Anion Transport Proteins
Anion Exchange Protein 1, Erythrocyte
Anions
4-Acetamido-4'-isothiocyanatostilbene-2,2'-disulfonic Acid
Sulfobromophthalein
Erythrocyte Membrane
Organic Anion Transport Polypeptide C
4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid
Biological Transport
Carrier Proteins
Organic Anion Transport Protein 1
Erythrocytes
Membrane Transport Proteins
Fatty Acid Transport Proteins
Biological Transport, Active
Probenecid
Ion Transport
p-Aminohippuric Acid
Organic Anion Transporters
Bicarbonates
Monosaccharide Transport Proteins
Organic Anion Transporters, Sodium-Independent
Antiporters
Hydrogen-Ion Concentration
Cation Transport Proteins
Choroid Plexus
Molecular Sequence Data
Cell Membrane
Membrane Proteins
Sodium
Protein Transport
Axonal Transport
Killifishes
Chloride-Bicarbonate Antiporters
Amino Acid Sequence
Kidney Tubules, Proximal
Phenylglyoxal
Multidrug Resistance-Associated Proteins
Chloride Channels
Ion Exchange
Taurocholic Acid
Symporters
ATP-Binding Cassette Transporters
Fluorescein
Uricosuric Agents
Kidney
Cell Membrane Permeability
Glycophorin
Oxalates
Adenosine Triphosphate
Sulfinpyrazone
Mutation
Cystic Fibrosis Transmembrane Conductance Regulator
Tardigrada
Vesicular Transport Proteins
Models, Biological
Base Sequence
Phenolsulfonphthalein
Binding Sites
Ion Channels
2,4-Dichlorophenoxyacetic Acid
Phosphate-Binding Proteins
Electron Transport
Rabbits
Liver
Protein Binding
Cells, Cultured
Cloning, Molecular
Potassium
Membrane Potentials
Transport Vesicles
Glucose Transport Proteins, Facilitative
Escherichia coli
Protein Conformation
Oocytes
Eosine Yellowish-(YS)
Taurine
Niflumic Acid
Fluorescent Dyes
Temperature
Sodium-Bicarbonate Symporters
Blood Proteins
RNA, Messenger
Amino Acid Transport Systems
Xenopus laevis
Rats, Sprague-Dawley
Glucose
Fluoresceins
Electrophoresis, Polyacrylamide Gel
Epithelium
Organic Cation Transport Proteins
Kidney Cortex
Golgi Apparatus
Nucleotide Transport Proteins
Valinomycin
Chlorine
Estrone
RNA, Complementary
Amiloride
Microscopy, Confocal
Nucleoside Transport Proteins
Succinimides
Epithelial Cells
Voltage-Dependent Anion Channels
Xenopus
Cricetinae
Sequence Homology, Amino Acid
Calcium
Dose-Response Relationship, Drug
Acidosis, Renal Tubular
Transfection
Pyridoxal Phosphate
Sodium-Potassium-Chloride Symporters
Iron
Periplasmic Binding Proteins
Models, Molecular
Rats, Wistar
Diphtheria Toxin
Structure-Activity Relationship
Saccharomyces cerevisiae
Extracellular Space
Voltage-Dependent Anion Channel 1
P-Glycoprotein
Dicarboxylic Acid Transporters
Amino Acids
Superoxides
Furosemide
Rats, Inbred Strains
Equilibrative Nucleoside Transport Proteins
Glutathione
Cyclic AMP
Amino Acid Transport Systems, Basic
Protein Structure, Tertiary
Bile Canaliculi
Substrate Specificity
Fatty Acids
Intracellular Membranes
Cystic Fibrosis
Amino Acid Transport Systems, Neutral
Adenosine Triphosphatases
Aquaporins
Cations
Active Transport, Cell Nucleus
Vesicular Biogenic Amine Transport Proteins
Sodium-Potassium-Exchanging ATPase
GABA Plasma Membrane Transport Proteins
Mesocricetus
Enzyme Inhibitors
Chromatography, High Pressure Liquid
Recombinant Fusion Proteins
Peptide Fragments
Prealbumin
Protons
Canalicular multispecific organic anion transporter/multidrug resistance protein 2 mediates low-affinity transport of reduced glutathione. (1/811)
The canalicular multispecific organic anion transporter (cMOAT), a member of the ATP-binding cassette transporter family, mediates the transport of a broad range of non-bile salt organic anions from liver into bile. cMOAT-deficient Wistar rats (TR-) are mutated in the gene encoding cMOAT, leading to defective hepatobiliary transport of a whole range of substrates, including bilirubin glucuronide. These mutants also have impaired hepatobiliary excretion of GSH and, as a result, the bile flow in these animals is reduced. In the present work we demonstrate a role for cMOAT in the excretion of GSH both in vivo and in vitro. Biliary GSH excretion in rats heterozygous for the cMOAT mutation (TR/tr) was decreased to 63% of controls (TR/TR) (114+/-24 versus 181+/-20 nmol/min per kg body weight). Madin-Darby canine kidney (MDCK) II cells stably expressing the human cMOAT protein displayed >10-fold increase in apical GSH excretion compared with wild-type MDCKII cells (141+/-6.1 pmol/min per mg of protein versus 13.2+/-1.3 pmol/min per mg of protein in wild-type MDCKII cells). Similarly, MDCKII cells expressing the human multidrug resistance protein 1 showed a 4-fold increase in GSH excretion across the basolateral membrane. In several independent cMOAT-transfectants, the level of GSH excretion correlated with the expression level of the protein. Furthermore, we have shown, in cMOAT-transfected cells, that GSH is a low-affinity substrate for the transporter and that its excretion is reduced upon ATP depletion. In membrane vesicles isolated from cMOAT-expressing MDCKII cells, ATP-dependent S-(2,4-dinitrophenyl)glutathione uptake is competitively inhibited by high concentrations of GSH (Ki approximately 20 mM). We concluded that cMOAT mediates low-affinity transport of GSH. However, since hepatocellular GSH concentrations are high (5-10 mM), cMOAT might serve an important physiological function in maintenance of bile flow in addition to hepatic GSH turnover. (+info)Genomic structure of the canalicular multispecific organic anion-transporter gene (MRP2/cMOAT) and mutations in the ATP-binding-cassette region in Dubin-Johnson syndrome. (2/811)
