilibrium feedback regulation nucleotide biosynthesis oligomerization protein–protein interaction In all organisms, propagation of genetic material from one generation to the next requires DNA replication. The accuracy of the genetic copy and the repair of mistakes depend on balanced levels...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2012) 40 (1): 124–128.
Published: 19 January 2012
... that functionally compensate for loss of their counterparts in Drosophila . Furthermore, studies in Drosophila and mammalian cell systems showed that Hippo signalling represents a kinase cascade that is tightly regulated by PPIs (protein–protein interactions). Several Hippo signalling molecules contain SARAH...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2011) 39 (5): 1327–1333.
Published: 21 September 2011
...Noha Abdel-Rahman; Alfonso Martinez-Arias; Tom L. Blundell In order to achieve greater selectivity in drug discovery, researchers in both academia and industry are targeting cell regulatory systems. This often involves targeting the protein–protein interactions of regulatory multiprotein assemblies...
Includes: Supplementary data
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2011) 39 (2): 584–588.
Published: 22 March 2011
..., College of Life Sciences, University of Dundee, Dundee DD1 5EH, U.K. 2 9 2010 © The Authors Journal compilation © 2011 Biochemical Society 2011 DNA looping gene therapy protein–protein interaction recognition sequence restriction enzyme Type II restriction endonucleases...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2011) 39 (1): 163–168.
Published: 19 January 2011
... Biochemical Society 2011 archaeon chromosome replication DNA replication protein–protein interaction replication machinery replisome In all forms of cellular life, chromosomal DNA replication requires the complex interplay of a large number of essential and non-essential protein factors...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2010) 38 (6): 1432–1435.
Published: 24 November 2010
... (MLIV) mucolipin protein–protein interaction transient receptor potential mucolipin (TRPML) MLIV (mucolipidosis type IV, MIM#252650) is an LSD (lysosomal storage disorder) presenting unique features in the LSD group either in the clinical picture or the nature of the basic metabolic defect...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2010) 38 (6): 1632–1637.
Published: 24 November 2010
... The Authors Journal compilation © 2010 Biochemical Society 2010 mRNA stability phosphorylation protein–protein interaction translation tristetraprolin (TTP) yeast two-hybrid screen ARE AU-rich element IL interleukin IP immunoprecipitation LPS lipopolysaccharide...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2010) 38 (4): 947–951.
Published: 26 July 2010
...Vadim B. Vasilyev The first detailed report of a specific interaction of CP (caeruloplasmin) with another protein described its complex with LF (lactoferrin) in 2000. Since then, several protein–protein interactions involving CP have been reported, mostly concerning iron-containing proteins. The CP...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2010) 38 (4): 923–927.
Published: 26 July 2010
... protein–protein interaction Proteomic Complex Detection using Sedimentation (ProCoDeS) tandem affinity purification (TAP) From the perspective of method scaling, the generation of specific antibodies required for affinity purification of complexes becomes rapidly unattainable as the number...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2010) 38 (4): 901–907.
Published: 26 July 2010
... large dynamic range (dissociation constants from 10 −12 M to 10 −1 M). In the present paper, we review some of the advances that have been made in the two different types of sedimentation experiment – sedimentation equilibrium and sedimentation velocity – for the analysis of protein–protein interactions...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2010) 38 (4): 940–946.
Published: 26 July 2010
...Parvez I. Haris For most biophysical techniques, characterization of protein–protein interactions is challenging; this is especially true with methods that rely on a physical phenomenon that is common to both of the interacting proteins. Thus, for example, in IR spectroscopy, the carbonyl vibration...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2010) 38 (2): 388–394.
Published: 22 March 2010
..., control protein–protein interactions, which in turn determine whether recombination proceeds. The present review brings together the evidence for this model derived from the studies on φC31 integrase, Bxb1 integrase and other related proteins. 1 To whom correspondence should be addressed (email...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2009) 37 (4): 768–771.
Published: 22 July 2009
... interaction datasets can be used to study functional evolution directly. In terms of constraining change, the co-evolution of interacting molecules is a very subtle process. This has implications for the signal being used to predict protein–protein interactions. In terms of functional change, the ‘rewiring...
Articles
Bostjan Kobe, Gregor Guncar, Rebecca Buchholz, Thomas Huber, Bohumil Maco, Nathan Cowieson, Jennifer L. Martin, Mary Marfori, Jade K. Forwood
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2008) 36 (6): 1438–1441.
