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1.
Phytomedicine ; 14(6): 377-80, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17140782

ABSTRACT

The present study was designated to evaluate the antileishmanial activity of acid and basic fractions that were obtained after acid-basic extraction, from ethanolic 70% crude extract and pure compounds from the stem bark of Aspidosperma ramiflorum. The basic alkaloidal fraction presented a good activity against the extracellular form (promastigotes) of Leishmania (L.) amazonensis (LD(50) value<47 microg/ml). Based on these findings, the basic fraction was fractionated on silica gel column chromatography in a bioassay-guided fractionation affording individual purified ramiflorines A and B. Both ramiflorines A and B showed significant activity against Leishmania (L.) amazonensis (LD(50) values of 16.3+/-1.6 microg/ml and 4.9+/-0.9 microg/ml, respectively). Our results are promising, showing that these compounds are biologically active against Gram-positive bacteria.


Subject(s)
Antiprotozoal Agents/pharmacology , Aspidosperma/chemistry , Indole Alkaloids/pharmacology , Leishmania/drug effects , Animals , Antiprotozoal Agents/chemistry , Indole Alkaloids/chemistry , Molecular Conformation , Phytotherapy , Plant Bark/chemistry , Plant Stems/chemistry
2.
Braz. j. med. biol. res ; 39(3): 387-391, Mar. 2006. ilus, graf
Article in English | LILACS | ID: lil-421371

ABSTRACT

We evaluated the antibacterial activities of the crude methanol extract, fractions (I-V) obtained after acid-base extraction and pure compounds from the stem bark of Aspidosperma ramiflorum. The minimum inhibitory concentration (MIC) was determined by the microdilution technique in Mueller-Hinton broth. Inoculates were prepared in this medium from 24-h broth cultures of bacteria (10(7) CFU/mL). Microtiter plates were incubated at 37°C and the MICs were recorded after 24 h of incubation. Two susceptibility endpoints were recorded for each isolate. The crude methanol extract presented moderate activity against the Gram-positive bacteria B. subtilis (MIC = 250 µg/mL) and S. aureus (MIC = 500 µg/mL), and was inactive against the Gram-negative bacteria E. coli and P. aeruginosa (MIC > 1000 µg/mL). Fractions I and II were inactive against standard strains at concentrations of <=1000 µg/mL and fraction III displayed moderate antibacterial activity against B. subtilis (MIC = 500 µg/mL) and S. aureus (MIC = 250 µg/mL). Fraction IV showed high activity against B. subtilis and S. aureus (MIC = 15.6 µg/mL) and moderate activity against E. coli and P. aeruginosa (MIC = 250 µg/mL). Fraction V presented high activity against B. subtilis (MIC = 15.6 µg/mL) and S. aureus (MIC = 31.3 µg/mL) and was inactive against Gram-negative bacteria (MIC > 1000 µg/mL). Fractions III, IV and V were then submitted to bioassay-guided fractionation by silica gel column chromatography, yielding individual purified ramiflorines A and B. Both ramiflorines showed significant activity against S. aureus (MIC = 25 µg/mL) and E. faecalis (MIC = 50 µg/mL), with EC50 of 8 and 2.5 µg/mL for ramiflorines A and B, respectively, against S. aureus. These results are promising, showing that these compounds are biologically active against Gram-positive bacteria.


Subject(s)
Anti-Bacterial Agents/pharmacology , Aspidosperma/chemistry , Indole Alkaloids/pharmacology , Anti-Bacterial Agents/chemistry , Bacillus subtilis/drug effects , Dose-Response Relationship, Drug , Escherichia coli/drug effects , Indole Alkaloids/chemistry , Microbial Sensitivity Tests , Plant Extracts/pharmacology , Pseudomonas aeruginosa/drug effects
3.
Braz J Med Biol Res ; 39(3): 387-91, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16501818

