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Keywords: protein engineering
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Biochem J (2024) 481 (24): 2017–2036.
Published: 23 December 2024
..., the electrochemical performance of Geobacter ’s biofilms in MFCs remains challenging to implement industrially. Multiple approaches are being investigated to enhance MFC technologies. Protein engineering of multihaem cytochromes, key components of Geobacter ’s EET pathways, can, conceivably, be pursued to improve...
Includes: Supplementary data
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Biochem J (2023) 480 (16): 1317–1330.
Published: 25 August 2023
... and deubiquitinase activity with the OTUD1 substrate RIPK1 were inhibited. Herein we describe the development of molecular tools for exploring the activity of OTUD1 in a cellular context, towards protein-based therapeutics. deubiquitinases inhibitor phage display protein engineering ubiquitin variants UIM...
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Biochem J (2023) 480 (14): 1097–1107.
Published: 17 July 2023
... a transformative agreement with MALMAD. auto-cleavage auto-degradation enzyme engineering matrix metalloproteases MMP-9 protein engineering Matrix metalloproteinases (MMPs) are a family of proteases, comprising more than twenty different enzymes in humans. They are composed of a catalytic domain...
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Biochem J (2023) 480 (2): 127–140.
Published: 23 January 2023
..., and that strongly depend on the precise goals that each Synthetic Biology project pursues. Protein Engineering is also a very recent area of research, and de novo design of proteins is much increasing our repertoire of nanodevices [ 8 ], instrumental for Synthetic Biology purposes. One of the first attempts...
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Biochem J (2021) 478 (15): 3047–3062.
Published: 13 August 2021
...). Protein was concentrated to 3 mg/ml, flash-cooled in liquid nitrogen and stored at −80°C. © 2021 The Author(s). Published by Portland Press Limited on behalf of the Biochemical Society 2021 acetyltransferases enzyme activation metalloenzymes molecular mechanisms protein engineering...
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Biochem J (2020) 477 (9): 1701–1719.
Published: 11 May 2020
... i , and ∑ # reads mut, i is the sum of all the reads for all mutants in library fraction i . metalloproteases next-generation sequencing protease inhibitor protein engineering protein–protein interactions Protein fitness — the ability of a protein to perform its main function...
Includes: Supplementary data
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Biochem J (2020) 477 (8): 1525–1539.
Published: 29 April 2020
... have previously generated active, phosphorylated Nek7 using genetically encoded phospho-Ser [ 34 ]. Unfortunately, we were unable to generate diffraction-quality crystals using this protein. We, therefore, turned to protein engineering to generate an alternative crystal form through manipulation...
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Biochem J (2020) 477 (8): 1483–1497.
Published: 29 April 2020
... to previous studies from a structural perspective. These clashes would potentially lead to reduced substrate binding affinity of McTadA, consistent with our in vitro deamination activity and binding assays. To rescue the deamination activity of McTadA, we carried out two rounds of protein engineering through...
Includes: Supplementary data
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Biochem J (2019) 476 (23): 3631–3647.
Published: 10 December 2019
... is not possible, since position 76 is close to the catalytic disulfide bridge and the presence of a proline at that position is required for a fully functional active-site conformation [ 12 ]. Pro76 is thus strictly conserved in thioredoxins. molecular evolution protein engineering protein folding...
Includes: Supplementary data
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Biochem J (2019) 476 (2): 275–292.
Published: 25 January 2019
... is the adaptation of Listeria monocytogenes to mouse by improving binding of the listerial invasion protein InlA to the murine variant of its cognate receptor E-cadherin by protein engineering [ 26 ]. LukGH is the most potent leukocidin in in vitro assays and ex vivo models [ 13 , 27 – 29...
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Biochem J (2018) 475 (23): 3887–3901.
Published: 12 December 2018
...). Published by Portland Press Limited on behalf of the Biochemical Society 2018 homoserine malate dehydrogenase protein engineering site-directed mutagenesis synthetic biology A central challenge in the creation of a resource-efficient and sustainable bioeconomy lies in the reduction in our...
Includes: Supplementary data
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Biochem J (2018) 475 (7): 1335–1352.
Published: 16 April 2018
... 2018 directed evolution protease inhibitor protein engineering protein–protein interactions (PPIs) serine proteases Extracellular proteases that are aberrantly expressed in the tumor microenvironment are key contributors to cancer growth, progression and metastasis [ 1 – 3 ] and hence...
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Biochem J (2016) 473 (20): 3611–3620.
Published: 11 October 2016
... to infinite scan rate (in practice to 1/scan rate = 0) should correct the effect of any, presumably small, kinetic distortion on the outcome of the pseudo-two-state fits to the truncated profiles. Such extrapolations are described below. protein engineering protein stability resurrected proteins...
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Biochem J (2016) 473 (11): 1563–1578.
Published: 27 May 2016
... neurodegeneration protein engineering Alzheimer's disease (AD) is the most prevalent form of dementia, with 10% of the human population older than 65 years and 40% older than 85 years affected [ 1 ]. Apart from certain forms of inherited AD [ 2 ], age is the major risk factor associated...
Includes: Supplementary data
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Biochem J (2016) 473 (10): 1329–1341.
Published: 11 May 2016
..., an enzyme that contributes to progression and metastasis of lung, prostate, breast and pancreatic cancers. cancer therapy directed evolution enzyme inhibition mesotrypsin protease inhibitor protein engineering proteolysis X-ray structure Our unique screening strategy, designated ‘triple...
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Biochem J (2011) 435 (2): 345–354.
