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Keywords: transport
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Biochem J (2024) 481 (19): 1329–1347.
Published: 25 September 2024
...Jonathan Chevriau; Gerardo Zerbetto De Palma; Cintia Jozefkowicz; Victoria Vitali; Agustina Canessa Fortuna; Nicolas Ayub; Gabriela Soto; Gerd Patrick Bienert; Ari Zeida; Karina Alleva Hydrogen peroxide (H 2 O 2 ) transport by aquaporins (AQP) is a critical feature for cellular redox signaling...
Includes: Supplementary data
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Biochem J (2019) 476 (24): 3737–3750.
Published: 17 December 2019
...Sabrina Lusvarghi; Suresh V. Ambudkar P-glycoprotein (P-gp), an ATP-binding cassette transporter associated with multidrug resistance in cancer cells, is capable of effluxing a number of xenobiotics as well as anticancer drugs. The transport of molecules through the transmembrane (TM) region of P...
Includes: Supplementary data
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Biochem J (2019) 476 (1): 25–37.
Published: 07 January 2019
... multifunctional proteins trafficking transport Historically, mitochondria have been perceived almost exclusively as the cell's energy generator, principally responsible for cellular ATP (adenosine triphosphate) production, as well as an evolutionary curiosity due to their endosymbiotic nature and α...
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Biochem J (2017) 474 (11): 1807–1821.
Published: 16 May 2017
...Mohammad Zulkifli; Anand Kumar Bachhawat The proton gradient acts as the driving force for the transport of many metabolites across fungal and plant plasma membranes. Identifying the mechanism of proton relay is critical for understanding the mechanism of transport mediated by these transporters...
Includes: Supplementary data
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Biochem J (2017) 474 (9): 1495–1508.
Published: 19 April 2017
...Sarah M. Smith; Andrew Yarwood; Roland A. Fleck; Colin Robinson; Corinne J. Smith The twin-arginine translocation (Tat) system is an integral membrane protein complex that accomplishes the remarkable feat of transporting large, fully folded polypeptides across the inner membrane of bacteria...
Includes: Supplementary data
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Biochem J (2017) 474 (3): 333–355.
Published: 20 January 2017
... transport system covers a diverse array of proteins involved in metabolic support, neurotransmission and synaptic architecture. Therefore, specific targeting of individual transporter families has the potential to suppress neurodegeneration, a characteristic hallmark of AD. A small number of the 400...
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Biochem J (2016) 473 (21): 3759–3763.
Published: 27 October 2016
...–transporter (‘chansporter’) complexes, which together constitute an emerging theme in cell signaling. Correspondence: Geoffrey W. Abbott ( [email protected] ) neuronal ion transport physiology potassium channels renal ion transport sodium channels transport The primary difference between true...
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Biochem J (2016) 473 (20): 3545–3562.
Published: 11 October 2016
...Mike R. Wilson; Zhanjun Hou; Lucas J. Wilson; Jun Ye; Larry H. Matherly The proton-coupled folate transporter (PCFT; SLC46A1) is a folate–proton symporter expressed in solid tumors and is used for tumor-targeted delivery of cytotoxic antifolates. Topology modeling suggests that the PCFT secondary...
Includes: Supplementary data
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Biochem J (2016) 473 (19): 2911–2935.
Published: 27 September 2016
... functions with an emphasis on mammalian systems. mRNA export nucleocytoplasmic NXF1 RNA processing THO transport Correspondence: Stuart A. Wilson ( [email protected] ) 22 1 2016 11 5 2016 23 5 2016 © 2016 The Author(s) 2016 This is an open access...
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Biochem J (2016) 473 (19): 3237–3252.
Published: 27 September 2016
... cotransporter (NCC) and the epithelial sodium channel (ENaC) are two of the most important determinants of salt balance and thus systemic blood pressure. Abnormalities in either result in profound changes in blood pressure. There is one segment of the nephron where these two sodium transporters are coexpressed...
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Biochem J (2015) 470 (2): 169–179.
Published: 20 August 2015
...Eva S. Schweikhard; Birgitta C. Burckhardt; Friedericke Joos; Cristina Fenollar-Ferrer; Lucy R. Forrest; Stephen A. Kempson; Christine Ziegler The osmolyte and folding chaperone betaine is transported by the renal Na + -coupled GABA (γ-aminobutyric acid) symporter BGT-1 (betaine/GABA transporter 1...
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Biochem J (2013) 454 (3): 371–386.
Published: 29 August 2013
... mitochondrial membrane. Among these carriers, the six-transmembrane-helix mitochondrial SLC25 (solute carrier family 25) proteins facilitate transport of solutes with disparate chemical identities across the inner mitochondrial membrane. Although their proper function replenishes building blocks needed...
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Biochem J (2012) 441 (3): 1007–1016.
Published: 16 January 2012
...Ingrid T. G. W. Bijsmans; Rianne A. M. Bouwmeester; Joachim Geyer; Klaas Nico Faber; Stan F. J. van de Graaf The NTCP (Na + –taurocholate co-transporting protein)/SLC10A [solute carrier family 10 (Na + /bile acid co-transporter family)] 1 is tightly controlled to ensure hepatic bile salt uptake...