ABSTRACT

We evaluated the antibacterial activities of the crude methanol extract, fractions (I-V) obtained after acid-base extraction and pure compounds from the stem bark of Aspidosperma ramiflorum. The minimum inhibitory concentration (MIC) was determined by the microdilution technique in Mueller-Hinton broth. Inoculates were prepared in this medium from 24-h broth cultures of bacteria (10(7) CFU/mL). Microtiter plates were incubated at 37 masculineC and the MICs were recorded after 24 h of incubation. Two susceptibility endpoints were recorded for each isolate. The crude methanol extract presented moderate activity against the Gram-positive bacteria B. subtilis (MIC = 250 microg/mL) and S. aureus (MIC = 500 microg/mL), and was inactive against the Gram-negative bacteria E. coli and P. aeruginosa (MIC > 1000 microg/mL). Fractions I and II were inactive against standard strains at concentrations of < or =1000 microg/mL and fraction III displayed moderate antibacterial activity against B. subtilis (MIC = 500 microg/mL) and S. aureus (MIC = 250 microg/mL). Fraction IV showed high activity against B. subtilis and S. aureus (MIC = 15.6 microg/mL) and moderate activity against E. coli and P. aeruginosa (MIC = 250 microg/mL). Fraction V presented high activity against B. subtilis (MIC = 15.6 microg/mL) and S. aureus (MIC = 31.3 microg/mL) and was inactive against Gram-negative bacteria (MIC > 1000 microg/mL). Fractions III, IV and V were then submitted to bioassay-guided fractionation by silica gel column chromatography, yielding individual purified ramiflorines A and B. Both ramiflorines showed significant activity against S. aureus (MIC = 25 microg/mL) and E. faecalis (MIC = 50 microg/mL), with EC50 of 8 and 2.5 microg/mL for ramiflorines A and B, respectively, against S. aureus. These results are promising, showing that these compounds are biologically active against Gram-positive bacteria.


Subject(s)
Anti-Bacterial Agents/pharmacology , Aspidosperma/chemistry , Indole Alkaloids/pharmacology , Anti-Bacterial Agents/chemistry , Bacillus subtilis/drug effects , Dose-Response Relationship, Drug , Escherichia coli/drug effects , Indole Alkaloids/chemistry , Microbial Sensitivity Tests , Plant Extracts/pharmacology , Pseudomonas aeruginosa/drug effects
4.
Biochemistry ; 40(25): 7464-73, 2001 Jun 26.
Article in English | MEDLINE | ID: mdl-11412099

ABSTRACT

The eukaryotic cyclic nucleotide-gated (CNG) ion channels are a family of large membrane proteins activated by cytoplasmic cGMP or cAMP. Their cyclic nucleotide-binding domain is structurally homologous with that of the catabolite gene-activator protein (CAP), a soluble Escherichia coli transcription factor. Differences in ligand activation among sensory channels suggest differences in the underlying molecular mechanisms of signal readout. To study the structural, functional, and conformational consequences of nucleotide binding, we fused the cyclic nucleotide-binding domain from the bovine retinal rod CNG channel alpha subunit (Bralpha) to the DNA-binding domain from CAP. The chimera forms a soluble dimer that binds both cGMP and cAMP with association constants of 3.7 x 10(4) M(-1) for [(3)H]cGMP and 3.1 x 10(4) M(-1) for [(3)H]cAMP. The binding of cAMP, but not cGMP, exposes a chymotrypsin cleavage site in the chimera at a position similar to the site in the CAP exposed by cAMP binding. At high cAMP concentrations, a biphasic pattern of cleavage is seen, suggesting that the low-affinity cAMP binding sites are also occupied. Cyclic AMP promotes specific binding to a DNA fragment encoding the lac operator region; the K(d) for the protein-DNA binding is approximately 200 nM, which is 2-fold higher than the K(d) for CAP under identical conditions. A 7 A crystal structure shows that the overall secondary and tertiary structure of Bralpha/CAP is the same as that of CAP with two cAMP molecules bound per dimer. The biochemical characterization of the chimera suggests it will be a useful system for testing hypotheses about channel activation, providing further insight into channel function.


Subject(s)
Cyclic AMP Receptor Protein/genetics , DNA-Binding Proteins/genetics , Ion Channels/genetics , Ion Channels/metabolism , Recombinant Fusion Proteins/physiology , Rod Cell Outer Segment/physiology , Amino Acid Sequence , Animals , Bacterial Proteins/chemistry , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Cattle , Chymotrypsin/metabolism , Crystallography, X-Ray , Cyclic AMP/metabolism , Cyclic AMP Receptor Protein/chemistry , Cyclic AMP Receptor Protein/metabolism , Cyclic Nucleotide-Gated Cation Channels , DNA/metabolism , DNA-Binding Proteins/metabolism , Dimerization , Escherichia coli/genetics , Genetic Vectors/chemical synthesis , Hydrolysis , Molecular Sequence Data , Protein Binding/genetics , Protein Conformation , Protein Structure, Tertiary/genetics , Recombinant Fusion Proteins/biosynthesis , Recombinant Fusion Proteins/isolation & purification , Recombinant Fusion Proteins/metabolism , Solubility , Structure-Activity Relationship
5.
Biophys J ; 78(5): 2321-33, 2000 May.
Article in English | MEDLINE | ID: mdl-10777730