Published: 19 November 2008
... structural information on protein–protein complexes, and it yields the most detailed structural information about the interaction. However, there is a major issue when using MX to study protein–protein interactions: a crystal structure does not define a unique protein–protein interface. A crystal...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2008) 36 (6): 1442–1447.
Published: 19 November 2008
... by hydrophobic collapse and helix formation, whereas later events account for the consolidation of more intricate intermolecular electrostatic interactions. activator protein-1 (AP-1) basic leucine zipper (bZIP) interfering peptide protein-fragment complementation assay (PCA) protein–protein interaction...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2008) 36 (6): 1414–1417.
Published: 19 November 2008
...Ishu Saraogi; Andrew D. Hamilton The inhibition of protein–protein interactions using small molecules is a viable approach for the treatment of a range of pathological conditions that result from a malfunctioning of these interactions. Our strategy for the design of such agents involves the mimicry...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2008) 36 (6): 1422–1426.
Published: 19 November 2008
...) 1 Correspondence may be addressed to either of these authors (email [email protected] or [email protected] ). 29 7 2008 © The Authors Journal compilation © 2008 Biochemical Society 2008 fast kinetics iron acquisition protein–protein interaction...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2008) 36 (3): 479–482.
Published: 21 May 2008
... addition to techniques for the investigation of protein–protein interactions in this model organism. 1 To whom correspondence should be addressed (email [email protected] ). 28 1 2008 © The Authors Journal compilation © 2008 Biochemical Society 2008 BiFC bimolecular...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2008) 36 (2): 157–166.
Published: 20 March 2008
... cleavages release NICD in the receiving cell, providing access to the nucleus and complex formation with CSL (see the text for details). ADAM, a disintegrin and metalloproteinase; E(spl) , Enhancer of split . ankyrin repeat intrinsic disorder Notch signalling protein–protein interaction...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2007) 35 (6): 1634–1637.
Published: 23 November 2007
...–protein interaction translation regulation Gene expression can be regulated at numerous levels from alterations in the chromatin state of the gene through to transcription of DNA, processing and translation of the mRNA to post-translational modification of the protein. At the post-transcriptional...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2007) 35 (6): 1389–1392.
Published: 23 November 2007
... histone deacetylase (HDAC) protein–protein interaction small ubiquitin-related modifier (SUMO) transcriptional activation transcriptional repression There is now substantial evidence for the involvement of SUMO modification in the regulation of gene expression [ 1 , 2 ]. From first principles...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2007) 35 (5): 835–847.
Published: 25 October 2007
... protein–protein interaction protein targeting twin-arginine translocase The efficient targeting of proteins to their sites of physiological function is an essential feature of all biological systems. The Tat (twin-arginine transport) system is a protein-targeting pathway found in all kingdoms...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2007) 35 (5): 962–965.
Published: 25 October 2007
... protein synthesis protein in situ array protein–protein interaction protein–ribosome–mRNA complex (PRM complex) proteomic technology ribosome display Here, two cell-free protein technologies, ribosome display and PISA (protein in situ array), are described. Both technologies are discovery...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2007) 35 (5): 1021–1026.
Published: 25 October 2007
... selective competitive inhibitor peptides and allosteric agonist peptides of individual PKC isoenzymes. The strategies and rationale used to identify these peptide regulators of protein–protein interaction may be applicable to other signalling events. Importantly, the PKC-regulating peptides proved...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2007) 35 (5): 966–969.
Published: 25 October 2007
...S. Rotem; C. Katz; A. Friedler ASPP (apoptosis-stimulating protein of p53) 2 is a pro-apoptotic protein that stimulates the p53-mediated apoptotic response. Here, we provide an overview of the structure and protein–protein interactions of ASPP2. The C-terminus of ASPP2 contains Ank (ankyrin...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2007) 35 (5): 970–973.
Published: 25 October 2007
.... The underlying luminal protein–protein interactions, however, are inherently difficult to analyse, mainly due to their transient nature and the rather specialized environment of the ER. To overcome these limitations, we developed a PCA (protein fragment complementation assay) based on the citrine variant of YFP...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2007) 35 (4): 764–766.