Dubin-Johnson syndrome (DJS) is an autosomal recessive disease characterized by conjugated hyperbilirubinemia. Previous studies of the defects in the human canalicular multispecific organic anion transporter gene (MRP2/cMOAT) in patients with DJS have suggested that the gene defects are responsible for DJS. In this study, we determined the exon/intron structure of the human MRP2/cMOAT gene and further characterized mutations in patients with DJS. The human MRP2/cMOAT gene contains 32 exons, and it has a structure that is highly conserved with that of another ATP-binding-cassette gene, that for a multidrug resistance-associated protein. We then identified three mutations, including two novel ones. All mutations identified to date are in the cytoplasmic domain, which includes the two ATP-binding cassettes and the linker region, or adjacent putative transmembrane domain. Our results confirm that MRP2/cMOAT is the gene responsible for DJS. The finding that mutations are concentrated in the first ATP-binding-cassette domain strongly suggests that a disruption of this region is a critical route to loss of function. (+info)Immunohistochemical localization of multispecific renal organic anion transporter 1 in rat kidney. (3/811)
Renal proximal convoluted tubules have an important role, i.e., to excrete organic anions, including numerous drugs and endogenous substances. Recently, multispecific organic anion transporter 1 (OAT1) was isolated from rat kidney. In this study, the cellular and subcellular localization of OAT1 in rat kidney was investigated. Kidneys from normal rats were perfused and fixed with periodate-lysine-paraformaldehyde solution and were then processed for immunohistochemical analysis using the labeled streptavidin-biotin method, preembedding horseradish peroxidase method, and immunogold method. Light microscopic examination revealed immunostaining for OAT1 in the middle portion of the proximal tubule (S2 segment), but not in the initial portion of the proximal convoluted tubule, next to the glomerulus. Nephron segments other than the S2 segment and the renal vasculature were not stained with antibody to OAT1. Electron-microscopic observation using a preembedding method revealed that OAT1 was exclusively expressed in the basolateral membrane of S2 segments of proximal tubules. The immunogold method showed no labeling for OAT1 in the cytoplasmic vesicles, suggesting that OAT1 may not move together with organic anions into the cells. These results are consistent with previous physiologic data showing that organic anions, including para-aminohippurate, are taken up by the basolateral Na+-independent organic anion/dicarboxylate exchanger and excreted at S2 segments. In conclusion, OAT1 was localized to the basolateral membrane of S2 segments of proximal tubules in rat kidneys. (+info)Immunohistochemical distribution and functional characterization of an organic anion transporting polypeptide 2 (oatp2). (4/811)
The rabbit polyclonal antibody against rat organic anion transporting polypeptide 2 (oatp2) was raised and immunoaffinity-purified. Western blot analysis for oatp2 detected two bands ( 74 and 76 kDa) in rat brain and a single band (76 kDa) in the liver. By immunohistochemical analysis, the oatp2 immunoreactivity was specifically high at the basolateral membrane of rat hepatocytes. Functionally, the oatp2-expressing oocytes were found to transport dehydroepiandrosterone sulfate, delta1 opioid receptor agonist [D-Pen2,D-Pen5]enkephalin, Leuenkephalin, and biotin significantly, as well as the substrates previously reported. These data reveal the exact distribution of the rat oatp2 at the protein level in the liver, and that oatp2 appears to be involved in the multispecificity of the uptaking substrates in the liver and brain. (+info)Polyspecific substrate uptake by the hepatic organic anion transporter Oatp1 in stably transfected CHO cells. (5/811)