ABSTRACT

Cyclic nucleotide-gated (CNG) channels, which were initially studied in retina and olfactory neurons, are activated by cytoplasmic cGMP or cAMP. Detailed comparisons of nucleotide-activated currents using nucleotide analogs and mutagenesis revealed channel-specific residues in the nucleotide-binding domain that regulate the binding and channel-activation properties. Of particular interest are N(1)-oxide cAMP, which does not activate bovine rod channels, and Rp-cGMPS, which activates bovine rod, but not catfish, olfactory channels. Previously, we showed that four residues coordinate the purine interactions in the binding domain and that three of these residues vary in the alpha subunits of the bovine rod, catfish, and rat olfactory channels. Here we show that both N(1)-oxide cAMP and Rp-cGMPS activate rat olfactory channels. A mutant of the bovine rod alpha subunit, substituted with residues from the rat olfactory channel at the three variable positions, was weakly activated by N(1)-oxide cAMP, and a catfish olfactory-like bovine rod mutant lost activation by Rp-cGMPS. These experiments underscore the functional importance of purine contacts with three residues in the cyclic nucleotide-binding domain. Molecular models of nucleotide analogs in the binding domains, constructed with AMMP, showed differences in the purine contacts among the channels that might account for activation differences.


Subject(s)
Ion Channels/genetics , Ion Channels/metabolism , Nucleotides, Cyclic/metabolism , Retinal Rod Photoreceptor Cells/metabolism , Animals , Binding Sites/genetics , Biophysical Phenomena , Biophysics , Catfishes , Cattle , Cyclic GMP/analogs & derivatives , Cyclic GMP/metabolism , Cyclic Nucleotide-Gated Cation Channels , Humans , In Vitro Techniques , Ion Channels/chemistry , Ligands , Models, Molecular , Mutagenesis, Site-Directed , Olfactory Receptor Neurons/metabolism , Protein Structure, Secondary , Protein Structure, Tertiary , Rats , Recombinant Proteins/chemistry , Recombinant Proteins/genetics , Recombinant Proteins/metabolism
6.
Biochim Biophys Acta ; 1476(2): 350-62, 2000 Feb 09.
Article in English | MEDLINE | ID: mdl-10669799

ABSTRACT

A 114 kDa, water-soluble, cytotoxin secreted by the Gram-negative bacterium Actinobacillus actinomycetemcomitans (Aa) is similar in sequence to Escherichia coli alpha-hemolysin, but is non-hemolytic, killing leukocytes of select species, including humans. In this work, we investigated aspects of the water-soluble conformation of Aa toxin which relate to its biological, pore-forming activity. The toxin has five native tryptophans and fluorescence spectra were monitored in aqueous solutions in the presence of varying denaturants. Significant changes in the fluorescence spectra, without significant wavelength shifts, were induced by small additions of denaturants and changes in the temperature or pH. The fluorescence changes suggested that small perturbations in the aqueous environment resulted in structural changes in the toxin related not to a large unfolding but to more subtle conformational changes. Analytical ultracentrifugation showed the toxin to be a globular monomer in dilute aqueous solution. Circular dichroism spectroscopy showed about 25% alpha-helical structure which is largely maintained up to a temperature (65 degrees C) known to deactivate toxin activity. Changes in the cytotoxic properties of the toxin were monitored with flow cytometric analysis following preincubation of the toxin under mild conditions similar to those used in the fluorescence studies. These experiments showed that the pretreated toxin exhibited enhanced cell-killing potency on toxin-sensitive cells. The correlation of cytotoxicity with the changes in Trp fluorescence is consistent with the idea that partial unfolding of Aa toxin is an early, obligate step in toxin-induced cell kill.


Subject(s)
Aggregatibacter actinomycetemcomitans/metabolism , Exotoxins/chemistry , Bacterial Toxins/chemistry , Bacterial Toxins/metabolism , Escherichia coli , Exotoxins/metabolism , Fluorescence , Protein Conformation , Protein Denaturation
7.
Brain Res Bull ; 48(6): 641-7, 1999 Apr.
Article in English | MEDLINE | ID: mdl-10386845