Published: 20 July 2007
..., M.B., Lim, E.M.L., Thomas, W.G. and Eidne, K.A. Extended bioluminescence resonance energy transfer (eBRET) for monitoring prolonged protein-protein interactions in live cells, pp. 1664–1670, © 2006, with permission from Elsevier. A number of studies have now utilized BRET to investigate...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2007) 35 (3): 502–507.
Published: 22 May 2007
... in the structure. RhlB is similar, but contains loop extensions (L1). Based on our analysis of the protein–protein interactions between the components of the degradosome, we estimate that its cumulative mass may be in excess of 2.5 MDa [ 28 ]. In many stable complexes in the cell that are made of multiple...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2007) 35 (3): 551–554.
Published: 22 May 2007
... against both wild-type and mutated proteases. They are therefore promising alternatives to active-site-directed inhibitors in AIDS therapy. Disruption of protein–protein interactions by small molecules is a new way to obtain potentially therapeutic molecules. 1 To whom correspondence should...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2006) 34 (6): 1054–1057.
Published: 25 October 2006
... the events of transactivation, the AR makes specific protein–protein interactions with several basal transcription factors such as TBP (TATA-box-binding protein) and TFIIF (transcription factor IIF). These interactions occur predominantly within a defined region termed AF1 (activation function-1) located...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2006) 34 (5): 679–682.
Published: 25 October 2006
.... Until recently, all protein interactions had to be determined in vitro using biochemical approaches: this biochemical legacy has provided cell biologists with the basis to test defined protein–protein interactions not only inside cells, but now also with high spatial resolution. These techniques can...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2006) 34 (5): 971–974.
Published: 25 October 2006
... The Biochemical Society 2006 folded protein guanine nucleotide dissociation inhibitor (GDI) Rho GTPase protein–protein interaction talin vinculin Figure 1 Structure of talin-(1843–1973), showing the four-helix bundle (colouring from blue at the N-terminus to red at the C-terminus) The helix...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2006) 34 (2): 317–319.
Published: 20 March 2006
... mimicry MfpA ocr protein–protein interaction uracil glycosylase The interactions of proteins, and particularly of enzymes, with DNA are tightly controlled spatially and temporally to ensure appropriate treatment of the genome. A classical method of control is the use of sequence-specific DNA...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2006) 34 (1): 162–164.
Published: 20 January 2006
.... 2001 26 369 376 © 2006 The Biochemical Society 2006 Azotobacter vinelandii conformational change NifL–NifA system nitrogen fixation protein–protein interaction redox regulation Expression of nif genes required for nitrogen fixation in Azotobacter vinelandii...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2005) 33 (1): 105–107.
Published: 01 February 2005
... have enabled us to define a chaperone-mediated ‘proofreading’ mechanism involved in co-ordinating assembly and export of twin-arginine transport-dependent enzymes. molecular chaperone [NiFe] hydrogenase protein–protein interaction Tat protein transport system N -oxide reductase twin-arginine...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2004) 32 (6): 1103–1106.
Published: 26 October 2004
... fusion protein. The findings from initial experiments suggest an increase in transcription initiation and elongation rates by AR-AF1–Lex. The role of protein–protein interactions involving co-activators and basal transcription factors and AR-AF1 activity are discussed. 1 To whom correspondence...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2002) 30 (4): 373–378.
Published: 01 August 2002
...M. R. Roberts; G. L. de Bruxelles 14-3-3 proteins regulate a wide range of target proteins via direct protein-protein interactions. The target-binding domain in 14-3-3 proteins is highly conserved, suggesting similar biochemical properties for all 14-3-3s. However, higher eukaryotes possess...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2002) 30 (2): 47–51.
Published: 01 April 2002
..., pyruvate decarboxylase E2p, dihydrolipoyl acetyltransferase E2o, dihydrolipoyl succinyltransferase E3, dihydrolipoyl dehydrogenase PDH, pyruvate dehydrogenase T 2 , transverse relaxation time lipoic acid lipoyl domain protein-protein interaction pyruvate dehydrogenase Metabolite...
Articles
Journal:
Biochemical Society Transactions
Biochem Soc Trans (2000) 28 (6): 615–616.
Published: 01 December 2000
... interacted with ACP in the yeast nucleus. © 2000 Biochemical Society 2000 enoyl-ACP reductase protein-protein interaction yeast two hybrid ACP, acyl carrier protein DES, stearoyl-ACP desaturase ENR enoyl-ACP reductase FAS, fatty acid synthase TE, acyl-ACP thioesterase Fatty Acid...