1-50 of 66
Keywords: proteolysis
Close
Follow your search
Access your saved searches in your account

Would you like to receive an alert when new items match your search?
Close Modal
Sort by
Articles
Biochem J (2024) 481 (13): 865–881.
Published: 03 July 2024
... (CC BY) . filamin A phosphorylation post translational modification proteolysis The filamins are a group of actin binding, scaffold proteins consisting of three isoforms, Filamin A, B and C. Filamin A (previously termed actin binding protein-280, ABP-280) was the first isoform...
Articles
Biochem J (2024) 481 (1): 33–44.
Published: 04 January 2024
...). Published by Portland Press Limited on behalf of the Biochemical Society 2024 advanced glycation end products diabetes glycation insulin proteolysis solid-phase peptide synthesis The modification of amino acids by hexoses and dicarbonyls can result in the formation of protein-bound...
Includes: Supplementary data
Articles
Biochem J (2023) 480 (22): 1817–1831.
Published: 17 November 2023
... to this work. 31 8 2023 19 10 2023 23 10 2023 © 2023 The Author(s) 2023 This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) . proteolysis ubiquitin...
Includes: Supplementary data
Articles
Biochem J (2022) 479 (22): 2365–2377.
Published: 23 November 2022
... degradation assays showed that HvPSY34 was more stable than HvPSYwt. Collectively, these results show that the C-terminal region of HvPSY contains a ‘recognition determinant’ for proteolysis in H. volcanii . Preliminary evidence suggests that LonB is involved in the recognition mechanism. This study provides...
Includes: Supplementary data
Articles
Biochem J (2017) 474 (9): 1509–1528.
Published: 19 April 2017
... possible interactions were screened with and without co-expression of Lyn tyrosine kinase, respectively. adaptor proteins protein–protein interactions proteolysis transcription factors The Dok (downstream of kinase) family of adapter proteins consists of seven related proteins characterized...
Includes: Supplementary data
Articles
Biochem J (2016) 473 (10): 1329–1341.
Published: 11 May 2016
... and identifies a promising mesotrypsin inhibitor as a starting point for the development of anticancer protein therapeutics. cancer therapy directed evolution enzyme inhibition mesotrypsin protease inhibitor protein engineering proteolysis X-ray structure The human serine protease...
Includes: Supplementary data
Articles
Biochem J (2014) 464 (3): 461–472.
Published: 05 December 2014
... and domain 2 of the norovirus NS6 protease influences cleavage at specific non-structural substrate boundaries. murine norovirus (MNV) norovirus protease polyprotein positive sense proteolysis Noroviruses are members of the calicivirus family of positive-sense, single-stranded RNA viruses...
Includes: Supplementary data
Articles
Articles
Articles
Biochem J (2013) 449 (2): 497–506.
Published: 14 December 2012
... (MAPK) proteolysis Equilibrium between anabolic and catabolic processes preserves the homoeostasis necessary to ensure normal cell growth and development. Upon nutrient deprivation or cellular stress, catabolic processes prevail in order to supply the energy required to maintain cell...
Includes: Supplementary data
Articles
Biochem J (2012) 447 (3): 335–351.
Published: 05 October 2012
... © The Authors Journal compilation © 2012 Biochemical Society 2012 calcium-binding domain structure enzyme activation inhibitor complex proteinase proteolysis X-ray crystallography The present review will focus on insights about calpains and their functioning that have...
Includes: Multimedia, Supplementary data
Articles
Biochem J (2012) 446 (2): 213–223.
Published: 14 August 2012
...André Struglics; Maria Hansson Although it has been shown that aggrecanases are involved in aggrecan degradation, the role of MMP (matrix metalloproteinase) aggrecanolysis is less well studied. To investigate MMP proteolysis of human aggrecan, in the present study we used neoepitope antibodies...
Includes: Supplementary data
Articles
Biochem J (2012) 446 (2): 311–320.
Published: 14 August 2012
... were analysed by PAGE on 12% BisTris gels using the NuPAGE gel system (Invitrogen). Proteins were stained using the colloidal Coomassie Blue method. chloroplast Clp protein cyanobacterium proteolysis Proteolysis performs a vital homoeostatic role in all organisms, within which energy...
Includes: Supplementary data
Articles
Articles
Biochem J (2011) 437 (2): 313–322.
Published: 28 June 2011
...), resulting in a heterodimeric receptor. Upon ligand binding at the cell surface, Notch receptors undergo two successive proteolytic cleavages: an ectodomain cleavage (S2), followed by intramembrane proteolysis by γ-secretase (S3; Figure 1 A) [ 5 ]. This process releases the NICD (Notch intracellular domain...
Includes: Supplementary data
Articles
Biochem J (2011) 435 (2): 391–399.