ABSTRACT

Ibogaine has been shown to affect biogenic amine levels in selected brain regions. Because of the involvement of these neurotransmitters in drug addiction, the effects of ibogaine on biogenic amine transport may contribute to the potential anti-addictive properties of ibogaine in vivo. With rat brain synaptosomes as our experimental system, we measured the effects of ibogaine on the uptake and release of dopamine (DA) and serotonin (5-HT). Ibogaine competitively blocked both DA and 5-HT uptake with IC50 values of 20 microM at 75 nM 3H-DA and 2.6 microM at 10 nM 3H-5-HT. Ibogaine had no effect on K+-induced release of 3H-DA from preloaded synaptosomes, but 20 microM and 50 microM ibogaine inhibited roughly 40% and 60%, respectively, of the K(+)-induced release of 3H-5-HT from preloaded synaptosomes. In the absence of a depolarizing stimulus, ibogaine evoked a small release of 3H-DA but not 3H-5-HT. These relatively low-potency effects of ibogaine on DA and 5-HT uptake in synaptosomes are consistent with the low binding affinity of ibogaine that has been previously reported for DA and 5-HT transporters. Our results show that if ibogaine modulates DA and 5-HT levels in the brain by directly blocking their uptake, then a concentration of ibogaine in the micromolar range is required. Furthermore, if the anti-addictive effects of ibogaine require this concentration, then ibogaine likely exerts these effects through a combination of neurotransmitter pathways, because binding affinities and functional potencies of ibogaine in the micromolar range have been reported for a variety of neuronal receptors and transporters.


Subject(s)
Brain/metabolism , Dopamine/metabolism , Hallucinogens/pharmacology , Ibogaine/pharmacology , Serotonin/metabolism , Synaptosomes/metabolism , Animals , Biological Transport/drug effects , Brain/drug effects , Cerebral Cortex/drug effects , Cerebral Cortex/metabolism , Corpus Striatum/drug effects , Corpus Striatum/metabolism , Potassium/pharmacology , Rats , Rats, Wistar , Synaptosomes/drug effects
8.
Biochemistry ; 37(49): 17239-52, 1998 Dec 08.
Article in English | MEDLINE | ID: mdl-9860838

ABSTRACT

Cytoplasmic cAMP and cGMP are soluble cellular messengers that directly activate cyclic nucleotide-gated (CNG) channels. These channels mediate sensory transduction in photoreceptors and olfactory neurons. The closely related CNG channels in these cell types have different nucleotide activation profiles, and we have investigated the molecular basis of their nucleotide selectivity properties. Previously, we predicted that the purine moiety of the nucleotide interacts with residues F533, K596, and D604 (bovine rod alpha CNG channel subunit sequences) of the nucleotide binding domain. In this study, we replaced these three residues with the corresponding residues of the bovine olfactory CNG channel. Mutations at each position altered the nucleotide activation of the rod CNG channels. In a mutant where K596 was replaced with arginine, cAMP-activated currents were enhanced 8-12-fold, suggesting that residue 596 influences channel gating. Thermodynamic cycle analysis of the data showed that (1) the residues are energetically coupled and (2) energetic coupling exists between the potentiating effects of Ni2+ and the replacement of F533 with tyrosine. These data suggest that changes in one of the residues alter the purine contacts with the other residues and that F533 communicates with the C-linker region of the channel involved in Ni2+ potentiation.


Subject(s)
Amino Acids/metabolism , Ion Channels/metabolism , Models, Molecular , Purine Nucleotides/metabolism , Rod Cell Outer Segment/metabolism , Amino Acid Substitution/genetics , Animals , Aspartic Acid/genetics , Aspartic Acid/metabolism , Cattle , Cyclic GMP/genetics , Cyclic GMP/metabolism , Cyclic Nucleotide-Gated Cation Channels , Evoked Potentials/drug effects , Ion Channels/genetics , Ligands , Lysine/genetics , Lysine/metabolism , Mutagenesis, Site-Directed , Nickel/pharmacology , Patch-Clamp Techniques , Phenylalanine/genetics , Phenylalanine/metabolism , Protein Binding/drug effects , Protein Binding/genetics , Protons
10.
Biochim Biophys Acta ; 1406(2): 175-87, 1998 Mar 05.
Article in English | MEDLINE | ID: mdl-9573356

ABSTRACT

The mechanism of cell death induced by Actinobacillus actinomycetemcomitans leukotoxin (LTX) has been investigated with flow cytometry and patch electrode recording using cultured HL60 cells. The kinetics of propidium iodide (PI) positive staining of HL60 cells was measured as a function of LTX concentration at 37 degreesC. Results showed a concentration-dependent decrease in the tk times. Cell kill was slow at <1 microg/ml LTX concentrations with fewer than 50% of the cells killed after 1 h; at 1 microg/ml, the tk times ranged from approximately 15 to 30 min. At higher concentrations, the tk times decreased rapidly. The rate of cell kill was appreciably slowed at 20 degreesC. HL60 whole cell currents were recorded with patch electrodes. Immediately following exposure to high concentrations of LTX, large currents were recorded suggesting that the membrane potential of these cells had collapsed due to the large conductance increases. At low toxin concentrations, rapid conductance fluctuations were seen suggestive of a limited number of toxin-mediated events. Cells exposed to low concentrations of LTX exhibited these conductance fluctuations for up to 1 h, whereas toxin-insensitive cells were unaffected by long exposures to high concentrations of toxin. Our results are consistent with LTX-induced pores in susceptible cells which overwhelm the ability of the cell to maintain osmotic homeostasis causing cell death.