The rat liver organic anion transporting polypeptide (Oatp1) has been extensively characterized mainly in the Xenopus laevis expression system as a polyspecific carrier transporting organic anions (bile salts), neutral compounds, and even organic cations. In this study, we extended this characterization using a mammalian expression system and confirm the basolateral hepatic expression of Oatp1 with a new antibody. Besides sulfobromophthalein [Michaelis-Menten constant (Km) of approximately 3 microM], taurocholate (Km of approximately 32 microM), and estradiol- 17beta-glucuronide (Km of approximately 4 microM), substrates previously shown to be transported by Oatp1 in transfected HeLa cells, we determined the kinetic parameters for cholate (Km of approximately 54 microM), glycocholate (Km of approximately 54 microM), estrone-3-sulfate (Km of approximately 11 microM), CRC-220 (Km of approximately 57 microM), ouabain (Km of approximately 3,000 microM), and ochratoxin A (Km of approximately 29 microM) in stably transfected Chinese hamster ovary (CHO) cells. In addition, three new substrates, taurochenodeoxycholate (Km of approximately 7 microM), tauroursodeoxycholate (Km of approximately 13 microM), and dehydroepiandrosterone sulfate (Km of approximately 5 microM), were also investigated. The results establish the polyspecific nature of Oatp1 in a mammalian expression system and definitely identify conjugated dihydroxy bile salts and steroid conjugates as high-affinity endogenous substrates of Oatp1. (+info)Transcriptional regulation of molybdoenzyme synthesis in Escherichia coli in response to molybdenum: ModE-molybdate, a repressor of the modABCD (molybdate transport) operon is a secondary transcriptional activator for the hyc and nar operons. (6/811)
Escherichia coli growing under anaerobic conditions produces several molybdoenzymes, such as formate hydrogenlyase (formate to H2 and CO2; hyc and fdhF genes) and nitrate reductase (narGHJI genes). Synthesis of these molybdoenzymes, even in the presence of the cognate transcriptional activators and effectors, requires molybdate in the medium. Besides the need for molybdopterin cofactor synthesis, molybdate is also required for transcription of the genes encoding these molybdoenzymes. In E. coli, ModE was previously identified as a repressor controlling transcription of the operon encoding molybdate transport components (modABCD). In this work, the ModE protein was also found to be a required component in the activation of hyc-lacZ to an optimum level, but only in the presence of molybdate. Mutant ModE proteins which are molybdate-independent for repression of modA-lacZ also restored hyc-lacZ expression to the wild-type level even in the absence of molybdate. Nitrate-dependent enhancement of transcription of narX-lacZ was completely abolished in a modE mutant. Nitrate-response by narG-lacZ and narK-lacZ was reduced by about 50% in a modE mutant. DNase I footprinting experiments revealed that the ModE protein binds the hyc promoter DNA in the presence of molybdate. ModE-molybdate also protected DNA in the intergenic region between narXL and narK from DNase I hydrolysis. DNA sequences (5' TAYAT 3' and 5' GTTA 3') found in ModE-molybdate-protected modABCD operator DNA were also found in the ModE-molybdate-protected region of hyc promoter DNA (5' GTTA-7 bp-CATAT 3') and narX-narK intergenic region (5' GTTA-7 bp-TACAT 3'). Based on these results, a working model is proposed in which ModE-molybdate serves as a secondary transcriptional activator of both the hyc and narXL operons which are activated primarily by the transcriptional activators, FhlA and NarL, respectively. (+info)A spliced variant of AE1 gene encodes a truncated form of Band 3 in heart: the predominant anion exchanger in ventricular myocytes. (7/811)
The anion exchangers (AE) are encoded by a multigenic family that comprises at least three genes, AE1, AE2 and AE3, and numerous splicoforms. Besides regulating intracellular pH (pHi) via the Cl-/HCO3- exchange, the AEs exert various cellular functions including generation of a senescent antigen, anchorage of the cytoskeleton to the membrane and regulation of metabolism. Most cells express several AE isoforms. Despite the key role of this family of proteins, little is known about the function of specific AE isoforms in any tissue, including the heart. We therefore chose isolated cardiac cells, in which a tight control of pHi is mandatory for the excitation-contraction coupling process, to thoroughly investigate the expression of the AE genes at both the mRNA and protein levels. RT-PCR revealed the presence of AE1, AE2 and AE3 mRNAs in both neonatal and adult rat cardiomyocytes. AE1 is expressed both as the erythroid form (Band 3 or eAE1) and a novel alternate transcript (nAE1), which was more specifically characterized using a PCR mapping strategy. Two variants of AE2 (AE2a and AE2c) were found at the mRNA level. Cardiac as well as brain AE3 mRNAs were expressed in both neonatal and adult rat cardiomyocytes. Several AE protein isoforms were found, including a truncated form of AE1 and two AE3s, but there was no evidence of AE2 protein in adult rat cardiomyocytes. In cardiomyocytes transfected with an AE3 oligodeoxynucleotide antisense, AE3 immunoreactivity was dramatically decreased but the activity of the Cl-/HCO3- exchange was unchanged. In contrast, intracellular microinjection of blocking anti-AE1 antibodies inhibited the AE activity. Altogether, our findings suggest that a specific and novel AE1 splicoform (nAE1) mediates the cardiac Cl-/HCO3- exchange. The multiple gene and protein expression within the same cell type suggest numerous functions for this protein family. (+info)Active lucifer yellow secretion in renal proximal tubule: evidence for organic anion transport system crossover. (8/811)
