Related ArticlesTransduction of reducing power across the plasma membrane by reduced glutathione. A 1H-NMR spin-echo study of intact human erythrocytes.
Eur J Biochem. 1993 Aug 1;215(3):711-8
Authors: Ciriolo MR, Paci M, Sette M, De Martino A, Bozzi A, Rotilio G
The NMR signal of reduced glutathione (GSH) was monitored in intact human erythrocytes by the 1H spin-echo Carr-Purcell-Meiboom-Gill pulse sequence. Addition of GSH, which was unable to cross the erythrocyte membrane, produced an approximate twofold increase of the GSH signal in glucose-depleted cells. Addition of oxidised glutathione (GSSG), did not affect the signal, and addition of GSH to hemolysates gave a much smaller increase. Reduction of internal GSSG by NADPH-dependent enzymes was excluded by experiments with glucose-supplied or glucose-6-phosphate dehydrogenase deficient cells. Involvement of external thiol groups of the erythrocyte membrane was shown by the lack of effect in cells treated with an impermeable thiol-blocking compound. Involvement of spectrin was indicated by the proportional loss of the effect in erythrocytes with variable genetic deficiency of spectrin. Protein-glutathione mixed disulfides appeared to be the source of the NMR response since an increase of their content, by diamide treatment or aging procedures, produced a higher GSH signal, while their reduction by permeable reductants gave the opposite effect. It is concluded that GSH can transduce its reducing power by a thiol/disulfide exchange mechanism that sequentially involves sulfur-rich proteins spanning across the erythrocyte membrane.
Using NMR metabolomics to investigate tricarboxylic acid cycle-dependent signal transduction in Staphylococcus epidermidis.
Using NMR metabolomics to investigate tricarboxylic acid cycle-dependent signal transduction in Staphylococcus epidermidis.
Using NMR metabolomics to investigate tricarboxylic acid cycle-dependent signal transduction in Staphylococcus epidermidis.
J Biol Chem. 2010 Nov 19;285(47):36616-24
Authors: Sadykov MR, Zhang B, Halouska S, Nelson JL, Kreimer LW, Zhu Y, Powers R, Somerville GA
Staphylococcus epidermidis is a skin-resident bacterium and a major cause of biomaterial-associated infections. The transition from residing on the skin to residing on...
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03-01-2011 12:14 PM
A View into the Blind Spot: Solution NMR Provides New Insights into Signal Transduction Across the Lipid Bilayer.
A View into the Blind Spot: Solution NMR Provides New Insights into Signal Transduction Across the Lipid Bilayer.
Related Articles A View into the Blind Spot: Solution NMR Provides New Insights into Signal Transduction Across the Lipid Bilayer.
Structure. 2010 Dec 8;18(12):1559-1569
Authors: Call ME, Chou JJ
One of the most fundamental problems in cell biology concerns how cells communicate with their surroundings through surface receptors. The last few decades have seen major advances in understanding the mechanisms of receptor-ligand...
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12-08-2010 06:21 PM
[NMR paper] Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected
Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR.
Related Articles Futile cycling of lactate through the plasma membrane of C6 glioma cells as detected by (13C, 2H) NMR.
J Neurosci Res. 2005 Jan 1-15;79(1-2):119-27
Authors: Rodrigues TB, Gray HL, Benito M, Garrido S, Sierra A, Geraldes CF, Ballesteros P, Cerdán S
We report a novel ((13)C, (2)H) nuclear magnetic resonance (NMR) procedure to investigate lactate recycling through the monocarboxylate transporter of the plasma membrane of cells...
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11-24-2010 11:14 PM
[NMR paper] PMP1 18-38, a yeast plasma membrane protein fragment, binds phosphatidylserine from b
PMP1 18-38, a yeast plasma membrane protein fragment, binds phosphatidylserine from bilayer mixtures with phosphatidylcholine: a (2)H-NMR study.
Related Articles PMP1 18-38, a yeast plasma membrane protein fragment, binds phosphatidylserine from bilayer mixtures with phosphatidylcholine: a (2)H-NMR study.
Biophys J. 2000 Nov;79(5):2624-31
Authors: Roux M, Beswick V, Coďc YM, Huynh-Dinh T, Sanson A, Neumann JM
PMP1 is a 38-residue plasma membrane protein of the yeast Saccharomyces cerevisiae that regulates the activity of the H(+)-ATPase. The...
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11-19-2010 08:29 PM
Structure of key protein for cellular signal transduction elucidated - News-Medical.n
Structure of key protein for cellular signal transduction elucidated - News-Medical.net
<img alt="" height="1" width="1" />
Structure of key protein for cellular signal transduction elucidated
News-Medical.net
Using NMR spectroscopy, Professor Michael Sattler and his team elucidated the spatial structure of the Qua1 region of Sam68, which is responsible for the ...
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09-10-2010 12:58 PM
[NMR paper] Reaction of cis- and trans-[PtCl2(NH3)2] with reduced glutathione inside human red bl
Reaction of cis- and trans- with reduced glutathione inside human red blood cells, studied by 1H and 15N- DEPT NMR.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--linkinghub.elsevier.com-ihub-images-PubMedLink.gif Related Articles Reaction of cis- and trans- with reduced glutathione inside human red blood cells, studied by 1H and 15N- DEPT NMR.
J Inorg Biochem. 1990 Apr;38(4):327-45
Authors: Berners-Price SJ, Kuchel PW
Reactions of cis- and trans- with glutathione (GSH) inside intact red blood cells have been studied by 1H spin-echo...
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08-21-2010 10:48 PM
[Nature network NMR forum] NMR in plasma (6 replies)
NMR in plasma (6 replies)
In a previous post on this forum I mentioned that there were some neat methods for doing in-cell nmr.
I have been wondering since then whether any of you had tried just adding stable-isotope-labeled proteins to plasma. Would the results of such an experiment be interesting?
If you know of a paper that describes the results of this, would you please let me know – my PubMed searches have not been fruitful so far.
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08-21-2010 03:29 PM
Reducing the Tedium of NMR Structure Confirmation
The following message was posted by ABowes on old Postnuke of Bionmr.com:
<P class=MsoNormal >Recently, Advanced Chemistry Development, Inc. (ACD/Labs) conducted a comprehensive study of their NMR prediction software using a broad test database consisting of more than 120,000 <SUP>1</SUP>H and <SUP>13</SUP>C NMR chemical shifts. The study reveals that the prediction accuracy of the latest versions (v8.0) has been improved by 45% for the <SUP>13</SUP>C, and 40% for the <SUP>1</SUP>H NMR chemical shifts, maintaining the leading position among NMR prediction software.
ACD/Labs NMR...