Results 251 to 260 of about 30,422 (298)
Some of the next articles are maybe not open access.
Vision Research, 1975
Iodoacetamide and its spin-labeled derivative in high concentration ranges (10−2−10−1M) react with unexposed SH-groups of rhodopsin in the dark. The spin-labels bound to these SH-groups are moderately immobilized. While rhodopsin is not spin-labeled with the iodoacetamide at a lower concentration (5 × 10−4 m) in the dark, photobleached rhodopsin is ...
openaire +2 more sources
Iodoacetamide and its spin-labeled derivative in high concentration ranges (10−2−10−1M) react with unexposed SH-groups of rhodopsin in the dark. The spin-labels bound to these SH-groups are moderately immobilized. While rhodopsin is not spin-labeled with the iodoacetamide at a lower concentration (5 × 10−4 m) in the dark, photobleached rhodopsin is ...
openaire +2 more sources
Behavior of spin labels in a variety of interdigitated lipid bilayers [PDF]
Biochimica Et Biophysica Acta - Biomembranes, 1989 The behavior of a number of spin labels in several lipid bilayers, shown by X-ray diffraction to be interdigitated, has been compared in order to evaluate the ability of the spin label technique to detect and diagnose the structure of lipid bilayers. The
Anthony Watts, J M Boggs, G Rangaraj
exaly +2 more sources
Biosynthesis of spin-labeled peptidoglycan: spin-spin interactions
Biochemistry, 1977Membrane preparations from Gaffkya homari catalyzed the in vitro biosynthesis of soluble uncross-linked spin-labeled peptidoglycan, a uniformly labeled polynitroxide, from the spin-labeled nucleotide UDP-MurNAc-Ala-DGlu-Lys(Nepsilon-2,2,5,5-tetramethyl-1-pyrrolin-1-oxyl-3-carbonyl)-DAla-DAla (I) and UDP-GlcNAc.
L S, Johnston, F C, Neuhaus
openaire +2 more sources
Analytical Biochemistry, 1978
Abstract A spin-label assay for lysozyme, which is based on the enzymatic hydrolysis of spin-labeled peptidoglycan, is described. Hydrolysis of this polymer by lysozyme results in sharpening of the esr spectrum. The rate of spectral sharpening is a function of enzyme concentration. When the activities of hen egg-white and human lysozymes are compared
L S, Johnston, F C, Neuhaus
openaire +2 more sources
Abstract A spin-label assay for lysozyme, which is based on the enzymatic hydrolysis of spin-labeled peptidoglycan, is described. Hydrolysis of this polymer by lysozyme results in sharpening of the esr spectrum. The rate of spectral sharpening is a function of enzyme concentration. When the activities of hen egg-white and human lysozymes are compared
L S, Johnston, F C, Neuhaus
openaire +2 more sources
Quarterly Reviews of Biophysics, 1981
The spin label method developed by McConnell 15 years ago is now widely used in studies of the structure and dynamic properties of a variety of the biological systems such as proteins and protein complexes, lipids and membranes, nucleic acids, nucleoproteins, etc.The ESR spectrum of the nitroxide radcal – the spin label – is very sensitive to its ...
S G, Kamzolova, G B, Postnikova
openaire +2 more sources
The spin label method developed by McConnell 15 years ago is now widely used in studies of the structure and dynamic properties of a variety of the biological systems such as proteins and protein complexes, lipids and membranes, nucleic acids, nucleoproteins, etc.The ESR spectrum of the nitroxide radcal – the spin label – is very sensitive to its ...
S G, Kamzolova, G B, Postnikova
openaire +2 more sources
Biochemical and Biophysical Research Communications, 1973
The compound 2,2,6,6-tetramethyl-4-[β-N-ethyleneiminopropionyl] oxypiperidine-I-oxyl is used as a spin-label for RNA. The reaction, effected under rather mild conditions, results in 50–70 nucleotides per spin-label. The temperature dependence of the ESR spectra of spin-labeled RNA is used to estimate temperatures corresponding to the beginning of ...
S, Zavriev +3 more
openaire +2 more sources
The compound 2,2,6,6-tetramethyl-4-[β-N-ethyleneiminopropionyl] oxypiperidine-I-oxyl is used as a spin-label for RNA. The reaction, effected under rather mild conditions, results in 50–70 nucleotides per spin-label. The temperature dependence of the ESR spectra of spin-labeled RNA is used to estimate temperatures corresponding to the beginning of ...
S, Zavriev +3 more
openaire +2 more sources
Electron Spin Resonance: Spin Labels
1981In general biological membranes possess no intrinsic paramagnetism and hence in the unlabeled state do not give rise to an electron spin resonance (ESR) spectrum. The introduction of a stable free radical (“spin label”) thus enables one to use ESR spectroscopy to study specific environments within the membrane.
openaire +2 more sources
Spin-labelled Au nanoparticles
Faraday Discussions, 2004A series of Au nanoparticles functionalised with nitroxide spin labels has been prepared and studied by EPR spectroscopy. Samples with low coverage of the spin label were used to investigate the dynamics of the surface-attached labels at different distances from the Au surface. The rotational correlation times of spin labels vary from 10(-10) s to more
Victor, Chechik +6 more
openaire +2 more sources
Spin Labeling of Potassium Channels
2015Potassium channels are the ion channels most extensively studied by structural techniques. Whereas high-resolution crystal structures have provided key insights into the molecular architecture of these channels, spin labeling studies have helped to unveil the dynamic structural aspects underlying their function.
Dylan, Burdette, Adrian, Gross
openaire +2 more sources
Thrombosis Research, 1976
Abstract Human platelets were labelled with a variety of lipophilic and thiol reagent spin probes. Aggregation was not affected by the lipid probes but was blocked by the covalent protein-directed probes. ESR spectra before and after thrombin treatment indicated that lipid structure of the platelet membrane was not affected to any measurable extent ...
F, Sachs, R D, Feinman
openaire +2 more sources
Abstract Human platelets were labelled with a variety of lipophilic and thiol reagent spin probes. Aggregation was not affected by the lipid probes but was blocked by the covalent protein-directed probes. ESR spectra before and after thrombin treatment indicated that lipid structure of the platelet membrane was not affected to any measurable extent ...
F, Sachs, R D, Feinman
openaire +2 more sources