Recent studies show that organic anion secretion in renal proximal tubule is mediated by distinct sodium-dependent and sodium-independent transport systems. Here we investigated the possibility that organic anions entering the cells on one system can exit into the lumen on a transporter associated with the other system. In isolated rat kidneys perfused with 10 microM lucifer yellow (LY, a fluorescent organic anion) plus 100 micrograms/ml inulin, the LY-to-inulin clearance ratio averaged 1.6 +/- 0.2, indicating net tubular secretion. Probenecid significantly reduced both LY clearance and LY accumulation in kidney tissue. In intact killifish proximal tubules, confocal microscopy was used to measure steady-state LY uptake into cells and secretion into the tubular lumen. Probenecid, p-aminohippurate, and ouabain nearly abolished both uptake and secretion. To this point, the data indicated that LY was handled by the sodium-dependent and ouabain-sensitive organic anion transport system. However, leukotriene C4, an inhibitor of the luminal step for the sodium-independent and ouabain-insensitive organic anion system, reduced luminal secretion of LY by 50%. Leukotriene C4 did not affect cellular accumulation of LY or the transport of fluorescein on the sodium-dependent system. A similar inhibition pattern was found for another fluorescent organic anion, a mercapturic acid derivative of monochlorobimane. Thus, both organic anions entered the cells on the basolateral transporter for the classical, sodium-dependent system, but about half of the transport into the lumen was handled by the luminal carrier for the sodium-independent system, which is most likely the multidrug resistance-associated protein. This is the first demonstration that xenobiotics can enter renal proximal tubule cells on the carrier associated with one organic anion transport system and exit into the tubular lumen on multiple carriers, one of which is associated with a second system. (+info)There are several types of RTA, including:
1. Type 1 RTA: This is caused by a defect in the genes that code for the proteins involved in acid secretion in the renal tubules.
2. Type 2 RTA: This is caused by damage to the renal tubules, such as from exposure to certain drugs or toxins.
3. Type 4 RTA: This is caused by a deficiency of the hormone aldosterone, which helps regulate electrolyte levels in the body.
Symptoms of RTA can include:
* Nausea and vomiting
* Abdominal pain
* Fatigue
* Weakness
* Dehydration
* Increased heart rate
* Decreased urine production
RTA can be diagnosed through blood tests that measure the pH levels in the body, as well as tests that assess kidney function and electrolyte levels. Treatment for RTA typically involves correcting any underlying causes, such as stopping certain medications or addressing electrolyte imbalances. In some cases, medications may be prescribed to help regulate acid levels in the body.
Prevention of RTA includes maintaining proper hydration, avoiding exposure to harmful substances, and managing any underlying medical conditions that may increase the risk of developing RTA. Early detection and treatment can help prevent complications and improve outcomes for individuals with RTA.
Symptoms of cystic fibrosis can vary from person to person, but may include:
* Persistent coughing and wheezing
* Thick, sticky mucus that clogs airways and can lead to respiratory infections
* Difficulty gaining weight or growing at the expected rate
* Intestinal blockages or digestive problems
* Fatty stools
* Nausea and vomiting
* Diarrhea
* Rectal prolapse
* Increased risk of liver disease and respiratory failure
Cystic fibrosis is usually diagnosed in infancy, and treatment typically includes a combination of medications, respiratory therapy, and other supportive care. Management of the disease focuses on controlling symptoms, preventing complications, and improving quality of life. With proper treatment and care, many people with cystic fibrosis can lead long, fulfilling lives.
In summary, cystic fibrosis is a genetic disorder that affects the respiratory, digestive, and reproductive systems, causing thick and sticky mucus to build up in these organs, leading to serious health problems. It can be diagnosed in infancy and managed with a combination of medications, respiratory therapy, and other supportive care.