Subject(s)
Aggregatibacter actinomycetemcomitans , Bacterial Toxins/pharmacology , Cytotoxins/pharmacology , Exotoxins/pharmacology , Ion Channels/metabolism , Cell Death , Electric Conductivity , Flow Cytometry , Humans , Kinetics , Patch-Clamp Techniques , Tumor Cells, Cultured
11.
Biophys J ; 72(1): 127-40, 1997 Jan.
Article in English | MEDLINE | ID: mdl-8994598

ABSTRACT

We developed a two-site, Eyring rate theory model of ionic permeation for cyclic nucleotide-gated channels (CNGCs). The parameters of the model were optimized by simultaneously fitting current-voltage (IV) data sets from excised photoreceptor patches in electrolyte solutions containing one or more of the following ions: Na+, Ca2+, Mg2+, and K+. The model accounted well for 1) the shape of the IV relations; 2) the binding affinity for Na+; 3) reversal potential values with single-sided additions of Ca2+ or Mg2+ and biionic KCl; and 4) the K1 and voltage dependence for divalent block from the cytoplasmic side of the channel. The differences between the predicted K1's for extracellular block by Ca2+ and Mg2+ and the values obtained from heterologous expression of only the alpha-subunit of the channel suggest that the beta-subunit or a cell-specific factor affects the interaction of divalent cations at the external but not the internal face of the channel. The model predicts concentration-dependent permeability ratios with single-sided addition of Ca2+ and Mg2+ and anomalous mole fraction effects under a limited set of conditions for both monovalent and divalent cations. Ca2+ and Mg2+ are predicted to carry 21% and 10%, respectively, of the total current in the retinal rod cell at -60 mV.


Subject(s)
Cyclic GMP/pharmacology , Ion Channels/physiology , Retinal Rod Photoreceptor Cells/physiology , Ambystoma , Animals , Calcium/metabolism , Calcium/pharmacology , Cell Membrane Permeability , In Vitro Techniques , Ion Channels/drug effects , Kinetics , Macromolecular Substances , Magnesium/pharmacology , Mathematics , Membrane Potentials/drug effects , Models, Biological , Patch-Clamp Techniques , Potassium Chloride/pharmacology , Rana pipiens , Retinal Rod Photoreceptor Cells/drug effects , Sodium/metabolism , Sodium/pharmacology
12.
Protein Eng ; 9(4): 333-44, 1996 Apr.
Article in English | MEDLINE | ID: mdl-8738209

ABSTRACT

Cyclic nucleotide-gated channels (CNGC) open in response to the binding of 3'5'-cyclic nucleotides. Members of the CNGC family vary as much as 100-fold in their ability to respond to cAMP and cGMP. Molecular models of the nucleotide binding domains of the bovine retina and catfish and rat olfactory CNGCs were built from the crystal structure of cAMP bound to catabolite gene activator protein (CAP) with AMMP, a program for molecular mechanics and dynamics. The nucleotide conformation can be predicted from the number of strong and weak interactions between the purine ring and the binding site. The amino acids predicted to be important for determining the nucleotide affinity and specificity are residues 61, 83 (mediated through a water molecule), 119 and 127 (CAP sequence numbers) which interact with the purine ring. These residues also dictate the conformation of the ligand in the binding pocket. cGMP is preferentially bound in the syn conformation in bovine retina, bovine olfactory and rat olfactory CNGCs due to Thr83, while either conformation can bind in catfish olfactory CNGC. cAMP is predicted to bind either in syn or anti conformation, depending on the interaction with residue 119: the anti conformation is preferentially bound in olfactory CNGCs.


Subject(s)
Ion Channel Gating , Ion Channels/metabolism , Nucleotides, Cyclic/metabolism , Olfactory Mucosa , Retina , Animals , Binding Sites , Catfishes , Cattle , Computer Simulation , Cyclic GMP/metabolism , Cyclic Nucleotide-Gated Cation Channels , Forecasting , Ligands , Models, Molecular , Molecular Conformation , Rats , Recombinant Fusion Proteins
13.
Biochim Biophys Acta ; 1240(2): 149-58, 1995 Dec 13.
Article in English | MEDLINE | ID: mdl-8541286