Published: 29 March 2011
...+ (having higher affinity for CASQ2 than Ca 2+ ) was used to achieve molecular compaction at 0.2 mM, then Ca 2+ was added and turbidity was measured as described above. All turbidity measurements were repeated at least three times. Purified WT and mutants of CASQ2 were subjected to proteolysis...
Includes: Supplementary data
Articles
Biochem J (2010) 430 (3): 531–538.
Published: 27 August 2010
... protease, has a specific role in the proteolysis of aggrecan we developed neoepitope antibodies (anti-PGVA, anti-GDLS and anti-EDLS) against calpain cleavage sites and used Western blot analysis to identify calpain-generated fragments in normal and OA (osteoarthritis) knee cartilage and SF (synovial fluid...
Includes: Supplementary data
Articles
Articles
Biochem J (2009) 421 (3): 397–404.
Published: 15 July 2009
... that requires bound ATP to maintain its component subcomplexes, the 20S proteasome and PA700, in a functionally assembled state. Proteolysis of both types of substrate requires PA700-induced opening of reversible gates at substrate-access pores of the 20S proteasome. In the present study we demonstrate...
Articles
Biochem J (2009) 419 (2): 467–474.
Published: 27 March 2009
... neurite outgrowth neuropeptide Y (NPY) phosphonate inhibitor proteolysis substrate specificity transthyretin In the present study, we investigated the substrate specificity of TTR and assessed whether some of the phenotypes described in TTR-KO mice, namely TTR involvement in PAM expression...
Articles
Articles
Biochem J (2008) 414 (1): 133–141.
Published: 29 July 2008
... Vcx1p's topology using three biochemical assays: C-terminal reporter localization, glycosylation mapping and proteolysis. We have found that the protein has an odd number of TM (transmembrane) domains and that its termini are located on opposite sides of the membrane, with the N-terminus in the cytoplasm...
Includes: Supplementary data
Articles
Articles
Articles
Biochem J (2008) 410 (1): 157–165.
Published: 29 January 2008
..., (ii) the cathelicidin-derived antimicrobial peptide, LL-37, and (iii) the serpin-type plasma protease inhibitors α 1 -antichymotrypsin and α 1 -proteinase inhibitor, thereby potentially promoting bacterial escape from the host immune system, as well as uncontrolled proteolysis, leading to host tissue...
Articles
Biochem J (2007) 408 (3): 429–439.
Published: 28 November 2007
...-Domain are sensitive to proteolysis at the same site. NMR results suggest that the isolated 73aa-Domain is not structured. Iron-independent cleavage of IRP2 within the 73aa-Domain also occurs in lung cancer (H1299) cells. Haem interacts with a cysteine residue only in truncated forms of the 73aa-Domain...
Includes: Supplementary data
Articles
Biochem J (2007) 407 (2): 153–159.
Published: 25 September 2007
...) proteinase proteolysis urinary-type plasminogen activator (uPA) uPA receptor (uPAR) OSCC (oral squamous cell carcinoma), including tumours affecting the tongue, floor of the mouth, buccal mucosa, lips, palate and gingiva, is the most common malignancy of the oral cavity, causing more deaths than...
Articles
Biochem J (2007) 407 (1): e1.
Published: 12 September 2007
... that this methodology provides a comprehensive map of constitutive trimming events mediated by regulatory proteases such as methionine aminopeptidase. This study also identifies previously uncharacterized processing events that highlight potential novel regulatory mechanisms mediated by proteolysis. mass...
Articles
Biochem J (2007) 404 (1): e1.
Published: 26 April 2007
.... A. Chong H. J. Ryan J. J. Mast cell-restricted p70 Stat6 isoform is a product of selective proteolysis Cytokine 2002 19 218 227 22 Piazza F. Valens J. Lagasse E. Schindler C. Myeloid differentiation of FdCP1 cells is dependent on Stat5 processing Blood 2000 96...
Articles
Biochem J (2007) 401 (2): 475–483.
Published: 21 December 2006
...Alana M. Thackray; Lee Hopkins; Raymond Bujdoso PrPSc [abnormal disease-specific conformation of PrP (prion-related protein)] accumulates in prion-affected individuals in the form of amorphous aggregates. Limited proteolysis of PrPSc results in a protease-resistant core of PrPSc of molecular mass...
Articles
Biochem J (2006) 396 (2): e9.
Published: 15 May 2006
...–viral interaction poly(A)-binding protein (PABP) proteolysis Translational control of mRNAs is central to the regulation of gene expression and is important in the aetiology of human disease. Many viruses have evolved complex mechanisms to inhibit host cellular mRNA translation while facilitating...