Band 3 anion transport protein
Anion exchange protein 2
Anion exchange protein 3
Solute carrier family 10 member 4
Solute carrier organic anion transporter family member 1B1
Cotransporter
ABCC5
Bilirubin glucuronide
Organic anion transporter 1
OST Family
Solute carrier organic anion transporter family member 4A1
Elwira Lisowska
Anion exchanger family
Rotor syndrome
Alkalosis
Arsenite-transporting ATPase
PDZK1
SLC22A12
Hyperbilirubinemia in adults
Red blood cell
Organic cation transport protein
Marinobacter algicola
AE1
AE2
Mitochondrial membrane transport protein
SLC26A6
Blumeria graminis
Solute carrier organic anion transporter family member 2B1
Southeast Asian ovalocytosis
Organic anion
Sulfide
Voltage-gated ion channel
Yves De Koninck
Loop diuretic
Hypochlorous acid
Wetland
Cystic fibrosis transmembrane conductance regulator
Solute carrier organic anion transporter family member 1B3
Cholestasis
Bilastine
Glyoxylic acid
KCNK3
ABCC6
Potential applications of graphene
Lipid bilayer
Chloride hydroxyl exchanger
Glycolysis
Redox
Michael J. Welsh (biologist)
Counterion
Harvey Lodish
Chalcogen bond
ARC3 family
Chloride anion exchanger
Hypothiocyanite
CLCN5
JCI -
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Фитнес-клуб "Грация"
TRANSPORTERS14
- Members of the SLC26 family constitute a conserved class of anion transport proteins, which encompasses uncoupled transporters with channel-like properties, coupled exchangers and motor proteins. (bvsalud.org)
- We also measure the chloride and proton fluxes through these transporters using electrical recordings in lipid bilayer membranes as a means to probe the functional behavior of these proteins. (nih.gov)
- My laboratory studies the molecular mechanisms of ion channels and transporters, the proteins that catalyze this transport. (stanford.edu)
- To offset these risks, the evidence of numerous membrane transporters such as P-gp, multidrug resistance-associated proteins (MRPs), visceral anion-transporting polypeptide 2 (OATP2) and the biotic cation transporter OCTN2 is controlled by key xenosensors such as PXR and CAR. (gracefit.ru)
- To address this question, we expressed wildtype and mutant hEAAT3 transporters in Xenopus oocytes and measured substrate transport and anion currents mediated by hEAAT3. (nih.gov)
- It was known from previous work that the nucleotide sugar substrates necessary for the synthesis of the linkage region, UDP-xylose (UDP-Xyl), UDP-galactose (UDP-Gal) and UDP-glucuronic acid (UDP-GlcA) were transported into the Golgi apparatus from the cytosol via protein mediated transporters. (umassmed.edu)
- ABC transporters are a family of membrane transporter proteins that regulate the transport of a wide variety of pharmacological agents, potentially toxic drugs, and xenobiotics, as well as anions. (justia.com)
- ABC transporters are homologous membrane proteins that bind and use cellular adenosine triphosphate (ATP) for their specific activities. (justia.com)
- Some of these transporters were discovered as multidrug resistance proteins (like the MDR1-P glycoprotein, or the multidrug resistance protein, MRP1), defending malignant cancer cells against chemotherapeutic agents. (justia.com)
- In general, Nrf2 did not have a marked effect on uptake transporters, but the mRNAs of organic anion transporting polypeptide 1a1, sodium taurocholate cotransporting polypeptide, and organic anion transporter 2 were decreased with Nrf2 activation. (nih.gov)
- Efflux transporters, such as multidrug resistance-associated proteins, breast cancer resistant protein, as well as ATP-binding cassette g5 and g8 were induced by Nrf2. (nih.gov)
- She studies ATP-binding cassette (ABC) transporters, a diverse group of membrane proteins integral to almost every biological process. (nih.gov)
- By pursuing structural and mechanistic studies of ABC transporters, she hopes to understand how nature utilizes the chemical energy of ATP hydrolysis to perform work - transporting substrates against their chemical gradients. (nih.gov)
- Yet whereas other ABC transporters utilize the chemical energy of ATP hydrolysis to transport substrates against their chemical gradients, CFTR conducts anions down their electrochemical gradient. (nih.gov)
Polypeptide2
- of RSV into cells expressing organic anion transporting polypeptide (Oatp) 1a1, 1a4, and 1b2 was also determined. (aspetjournals.org)
- Once inside, these nascent polypeptide chains are bound by a lumenal ER protein called BiP (Immunoglobulin Binding Protein) or Grp 78 (Glucose Regulated Protein 78). (umassmed.edu)
Organic4
- The "reduced in osteosclerosis" transporter (Roct), which shows decreased expression in the osteosclerosis (oc) mutant mouse, has high homology with rat and human organic anion transporter 3 (OAT3). (elsevier.com)
- Elimination routes of CPT-11 also depend on the presence of drug-transporting proteins, notably P-glycoprotein and canalicular multispecific organic anion transporter, present on the bile canalicular membrane. (aacrjournals.org)
- This gene encodes a member of the organic anion transporter family. (antibodies-online.com)
- This protein may also have a physiologic role as granulocyte/pollen-binding protein (GPBP) involved in the removal of certain organic matter and allergens from serum. (nih.gov)
