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C F Schmidt

Publications and source records attributed to C F Schmidt.

At least 37 records · Page 2Linked to original sources
PubMed1993

Direct observation of kinesin stepping by optical trapping interferometry.

Do biological motors move with regular steps? To address this question, we constructed instrumentation with the spatial and temporal sensitivity to resolve movement on a molecular scale. We deposited silica beads carrying single molecules of the motor protein kinesin on microtubules using optical tweezers and analysed their motion under controlled loads by interferometry. We find that kinesin moves with 8-nm steps.

Adenosine Triphosphate↗
PubMed1993

Existence of a flat phase in red cell membrane skeletons.

Biomolecular membranes display rich statistical mechanical behavior. They are classified as liquid in the absence of shear elasticity in the plane of the membrane and tethered (solid) when the neighboring molecules or subunits are connected and the membranes exhibit solid-like elastic behavior in the plane of the membrane. The spectrin skeleton of red blood cells was studied as a model tethered membrane. The static structure factor of the skeletons, measured by small-angle x-ray and light scattering, was fitted with a structure factor predicted with a model calculation. The model describes tethered membrane sheets with free edges in a flat phase, which is a locally rough but globally flat membrane configuration. The fit was good for large scattering vectors. The membrane roughness exponent, zeta, defined through h alpha L zeta, where h is the average amplitude of out-of-plane fluctuations and L is the linear membrane dimension, was determined to be 0.65 +/- 0.10. Computer simulations of model red blood cell skeletons also showed this flat phase. The value for the roughness exponent, which was determined from the scaling properties of membranes of different sizes, was consistent with that from the experiments.

Chemical Phenomena↗
PubMed1992

Conformation and elasticity of the isolated red blood cell membrane skeleton.

We studied the structure and elasticity of membrane skeletons from human red blood cells (RBCs) during and after extraction of RBC ghosts with nonionic detergent. Optical tweezers were used to suspend individual cells inside a flow chamber, away from all surfaces; this procedure allowed complete exchange of medium while the low-contrast protein network of the skeleton was observed by high resolution, video-enhanced differential interference-contrast (DIC) microscopy. Immediately following extraction in a 5 mM salt buffer, skeletons assumed expanded, nearly spherical shapes that were uncorrelated with the shapes of their parent RBCs. Judging by the extent of thermal undulations and by their deformability in small flow fields, the bending rigidity of skeletons was markedly lower than that of either RBCs or ghosts. No further changes were apparent in skeletons maintained in this buffer for up to 40 min at low temperatures (T less than 10 degrees C), but skeletons shrank when the ionic strength of the buffer was increased. When the salt concentration was raised to 1.5 M, shrinkage remained reversible for approximately 1 min but thereafter became irreversible. When maintained in 1.5 M salt buffer for longer periods, skeletons continued to shrink, lost flexibility, and assumed irregular shapes: this rigidification was irreversible. At this stage, skeletons closely resembled those isolated in standard bulk preparations. We propose that the transformation to the rigid, irreversibly shrunken state is a consequence of spectrin dimer-dimer reconnections and that these structural rearrangements are thermally activated. We also measured the salt-dependent size of fresh and bulk extracted skeletons. Our measurements suggest that, in situ, the spectrin tethers are flexible, with a persistence length of approximately 10 nm at 150 mM salt.

Elasticity↗
PubMed1992

Analysis of cholesterol in all lipoprotein classes by single vertical ultracentrifugation of fingerstick blood and controlled-dispersion flow analysis.

