Search Results - "Bashford, C L"
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Specialized scanning ion‐conductance microscope for imaging of living cells
Published in Journal of microscopy (Oxford) (01-10-1997)“…A specialized scanning ion conductance microscope (SICM) for imaging living cells has been developed from a conventional patch‐clamp apparatus, which uses a…”
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2
Conductance Studies on Trichotoxin_A50E and Implications for Channel Structure
Published in Biophysical journal (01-09-2004)“…Trichotoxin_A50E is an 18-residue peptaibol whose crystal structure has recently been determined. In this study, the conductance properties of trichotoxin_A50E…”
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3
Understanding the tumor metabolic phenotype in the genomic era
Published in Current molecular medicine (01-02-2003)“…Now, at the beginning of a new century, 80 years after Warburg's Nobel prize winning discoveries, we are beginning to make sense of the underlying causes of…”
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4
A novel explanation for fluctuations of ion current through narrow pores
Published in The FASEB journal (01-06-1997)“…Fluctuation of ion current, between a high conductance and a low conductance state, through biological ion channels and pores is assumed to arise from…”
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5
Influence of pH on the uptake of 5-fluorouracil into isolated tumour cells
Published in British journal of cancer (01-03-1998)“…To investigate the possible dependence of 5-fluorouracil (5FU) uptake in tumours on the intra- (pHi) and extracellular (pHe) pH, a pH gradient (deltapH) was…”
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6
Rapid Switching of Ion Current in Narrow Pores: Implications for Biological Ion Channels
Published in Proceedings of the Royal Society. B, Biological sciences (22-06-1993)“…Ions flowing through purely synthetic filters made of polyethylene terephathalate which have been etched to produce narrow pores show: (i) rapid transitions…”
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Membrane damage by hemolytic viruses, toxins, complement, and other cytotoxic agents. A common mechanism blocked by divalent cations
Published in The Journal of biological chemistry (15-07-1986)“…Hemolytic viruses, bacterial and animal toxins, the components of activated complement, cationic proteins, and detergents induce a sequence of permeability…”
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8
Thermal control of drug release by a responsive ion track membrane observed by radio tracer flow dialysis
Published in Journal of controlled release (02-01-1998)“…The combination of a responsive hydrogel with a rigid porous supporting structure yields a membrane with high mechanical strength and high on-off-permeability…”
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9
Low conductance states of a single ion channel are not 'closed'
Published in The Journal of membrane biology (01-10-1995)“…We have used a polymer-exclusion method to estimate the sizes of the high- and low-conductance states of Staphylococcus aureus alpha-toxin channels across…”
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10
Scanning ion conductance microscopy of living cells
Published in Biophysical journal (01-08-1997)“…Currently there is a great interest in using scanning probe microscopy to study living cells. However, in most cases the contact the probe makes with the soft…”
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11
Triton channels are sensitive to divalent cations and protons
Published in The Journal of membrane biology (01-07-1994)“…Addition of Triton X-100 to planar bilayers composed of dioleoyl phosphatidyl choline, diphytanoyl phosphatidyl choline or mono-oleoyl glycerol induces single…”
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12
Divalent cation-sensitive pores formed by natural and synthetic melittin and by Triton X-100
Published in Biochimica et biophysica acta (09-01-1991)“…Leakage of ions and low-molecular-weight metabolites from Lettre cells is induced by synthetic melittin, as effectively as by melittin isolated from bee venom;…”
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13
Differential sensitivity of pneumolysin-induced channels to gating by divalent cations
Published in The Journal of membrane biology (01-05-1992)“…The induction of channels across planar lipid bilayers by purified, recombinant pneumolysin (a hemolytic protein from Streptococcus pneumoniae) has been…”
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14
Diffusion through narrow pores: movement of ions, water and nonelectrolytes through track-etched PETP membranes
Published in The Journal of membrane biology (01-05-1996)“…The rates at which ions (86Rb+, [3H]-choline, 36Cl), 3H2O and nonelectrolytes ([14C]-urea, [14C]-glycerol, and [14C]-sugars) equilibrate across track-etched…”
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15
Pore-forming toxins: experiments with S. aureus alpha-toxin, C. perfringens theta-toxin and E. coli haemolysin in lipid bilayers, liposomes and intact cells
Published in Toxicon (Oxford) (1990)“…Three quite different bacterial toxins (S. aureus alpha-toxin, C. perfringens theta-toxin and E. coli haemolysin) induce the leakage of phosphorylated…”
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Staphylococcus aureus alpha-toxin-induced pores: channel-like behavior in lipid bilayers and patch clamped cells
Published in The Journal of membrane biology (01-01-1995)“…The conductance of pores induced by Staphylococcus aureus alpha-toxin in Lettre cells has been compared to that in bilayers composed of synthetic lipids or…”
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Pore formation by S. aureus alpha-toxin in liposomes and planar lipid bilayers: effects of nonelectrolytes
Published in The Journal of membrane biology (01-03-1996)“…Nonelectrolytes such as polyethylene glycols (PEG) and dextrans (i) promote the association of S. aureus alpha-toxin with liposomes (shown by Coomassie…”
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18
Cell damage by cytolysin. Spontaneous recovery and reversible inhibition by divalent cations
Published in The Journal of immunology (1950) (01-12-1988)“…Cytolysin-induced membrane damage (which requires low Ca2+) has been studied 1) in E by assay of hemolysis, 2) in Lettre cells by measurement of transmembrane…”
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Ion modulation of membrane permeability: effect of cations on intact cells and on cells and phospholipid bilayers treated with pore-forming agents
Published in The Journal of membrane biology (01-07-1988)“…Leakage of ions (Na+, K+) and phosphorylated metabolites (phosphorylcholine, 2-deoxyglucose 6-phosphate) through membrane lesions in intact cells or in cells…”
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Plasma membrane potential of Lettré cells does not depend on cation gradients but on pumps
Published in The Journal of membrane biology (01-01-1984)“…The plasma membrane potential of Lettré cells has been determined with the optical indicator oxonol-V and found to be -57 mV at 37 degrees C (range -20 to -80…”
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