Exchanger2
- The SLC4A1 gene provides instructions for making a protein known as anion exchanger 1 (AE1). (medlineplus.gov)
- The Na+/H+ antiporter NhaC family protein is a kind of Na+/H+ exchanger from the ion transporter (IT) superfamily, which has mainly been identified in the halophilic bacteria of Bacillus. (bvsalud.org)
Negatively charged4
- This protein transports negatively charged atoms (anions) across cell membranes. (medlineplus.gov)
- Membrane proteins whose primary function is to facilitate the transport of negatively charged molecules (anions) across a biological membrane. (bvsalud.org)
- Negatively charged chloride can cross biological membranes only with the help of membrane-spanning proteins such as Cl - channels, which allow passive diffusion of Cl - along its electrochemical gradient, or transporter proteins that couple the movement of Cl - to that of other ions and can thereby establish electrochemical gradients. (elifesciences.org)
- Trace for the use of trace minerals in the treatment or preven- elements absorbed as negatively charged anions, e.g. tion of diabetes. (who.int)
Physiological4
- Use a combination of biochemical and physiological approaches, we seek to understand the protein elements mediating chloride selectivity as well as those involved in regulating the passage of ions across the membrane. (nih.gov)
- CLC proteins are expressed ubiquitously and perform diverse physiological functions in cardiovascular, neuronal, muscular, and epithelial function. (stanford.edu)
- Mammalian CLC proteins comprise both Cl- channels and Cl-/H+ antiporters that carry out fundamental physiological tasks by transporting Cl- across plasma membrane and intracellular compartments. (ox.ac.uk)
- Its identification will help to understand its physiological roles and the diverse ways by which anion-selective pores can be formed. (elifesciences.org)
Plasma Membrane2
- Here we investigate whether such a reduced activity is due to an impairment of the transport mechanism or an alteration in trafficking to the plasma membrane. (nih.gov)
- ASOR is formed by TMEM206 proteins which display two transmembrane domains (TMs) and are expressed at the plasma membrane. (elifesciences.org)
Membrane-protein2
- The Membrane Transport Biophysics Unit focuses on understanding the physical principles governing membrane-protein function. (nih.gov)
- We use a combination of biophysical methods to investigate membrane-protein structure and dynamics together with electrophysiological analyses to directly measure function. (stanford.edu)
Secretion2
- In mammals, newly synthesized proteins destined for secretion are translocated cotranslationally into the lumen of the Endoplasmic Reticulum (ER). (umassmed.edu)
- In patients with cystic fibrosis, mutations in CFTR endogenously expressed in respiratory epithelia leads to reduced apical anion secretion causing an imbalance in ion and fluid transport. (justia.com)
Specificity1
- Here we show for the Cl-/H+ antiporter CLC-5 that the conserved and extracellularly exposed Lys210 residue is critical to determine the anion specificity for transport activity. (ox.ac.uk)
Hydroxyl1
- Metronidazole, being electron-affinic, can accept an electron from neutral free radical centres to generate a reactive cation that binds to an anion such as hydroxyl (OH-), causing a permanent lesion. (who.int)
Regulates1
- CFTR is expressed in a variety of cells types, including absorptive and secretory epithelia cells, where it regulates anion flux across the membrane, as well as the activity of other ion channels and proteins. (justia.com)
Transporter proteins1
- In order to eventually purify one of these transporter proteins, we wanted to reconstitute their activities. (umassmed.edu)
Selectivity1
- The NO3- over Cl- preference of a plant CLC transporter has been pinpointed to a conserved serine residue located at Scen and it is generally assumed that the other two binding sites of CLCs, Sext and Sin, do not substantially contribute to anion selectivity. (ox.ac.uk)
Bicarbonate2
- In alpha-intercalated cells, the exchange of bicarbonate through the AE1 protein allows acid to be released from the cell into the urine. (medlineplus.gov)
- Transferrins are iron binding transport proteins which can bind two Fe(3+) ions in association with the binding of an anion, usually bicarbonate. (nih.gov)
Reduced by an electron transport1
- Metronidazole is heterocyclic nitro derivative in which the nitro group of metronidazole is reduced by an electron transport protein such as NADPH in an anaerobic micro-organism [6,7,12,13]. (who.int)
Renal3
- The SLC4A1 gene mutations involved in SLC4A1 -associated distal renal tubular acidosis lead to production of altered AE1 proteins that are either stuck inside the cell or trafficked to the wrong side of the cell. (medlineplus.gov)
- In autosomal recessive SLC4A1 -associated distal renal tubular acidosis, both copies of the SLC4A1 gene are mutated, so all of the protein produced from this gene is altered and not trafficked correctly. (medlineplus.gov)