ABSTRACT

Magainin 1 and magainin 2 are broad-spectrum antimicrobial and antifungal peptides initially purified from Xenopus laevis skin glands. The mechanism of cytotoxicity of the naturally occurring magainin 2 and a potent all-D amino acid analogue, MSI-238, was examined for eukaryotic cells using flow cytometric analysis with propidium iodide (PI). Exposure to MSI-238 resulted in cell death within seconds to minutes, depending on the concentration of the peptide. Several cell types were examined including a mouse fibroblast cell line Balb/3T3 and a Rous sarcoma virus Balb/3T3-transformed cell line, SRD/3T3, primary chick embryo fibroblasts and cells derived from a human ovarian carcinoma, OVCA-3. The K0.5 values determined from 5 min exposures ranged from 24 to 80 micrograms/ml for MSI-238 and approximately 600 micrograms/ml for magainin 2. Molecular properties of MSI-238 induced channels were studied in excised membrane patch recordings from Balb/3T3 and SRD/3T3 cells. At low concentrations of 0.1 micrograms/ml, occasional, brief, multiple-level current fluctuations were seen suggesting channels with multiple, rapidly changing conductance levels. At 5 or 10 micrograms/ml of MSI-238, the current fluctuations were larger in magnitude and occurred more frequently producing a general disruption of the membrane similar to the effects of melittin on membranes.


Subject(s)
3T3 Cells/drug effects , Anti-Infective Agents/pharmacology , Antimicrobial Cationic Peptides , Peptides/pharmacology , Xenopus Proteins , Animals , Cell Cycle/drug effects , Cell Death/drug effects , Cell Line, Transformed , Chick Embryo , Dose-Response Relationship, Drug , Fibroblasts , Humans , Magainins , Mice , Patch-Clamp Techniques , Tumor Cells, Cultured
14.
Biochim Biophys Acta ; 1238(1): 34-41, 1995 Aug 23.
Article in English | MEDLINE | ID: mdl-7544624

ABSTRACT

Actinobacillus actinomycetemcomitans leukotoxin is a member of the bacterial RTX (repeats in toxin) toxin family, produced by a diverse group of Gram-negative pathogens. Members of this group of toxins, although similar in sequence, differ in target cell specificity with Actinobacillus actinomycetemcomitans leukotoxin demonstrating a unique species- and cell-type specificity. Purified A. actinomycetemcomitans leukotoxin added to pre-formed POPE/POPS lipid bilayers showed no spontaneous incorporation (to concentrations of 250 ng/ml). Reproducible channel activity was seen when the bilayer was reformed from lipid monolayers in the presence of toxin (50 ng/ml) in one of the aqueous chambers. Control experiments with heat-inactivated toxin did not display channel activity under the same experimental conditions. The channel behavior showed a complex pattern of multiple conductance levels of 118, 262 and 406 pS in solutions containing 0.140 M NaCl. The first two states showed voltage-dependent channel gating with approximately equal but opposite apparent gating charges of 1.4 electrons. A model accounting for the multiple conducting states and gating properties is presented.


Subject(s)
Aggregatibacter actinomycetemcomitans/pathogenicity , Bacterial Toxins/metabolism , Exotoxins/metabolism , Ion Channel Gating , Ion Channels/metabolism , Lipid Bilayers/metabolism
15.
Biochemistry ; 34(7): 2338-47, 1995 Feb 21.
Article in English | MEDLINE | ID: mdl-7532007

ABSTRACT

Photoreceptor outer segments transduce information about incoming light levels through a class of ion channels that respond directly to changes in cytosolic 3',5'-cyclic guanosine monophosphate levels. A series of 3',5'-cyclic purine analogues with alterations at N1, C2, C6, or C8 positions was used to examine molecular interactions between the nucleotide and the channel. The maximal current activated by C2-altered analogues in excised membrane patches was less than the current activated by cGMP, and the K0.5, the concentration which activates 50% of the current in a patch, was increased. Nonpolar C8-substituted cAMP analogues activated more current than the parent cAMP with lower K0.5 values. This was in contrast to 8-amino-cAMP, which exhibited greatly reduced activity. The rank order of activity, based on K0.5 values, for C8-cAMP substituents was as follows: 8-azido- > 8-methylamino- > 8-benzylamino- > cAMP > 8-bromo- > 8-hydroxy- >> 8-amino-cAMP. 1,N6-Etheno-cAMP and N6-monobutyryl-cAMP activated a small fraction of the total possible current with high K0.5 values. Other analogues with alterations at N1 or C6 positions including N1-oxide-cAMP, 2-aminopurine riboside 3',5'-monophosphate, and N6-monosuccinyl-cAMP do not bind to the channel, suggesting that interactions with the channel in this region are essential for binding. In order to help interpret the changes in maximal current and K0.5 values compared to cGMP, molecular models of the active analogues were constructed and then docked into a molecular model of the cyclic nucleotide binding site of the retinal channel. This model, proposed by Kumar and Weber [(1992) Biochemistry 31, 4643-4649], was based on the crystal structure of cAMP bound to catabolite activator protein. Our modeling showed that the analogues were sterically accommodated within the binding site. No hydrogen bonds were predicted between the purine rings of cAMP and the pocket; however, Phe 533 on the beta 5 strand was predicted to form weak electrostatic interactions with C6 substituents on both cAMP and cGMP. The importance of contacts in this region of the binding pocket is further emphasized by the inactive analogues, all of which are altered at N1 or C6.