Articles
Biochem J (2006) 395 (1): 1–19.
Published: 15 March 2006
... to two excellent reviews [ 22 , 23 ]. For a short review on some of the properties of IGFBP-5, see [ 24 ]. extracellular matrix (ECM) glycosaminoglycan insulin-like growth factor-I (IGF-I) insulin-like growth factor-binding protein 5 (IGFBP-5) mammary gland proteolysis The IGF (insulin...
Articles
Biochem J (2006) 394 (1): 355–363.
Published: 27 January 2006
... proteasome in a ubiquitin-independent manner. Such degradation is directed by the disordered N-terminal region of the TS polypeptide, and is abrogated by ligand binding. In the present study, we have verified the ubiquitin-independent nature of TS proteolysis by showing that a ‘lysine-less’ polypeptide...
Articles
Biochem J (2006) 393 (1): 59–67.
Published: 12 December 2005
... endocytosis gap junction PMA proteolysis Neighbouring cells are able to exchange ions, metabolites and cell-signalling molecules of <1 kDa via hydrophilic channels composed of proteins called connexins [ 1 ]. Connexins are tetramembrane-spanning proteins that oligomerize into hemichannels [ 2...
Articles
Biochem J (2005) 392 (3): 443–448.
Published: 06 December 2005
... structure. Oxidation is attenuated when both binding sites are occupied by CBHcy, but Met alone has no effect. Partial digestion of ligand-free BHMT with trypsin produces two large peptides, excising a seven-residue peptide within loop L2. CBHcy but not Met binding slows down proteolysis by trypsin...
Articles
Articles
Biochem J (2005) 388 (1): 81–91.
Published: 10 May 2005
... active tetrameric form of human CPN in plasma. Although it is known that CPN is sensitive to cleavage by plasmin and other serine proteases [ 16 , 27 ], the cleavage sites in CPN have never been identified and the effects of proteolysis on the activity and quaternary structure of CPN have not been...
Articles
Biochem J (2005) 387 (3): 659–667.
Published: 26 April 2005
... cell leukaemia-1 (Mcl-1) nuclear localization proteolysis The Bcl-2 family of proteins are known regulators of cell death and survival, acting as regulators of membrane integrity at both the mitochondria and the endoplasmic reticulum [ 1 – 5 ]. They are characterized by the presence of one...
Articles
Biochem J (2005) 387 (2): 497–506.
Published: 05 April 2005
..., London 2005 ectodomain matrix metalloproteinase (MMP) shedding protease proteolysis tissue inhibitor of metalloproteinase (TIMP) MT1-MMP (membrane type 1 matrix metalloproteinase) is a type I membrane-anchored MMP that has been shown to play a critical role in the pericellular...
Includes: Supplementary data
Articles
Articles
Biochem J (2003) 376 (3): 577–586.
Published: 15 December 2003
...Amina TASSA; Marie Paule ROUX; Didier ATTAIX; Daniel M. BECHET Increased proteolysis contributes to muscle atrophy that prevails in many diseases. Elucidating the signalling pathways responsible for this activation is of obvious clinical importance. Autophagy is a ubiquitous degradation process...
Articles
Biochem J (2003) 375 (1): 191–197.
Published: 01 October 2003
... in intact, healthy tissues suggests that this MMP functions in physiological tissue homoeostasis and turnover. Key words: alternative splicing, extracellular matrix, matrix metalloproteinase, proteolysis, tissue expression. INTRODUCTION The matrix metalloproteinases (MMPs) comprise a family of at least 21...
Articles
Articles
Articles
Biochem J (2003) 370 (3): 1047–1054.
Published: 15 March 2003
..., prenylation, proteolysis, Ras. cleaves the precursor of the yeast a-factor mating pheromone after the farnesylated cysteine residue and also at a second point close to the N-terminus of the precursor peptide [3 7]. The second gene encodes Rce1p, a protein that seems to be directly involved in the C-terminal...
Articles
Biochem J (2003) 370 (1): 265–273.
Published: 15 February 2003
.... Given the facts that cell-cycle-dependent proteolysis is highly conserved in all eukaryotes and yeast cells are an excellent model system for protein-degradation study, here we report on the use of Saccharomyces cerevisiae and Schizosaccharomyces pombe to investigate the degradation signal and mechanism...
Articles
Articles
Articles
Biochem J (2002) 367 (1): 209–217.
Published: 01 October 2002
...Roman ZWICKY; Kathrin MÜNTENER; Mary B. GOLDRING; Antonio BAICI Cathepsin B, a marker of the dedifferentiated chondrocyte phenotype, contributes to cartilage destruction in osteoarthritis and pathological proteolysis in rheumatoid arthritis and cancer. In search of possible means for neutralizing...
Articles