- Studies suggest that with the help of glycophorin A, the altered AE1 protein can often get to the cell membrane in red blood cells, which explains why most people with SLC4A1 -associated distal renal tubular acidosis do not have blood cell abnormalities. (medlineplus.gov)
Transmembrane domains1
- CFTR is composed of approximately 1480 amino acids that encode a protein made up of a tandem repeate of transmembrane domains, each containing six transmembrane helices and a nucleotide binding domain. (justia.com)
Lipids1
- In the case of UDP-xylose it was necessary to prepare the liposomes using endogenous Golgi lipids in order to get transport activity similar to that seen in the intact Golgi vesicles. (umassmed.edu)
Expression6
- We determined whether in vivo transporter-mediated hepatobiliary clearance (CL) and hepatic concentrations of rosuvastatin (RSV) in the rat could be predicted by transport activity in sandwich-cultured rat hepatocytes (SCRHs) and/or transporter-expressing cell lines scaled by differences in transporter protein expression between SCRHs, cell lines, and rat liver. (aspetjournals.org)
- Protein expression of Oatps in SCRHs and Oatp-expressing cells was quantified by liquid chromatography tandem mass spectrometry. (aspetjournals.org)
- into Oatp-expressing cells (active transport) plus passive diffusion CL in SCRHs, scaled by the difference in protein expression in Oatp cells versus SCRH versus rat liver, was within 2-fold of that observed in SCRHs or in vivo. (aspetjournals.org)
- for Oatp protein expression. (aspetjournals.org)
- Here, we examined Roct-mediated transport using a Xenopus laevis oocyte expression system. (elsevier.com)
- Strategies to individualize CPT-11 administration schedules based on patient differences in enzyme or protein expression or by coadministration of specific agents modulating side effects are under way and may ultimately lead to more selective chemotherapeutic use of this agent. (aacrjournals.org)
Gene4
- In the autosomal dominant form of the condition, gene mutations affect only one copy of the SLC4A1 gene, and normal AE1 protein is produced from the other copy. (medlineplus.gov)
- This gene encodes a member of the small ubiquitin-related modifier (SUMO) family of eukaryotic proteins. (nih.gov)
- Polymorphisms in the gene encoding this protein may be associated with fatigue and depression in patients suffering from hyperthyroidism. (antibodies-online.com)
- Description of the protein which includes the UniProt Function and the NCBI Gene Summary. (nih.gov)
Concentrations1
- At saturating extracellular anion concentrations, neutralization of Lys210 is of little impact on the anion preference, suggesting an important role of Lys210 on the association rate of extracellular anions to Sext. (ox.ac.uk)
Hydrogen1
- Membrane proteins that allow the exchange of hydrogen ions for potassium ions across the cellular membrane. (harvard.edu)
CFTR2
- One member of the ABC transporter family commonly associated with disease is the cAMP/ATP-mediated anion channel, CFTR. (justia.com)
- In epithelia cells, normal functioning of CFTR is critical for the maintenance of electrolyte transport throughout the body, including respiratory and digestive tissue. (justia.com)
Antiporter3
- However, little is known about the Na+/H+ antiporter NhaC family of proteins in the extremely halophilic archaea. (bvsalud.org)
- Phylogenetic analysis shows that both NhaC1 and NhaC2 belong to the Na+/H+ antiporter NhaC family of proteins and are significantly distant from the identified NhaC proteins from Bacillus. (bvsalud.org)
- Extracellular determinants of anion discrimination of the Cl-/H+ antiporter protein CLC-5. (ox.ac.uk)
Molecules1
- 2, How antigens are transported and loaded onto MHC-I molecules? (nih.gov)
Cellular1
- Sumoylation may play a role in a wide variety of cellular processes, including nuclear transport, DNA replication and repair, mitosis, transcriptional regulation, and signal transduction. (nih.gov)
Genome2
- Bacterial genome projects continue to reveal that these so-called 'lower' organisms express membrane proteins which are remarkably similar to their physiologically important mammalian cousins. (nih.gov)
- We now used a genome-wide siRNA screen to molecularly identify the widely expressed acid-sensitive outwardly-rectifying anion channel PAORAC/ASOR. (elifesciences.org)
19981
- 1998. Ammonia: Emission, atmospheric transport and deposition. (cdc.gov)
Family3
- Our major model proteins are members of the ClC family of anion-transport proteins. (nih.gov)
- A major research focus is on the chloride-selective CLC family, which contains both types ion-transport protein. (stanford.edu)
- WCPs are a family of membrane proteins, belonging to the Membrane Intrinsic Proteins superfamily. (acta-endo.ro)
Vitro2
- We demonstrated that 2,4-D is consistently transported into saliva using both in vitro and in vivo models, making 2,4-D a potential candidate for human non-invasive salivary biomonitoring. (cdc.gov)
- We studied the transport of ATP in vitro and found that ATP enters the lumen of the ER in a saturable manner with a Kmapp~3μM. (umassmed.edu)
Cytosol2
- Since ATP is synthesized mainly in the mitochondria, we hypothesized that there must be an ATP transporter in the ER which would allow the protein mediated transport of ATP from the cytosol into the ER lumen. (umassmed.edu)