Published: 29 March 2011
... analysis protein engineering substrate specificity Enzymes are biological catalysts that are essential components of every biological system and are valuable in biotechnology. The key functional characteristics of an enzyme are its catalytic activity towards different substrates and its substrate...
Includes: Supplementary data
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Biochem J (2011) 435 (1): 55–63.
Published: 15 March 2011
...://creativecommons.org/licenses/by-nc/2.5/ ) which permits unrestricted non-commercial use, distribution and reproduction in any medium, provided the original work is properly cited. avidin biotin protein engineering protein–ligand interaction streptavidin traptavidin The capture of the small molecule...
Includes: Supplementary data
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Biochem J (2011) 435 (1): 1–16.
Published: 15 March 2011
... 2010 10 12 2010 © The Authors Journal compilation © 2011 Biochemical Society 2011 procoagulant protease therapy protein degradation protein engineering trypsin fold In an indirect route to protease therapy, stimulation of endogenous protease activity by protein cofactors...
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Biochem J (2008) 414 (2): 205–214.
Published: 12 August 2008
... protein engineering RbcX ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) Rubisco [ribulose-P 2 (D-ribulose-1,5-bisphosphate) carboxylase/oxygenase; EC 4.1.1.39] is the enzyme employed by almost all photoautotrophic organisms to initiate the fixation of CO 2 into biomass via the CBB...
Includes: Supplementary data
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Biochem J (2007) 404 (3): 517–524.
Published: 29 May 2007
... metabolic engineering protein engineering ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) Rubisco (ribulose-1,5-bisphosphate carboxylase/oxygenase) catalyses the nucleophilic carboxylation of ribulose-P 2 ( D -ribulose-1,5-bisphosphate). This conversion of inorganic CO 2...
Includes: Supplementary data
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Biochem J (2006) 397 (2): 305–312.
Published: 28 June 2006
... luciferase imaging Photinus pyralis protein engineering Beetle luciferases catalyse the efficient transfer of chemical energy into light via a two-step process, utilizing ATP-Mg 2+ , firefly luciferin ( D -LH 2 ) and molecular oxygen, yielding oxyluciferin (LO): A wide range of novel...
Includes: Supplementary data
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Biochem J (2006) 394 (1): 85–93.
Published: 27 January 2006
... 2005 21 11 2005 21 11 2005 The Biochemical Society, London 2006 cyclic protein cyclotide haemolytic activity kalata NMR protein engineering Human type A erythrocytes were washed with PBS and centrifuged at 150  g for 30 s in a microcentrifuge several times until...
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Biochem J (2005) 392 (3): 485–491.
Published: 06 December 2005
... chain. In contrast with wild-type avidin, which contains four identical avidin monomers, scAvd enables each one of the four avidin domains to be independently modified by protein engineering. Therefore the scAvd scaffold can be used to construct spatially and stoichiometrically defined pseudotetrameric...
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Biochem J (2004) 382 (3): 885–893.
Published: 07 September 2004
... To whom correspondence should be addressed (email [email protected] ). 24 2 2004 25 5 2004 11 6 2004 15 6 2004 The Biochemical Society, London 2004 Cibacron Blue 3GA glutathione S-transferase herbicide detoxification ligandin protein engineering triazine dye...
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Biochem J (2001) 359 (3): 715–720.
Published: 25 October 2001
... from those of abolishing hydrogen-bond donor potential. This suggests that Trp-59 has both a local and a global stability effect by solvating a buried charge and by having a key role in the packing of the cytochrome c hydrophobic core. Key words: non-coded amino acids, protein engineering, semi...
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Biochem J (2001) 358 (1): 101–110.
Published: 08 August 2001
...2001 2001 essential dynamics herbicide detoxification molecular dynamics protein engineering Abbreviations used: CDNB, 1-chloro-2,4-dinitrobenzene; G-site, GSH binding site; GST, glutathione S-transferase; H-site, electrophile binding site; Ni-NTA, Ni 2+ -nitrilotriacetate. Biochem...
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Biochem J (2001) 354 (2): 455–463.
Published: 22 February 2001
... protein engineering site-directed mutagenesis Biochem. J. (2001) 354, 455 463 (Printed in Great Britain) 455 Active-site characterization of Candida boidinii formate dehydrogenase Nikolaos E. LABROU*1 and Daniel J. RIGDEN‹ *Laboratory of Enzyme Technology, Department of Agricultural Biotechnology...
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Biochem J (2000) 345 (2): 247–254.
Published: 10 January 2000
... of the location of the ligand on the toxin and they were found to release the restrictocin fragment efficiently on proteolysis in Šitro. Key words: chimaeric toxins, protease, protein engineering, targeting, toxins. an intervening specific protease recognition site made them cytotoxic [12,13]. Chimaeric toxins...
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Biochem J (1999) 341 (1): 139–145.
Published: 24 June 1999
...). 4 1 1999 30 3 1999 23 4 1999 The Biochemical Society, London © 1999 1999 acceptor-binding affinity ammodytoxin enzyme activity protein engineering Vipera ammodytes ammodytes Biochem. J. (1999) 341, 139 145 (Printed in Great Britain) 139 An aromatic, but not a basic...
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Biochem J (1999) 339 (2): 309–317.
Published: 08 April 1999
... to denaturants such as guanidine HCl and urea was revealed; the wild-type protein always proved to be the most resistant. The results obtained show the importance of hydrogen bonds and ion pairs in determining protein stability and confirm that simulation methods are able to direct protein engineering in site...