Subject(s)
Cyclic GMP/analogs & derivatives , Cyclic GMP/metabolism , Eye Proteins/metabolism , Ion Channels/metabolism , Rod Cell Outer Segment/physiology , Ambystoma , Animals , Binding Sites , Computer Simulation , Cyclic Nucleotide-Gated Cation Channels , In Vitro Techniques , Ion Channel Gating , Ligands , Models, Molecular , Molecular Structure , Signal Transduction , Structure-Activity Relationship
16.
Biophys J ; 65(6): 2517-23, 1993 Dec.
Article in English | MEDLINE | ID: mdl-7508764

ABSTRACT

Macroscopic 3',5'-guanine cyclic monophosphate (cGMP)-activated currents from photoreceptor outer segment membranes were examined as the pH on the cytoplasmic face of inside/out patches was reduced. In the absence of divalent cations, protons reduced the current in both directions without affecting the shape of the current-voltage relation consistent with a voltage-independent block. When Ca2+ was added to the bath, increasing the [H+] relieved the Ca2+ block and eliminated the Ca(2+)-induced reversal potential shifts seen at pH 7.4. These results suggest that protons alter Na+/Ca2+ permeability of the channel and relieve Ca2+ block of the sodium transport.


Subject(s)
Cyclic GMP/pharmacology , Hydrogen-Ion Concentration , Ion Channels/physiology , Rod Cell Outer Segment/physiology , Animals , Calcium/pharmacology , Calcium Channels/drug effects , Calcium Channels/physiology , Cations, Divalent/pharmacology , In Vitro Techniques , Ion Channels/drug effects , Membrane Potentials/drug effects , Photoreceptor Cells/drug effects , Photoreceptor Cells/physiology , Protons , Rana pipiens , Rod Cell Outer Segment/drug effects , Sodium Channels/drug effects , Sodium Channels/physiology
17.
Biophys J ; 65(1): 552-8, 1993 Jul.
Article in English | MEDLINE | ID: mdl-8369460

ABSTRACT

Several strategies directed toward increasing the participation of minority students in physics and biophysics are presented. Since the number of minority students entering college with an interest in science and mathematics must be increased if we expect to see more students graduating in science, several programs aimed at increasing the level of instruction of physics and biology in urban middle schools and high schools are outlined. We also describe approaches designed to increase the retention of science major during the freshman core physics course where many potential science majors are lost. Increasing the number of minority students at the PhD level will rely increasingly on partnerships between research universities and historically black colleges and universities (HBCUs) and several programs already in effect are given as examples of such linkages.


Subject(s)
Biophysics/education , Physics/education , Minority Groups/education , Research/education , Teaching , United States
18.
J Membr Biol ; 131(3): 245-56, 1993 Feb.
Article in English | MEDLINE | ID: mdl-7684086

ABSTRACT

The light-sensitive current in photoreceptors is conducted by a single class of ion channels gated by the binding of multiple molecules of cytoplasmic cGMP. Both Na and Ca ions enter the outer segment through this channel and Ca behaves as a blocking ion, greatly reducing the influx of Na. Because intracellular Ca functions as the cytosolic messenger for light adaptation, and this channel is the major entry point for Ca into the outer segment, we seek a better understanding of the selectivity properties of the channel and how they affect intracellular Ca levels. In these studies, we added divalent cations to the cytoplasmic face of an excised patch at constant, symmetrical [Na]. Our results suggest a novel high-affinity divalent binding site at the internal face of the channel. At constant low levels of cGMP, the addition of 10-100 nM cytoplasmic Ca or Mg attenuated the current 5- to 10-fold. There is also a low-affinity site, midway through the transmembrane field; saturation of this site reduces the divalent-free current approximately 100-fold. The presence of a high-affinity cytoplasmic site raises the question of whether Ca regulates the photoreceptor current through a direct interaction with the channel perhaps altering the channel selectivity or kinetics.