- Kelch-like ECH associating protein 1 (Keap1) sequesters Nrf2 in the cytosol. (nih.gov)
Affinity1
- This protein has particularly high affinity for the thyroid hormones thyroxine, tri-iodothyronine and reverse tri-iodothyronine. (antibodies-online.com)
Gradients1
- Such transport sets up and exploits ion gradients, thus providing the basic energy and signaling events that are the foundation of life. (stanford.edu)
Uptake1
- The encoded protein is a transmembrane receptor that mediates the sodium-independent uptake of thyroid hormones in brain tissues. (antibodies-online.com)
Decrease2
- Preliminary data suggest that this reduction in transport activity may arise from a decrease in the efficiency of trafficking of mutant carriers to the cell surface. (nih.gov)
- The resulting decrease in anion transport contributes to enhanced mucus accumulation in the lung and the accompanying microbial infections that ultimately cause death in CF patients. (justia.com)
Structural3
- In addition to exchanging ions, the longer AE1 protein attaches to other proteins that make up the structural framework (the cytoskeleton) of red blood cells, helping to maintain their structure. (medlineplus.gov)
- His laboratory is using a combination of structural and functional approaches to answer mechanistic questions regarding ClC channels and other anion transport proteins. (nih.gov)
- Furthermore, compared to their 'higher' counterparts, these bacterial proteins are often more chemically stable and are easier to purify in large quantities, rendering them amenable to structural analysis. (nih.gov)
Consistently1
- We consistently observe a 50% reduction of the transport activity of the T164A hEAAT3. (nih.gov)
Function2
- We have expressed several such proteins, and are pursuing more detailed analysis of their function and architecture. (nih.gov)
- The function of this protein is to transport iron from the intestine, reticuloendothelial system, and liver parenchymal cells to all proliferating cells in the body. (nih.gov)
Tasks1
- Receptor activator of NF-B ligand (RANKL)-induced osteoclastogenesis is accompanied by intracellular Ca2+ mobilization in a kind of oscillations, which takes on necessary tasks by activating Ca2+/calmodulin-dependent proteins kinase sequentially, nFATc1 and calcineurin, required in the osteoclast differentiation. (bioinf.org)
Ammonia2
- Furthermore, mutant nematodes possessed significantly reduced rates of cytochrome C oxidase activity and ammonia excretion rates, indicating the knockout of NHX-3 induced fundamental changes in metabolism that could impact the nematode's need to eliminate metabolic end-products like H+ and ammonia that relate to NHX transport. (bvsalud.org)
- 1987. A long-range transport model for ammonia and ammonium for Europe. (cdc.gov)
Additionally1
- We additionally apply our expertise on ion-transport mechanisms to interdisciplinary collaborations to create novel chemical tools, to develop CLC-targeted therapies, and to understand the mechanism by which ultrasound modulates ion-transport to effect neuromodulation. (stanford.edu)
Oxidative1
- H2O2-induced oxidative stress affects SO4= transport in human erythrocytes. (unime.it)
Mechanism1
- Currently, we are using fluorescence-based methods to determine the nature and magnitude of conformational changes involved in the transport mechanism of ClC-ec1. (nih.gov)
Explore1
- Recent developments, including the determination of a high-resolution structure of a bacterial ClC, have allowed us to focus our attention on particular regions of these proteins, which we explore with combinations of biochemistry, genetic mutation, and electrical recordings. (nih.gov)
Activity2
- Heterologously expressed proteins bearing this mutation showed a reduced transport activity. (nih.gov)
- Because of this, they represent important potential drug targets for the treatment of diseases associated with defects in the transporter, prevention of drug transport out of the target cell, and intervention in other diseases in which modulation of ABC transporter activity may be beneficial. (justia.com)
Animals1
- Chloride is by far the most abundant anion in animals. (elifesciences.org)
DIDS1
- ATP transport is dependent on time, protein, and vesicle integrity, it is also inhibited by the general anion transport inhibitor, 4,4' diisothiocyano-2,2'-disulfonic acid stilbene (DIDS). (umassmed.edu)
Cells3
- In red blood cells, the AE1 protein can interact with another protein called glycophorin A, which helps ensure AE1 gets moved (trafficked) to the correct location of the cell. (medlineplus.gov)
- The mutations involved in hereditary spherocytosis lead to a reduction of AE1 protein, which results in abnormal red blood cells that are round and spherical rather than a flattened disk shape and are more fragile than usual. (medlineplus.gov)
- Ion transport across the hydrophobic barrier of the cell membrane is a primary challenge faced by all cells. (stanford.edu)
Molecular1
- Elucidation of these roles has been greatly facilitated by the molecular identification of the underlying channel proteins, a discovery process that began in the late 1980's and is still ongoing. (elifesciences.org)