Includes: Supplementary data
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Biochem J (2009) 422 (2): 217–228.
Published: 13 August 2009
...Rémy Cailliatte; Bruno Lapeyre; Jean-François Briat; Stéphane Mari; Catherine Curie NRAMP (natural resistance-associated macrophage protein) homologues are evolutionarily conserved bivalent metal transporters. In Arabidopsis , AtNRAMP3 and AtNRAMP4 play a key role in iron nutrition...
Includes: Supplementary data
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Biochem J (2007) 407 (2): 285–292.
Published: 25 September 2007
... The Authors Journal compilation © 2007 Biochemical Society 2007 cell-penetrating peptide cytotoxicity delivery vector penetratin transactivator of transcription (Tat) transport The ability to cross the lipid bilayer of cells and access the cell interior is still one of the major obstacles...
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Biochem J (2007) 401 (2): 365–375.
Published: 21 December 2006
..., especially in higher eukaryotes. Peroxisomes catalyse a number of essential metabolic functions including fatty acid β-oxidation, ether phospholipid biosynthesis, fatty acid α-oxidation and glyoxylate detoxification. The involvement of peroxisomes in these metabolic pathways necessitates the transport...
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Biochem J (2006) 398 (3): 399–409.
Published: 29 August 2006
...Ester Damen; Elmar Krieger; Jens E. Nielsen; Jelle Eygensteyn; Jeroen E. M. Van Leeuwen The retromer complex is involved in the retrograde transport of the CI-M6PR (cation-independent mannose 6-phosphate receptor) from endosomes to the Golgi. It is a hetero-trimeric complex composed of Vps26...
Includes: Supplementary data
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Biochem J (2006) 394 (3): 527–543.
Published: 24 February 2006
... transport through the secretory pathway, gap-junction assembly at the cell surface, internalization and degradation. 1 email [email protected] 5 12 2005 10 1 2006 The Biochemical Society, London 2006 assembly connexin gap junction transport Table 1...
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Biochem J (2005) 389 (3): 717–722.
Published: 26 July 2005
...Wouter F. Visser; Carlo W. van Roermund; Lodewijk Ijlst; Klaas J. Hellingwerf; Ronald J. A. Wanders; Hans R. Waterham It is now well established that the peroxisomal membrane is not freely permeable to small molecules in vivo , which implies the existence of metabolite transporters...
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Biochem J (2005) 388 (3): 745–754.
Published: 07 June 2005
... transporter of the SLC39A family [commonly referred to as the ZIP (Zrt- and Irt-related protein) family] from the gill of zebrafish ( Danio rerio ) ( Dr ZIP1). Dr ZIP1 protein was found to localize at the plasma membrane and to function as a zinc uptake transporter when being expressed in either chinook...
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Biochem J (2004) 381 (3): 905–909.
Published: 27 July 2004
... resistance to current treatments. To study new potential targets, we have functionally characterized two natural variants of the hexose transporter of P. vivax (PvHT) after heterologous expression in Xenopus oocytes. We show that PvHT transports both glucose and fructose. Differences in the affinity...
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Biochem J (2004) 378 (2): 343–351.
Published: 01 March 2004
...Kay BARNES; Jean C. INGRAM; Matthew D. M. BENNETT; Gordon W. STEWART; Stephen A. BALDWIN An acute increase in the V max for glucose uptake occurs in many mammalian cell types after exposure to osmotic or metabolic stress. In the rat epithelial Clone 9 cell line, the glucose transporter isoform...
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Biochem J (2002) 367 (1): 307–312.
Published: 01 October 2002
... transporter system for uptake and its accumulation in cells was prevented by polyamine transport inhibitors. IPENSpm can be classified as a polyamine anti-metabolite and it may be a promising new lead compound in terms of treatment of some human cancers. Biochem. J. (2002) 367, 307 312 (Printed in Great...
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Biochem J (2002) 365 (1): 239–247.
Published: 01 July 2002
... where they, along with their cytosolically generated counterparts possessing a single N -acetylglucosamine residue at their reducing termini (FOSGN1), are trimmed in order to be imported into lysosomes for final degradation. Both the ER and lysosomal FOS transport processes are unable to translocate...
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Biochem J (2001) 360 (3): 589–597.
Published: 10 December 2001
... members of the ATP- binding cassette (ABC) superfamily of membrane transporters are drug-translocating ATPases that pump drugs out of the cytosol, thus conferring drug resistance in both prokaryotes and eukaryotes. This family includes the human multidrug-resistance ( MDR ) P-glycoprotein, which confers...
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Biochem J (2000) 350 (1): 155–162.
Published: 09 August 2000
...-operative ( n = 1.6, [G 1/2 ] = 56mM; where [G 1/2 ] is the glucose concentration at half V max ) because of the glucose-induced activation and recruitment of GLUT2 to the brush-border membrane. Diffusive transport by paracellular flow was negligible. The phloretin-insensitive, SGLT1-mediated, component...
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