Subject(s)
Calcium/pharmacology , Cyclic GMP/physiology , Ion Channels/physiology , Magnesium/pharmacology , Photoreceptor Cells/physiology , Rana pipiens/physiology , Animals , Dose-Response Relationship, Drug , Ion Channel Gating/physiology , Membrane Potentials/physiology , Sodium/pharmacology
19.
J Gen Physiol ; 96(1): 57-82, 1990 Jul.
Article in English | MEDLINE | ID: mdl-1698914

ABSTRACT

Monovalent cation selectivity has been characterized for the 3',5'-cyclic guanosine monophosphate (cGMP)-activated channel in vertebrate photoreceptor outer segment plasma membranes without divalent cations. Macroscopic currents in excised, inside-out patches were activated with saturating concentrations of cGMP (200 microM). Using a bi-ionic protocol with symmetrical 120 mM ion concentrations across the membrane, alkali metal ions and certain organic cations were substituted for sodium on the cytoplasmic face. The relative permeabilities, determined from shifts in the reversal potential (Erev), were NH4 much greater than Na greater than guanidinium greater than K greater than Li greater than Rb greater than Cs (3.34: 1.0: 0.97: 0.93: 0.92: 0.74: 0.50, respectively). Erev's were also measured as a function of [Na], [NH4], and [Cs], and the slope of the relation was -59.8, -52.1, and -49.1 mV/decade, respectively. The slopes for NH4 and Cs differ significantly from the Nernst-Planck prediction of -58.2 mV/decade expected for a single ion channel. Relative permeabilities were also determined for the alkali metal series of ions with 20 mM ionic concentrations on both sides of the membrane. The permeability sequence at 20 mM was unchanged, but the relative permeability for NH4 and Cs deviated significantly from the measurements at 120 mM with 1.46 and 0.75 ratios, respectively. The dependence of Erev on absolute concentrations and the deviation from Nernst-Planck predictions are best explained by multi-ion occupancy of the cGMP-activated channel. Selectivity was also examined by comparing the conductance ratios as a function of potential.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Cyclic GMP/physiology , Ion Channels/physiology , Animals , Bufo marinus , Cations, Monovalent/pharmacology , Cell Membrane Permeability/drug effects , Cell Membrane Permeability/physiology , Energy Metabolism/drug effects , In Vitro Techniques , Membrane Potentials/drug effects , Rana catesbeiana , Rana pipiens , Rana temporaria , Sodium Channels/drug effects , Sodium Channels/physiology
20.
Biochemistry ; 28(7): 2776-84, 1989 Apr 04.
Article in English | MEDLINE | ID: mdl-2545237

ABSTRACT

Cyclic nucleotide activated sodium currents were recorded from photoreceptor outer segment membrane patches. The concentration of cGMP and structurally similar nucleotide derivatives was varied at the cytoplasmic membrane face; currents were generated at each concentration by the application of a voltage ramp. Nucleotide-activated currents were analyzed as a function of both concentration and membrane potential. For cGMP, the average K0.5 at 0 mV was 24 microM, and the activation was cooperative with an average Hill coefficient of 2.3. Of the nucleotide derivatives examined, only 8-[[(fluorescein-5-yl-carbamoyl)methyl]thio]-cGMP (8-Fl-cGMP) activated the channel at lower concentrations than cGMP with a K0.5 of 0.85 microM. The next most active derivative was 2-amino-6-mercaptopurine riboside 3',5'-monophosphate (6-SH-cGMP) which had a K0.5 of 81 microM. cIMP and cAMP had very high K0.5 values of approximately 1.2 mM and greater than 1.5 mM, respectively. All nucleotides displayed cooperativity in their response and were rapidly reversible. Maximal current for each derivative was compared to the current produced at 200 microM cGMP; only 8-Fl-cGMP produced an identical current. The partial agonists 6-SH-cGMP, cIMP, and cAMP activated currents which were approximately 90%, 80%, and 25% of the cGMP response, respectively. 5'-GMP, 2-aminopurine riboside 3',5'-monophosphate, and 2'-deoxy-cGMP produced no detectable current. The K0.5 values for cGMP activation, examined from -90 to +90 mV, displayed a weak voltage dependence of approximately 400 mV/e-fold; the index of cooperativity was independent of the applied field.(ABSTRACT TRUNCATED AT 250 WORDS)


Subject(s)
Cyclic GMP/analogs & derivatives , Cyclic GMP/pharmacology , Photoreceptor Cells/physiology , Retina/physiology , Sodium Channels/physiology , Animals , Bufo marinus , Cyclic AMP/pharmacology , Electric Conductivity , In Vitro Techniques , Kinetics , Mathematics , Models, Theoretical , Photoreceptor Cells/drug effects , Rana pipiens , Sodium Channels/drug effects , Structure-Activity Relationship
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