This new, highly sensitive analytical system, based on controlled dispersion of the flowing sample, gives a rapid, continuous, and direct analysis for cholesterol in all lipoprotein classes, separated by single vertical-spin density-gradient ultracentrifugation. In this Vertical Auto Profile-II fingerstick system, designated VAP-IIfs, a narrow-bore Teflon coil serves as the reactor with no segmentation of the analytical stream by air bubbles, in contrast to the Technicon AutoAnalyzer used in the VAP-I method. Concentrations of high-, low-, intermediate-, and very-low-density lipoprotein cholesterol and lipoprotein(a) cholesterol are determined by decomposing the spectrophotometric absorbance curve for the continuous analysis of the centrifuged sample, with use of software developed in this laboratory. Total cholesterol is determined from the total area under the absorbance curve. For assaying total cholesterol, the CV between aliquots within a rotor ranged from 1.35% to 3.15%; the CV between rotors was 2.45%. Because only 18 microL of sample is required, VAP-IIfs can be readily adapted to analysis for lipoprotein cholesterol profiles in capillary blood samples. Total cholesterol values by VAP-IIfs for fingerstick and venous samples from 23 subjects agreed well: slope = 1.01 (SD 0.03), intercept = -21 (SD 51) mg/L, Sy/x = 50 mg/L, and r = 0.992. Results by VAP-IIfs also correlated highly with results for duplicate samples analyzed at the Northwest Lipid Research Laboratories.

Cholesterol↗
PubMed1990

Multilayer adsorption of lysozyme on a hydrophobic substrate.

Macromolecular adsorption is known to occur as a complex process, often in a series of steps. Several models are discussed in the literature which describe the microscopic structure of the adsorbate. In the present study we investigated the adsorption of hen egg white lysozyme on alkylated silicon oxide surfaces. A combination of fluorescence excitation in the evanescent field and fluorescence recovery after photobleaching allowed us to measure the amount of adsorbed fluorescent lysozyme and the equilibrium exchange kinetics with molecules in solution. We found that a model with at least three classes of adsorbed molecules is necessary to describe the experimental results. A first layer is formed by the molecules which adsorb within a short time after the beginning of the incubation. These molecules make up approximately 65% of the final coverage. They are quasi-irreversibly adsorbed and do not measurably exchange with bulk molecules within one day even at temperatures up to 55 degrees C. A second layer, which reaches equilibrium only after several hours of incubation, shows a pronounced exchange with bulk molecules. The on-off kinetics show a distinct temperature dependence from which an activation barrier of delta E approximately 22 kcal/mol is derived. A third layer of molecules that exchange rapidly with the bulk can be seen to comprise approximately 10% of the total coverage. The exchange rate is on the order of fractions of a second. The binding of the latter two classes of adsorbed molecules is exothermic. From the temperature dependence of the coverage, the binding enthalpy of the slowly exchanging layer was estimated to be delta Hads approximately 3.8 kcal/mol. The second and third class of molecules remain enzymatically active as a muramidase, which was tested by the lysis of the cell walls of Micrococcus lysodeiktikus. The molecules in the first layer, on the other hand, showed no enzymatic activity.

4-Chloro-7-nitrobenzofurazan↗
PubMed1985

Studies of synthetic peptide analogs of the amphipathic helix. Structure of complexes with dimyristoyl phosphatidylcholine.

The amphipathic helix hypothesis for the lipid-associating domains of exchangeable plasma apolipoproteins has been further studied by analysis of the structure of the complexes formed between four synthetic peptide analogs of the amphipathic helix and dimyristoyl phosphatidylcholine (DMPC). Density gradient ultracentrifugation, negative stain electron microscopy, nondenaturing gradient gel electrophoresis, 1H NMR, high sensitivity differential scanning calorimetry, and circular dichroism were the techniques used in these studies. The two analogs Asp-Trp-Leu-Lys-Ala-Phe-Tyr-Asp-Lys-Val-Ala-Glu-Lys-Leu-Lys-Glu-Ala-Phe (18A) and 18A-Pro-18A whose sequences most strongly mimic native amphipathic sequences were found also most strongly to mimic apolipoprotein A-I in DMPC complex structure. The covalently linked dimer of the prototype amphipathic analog 18A, 18A-Pro-18A, appears to have greater lipid affinity than 18A. This presumably is the result of the cooperativity provided by two covalently linked lipid-associating domains in 18A-Pro-18A. The studies further suggest that the charge-reversed analog of the prototype 18A, reverse-18A, has the lowest lipid affinity of the four analogs studied and forms only marginally stable discoidal DMPC complexes. We postulate that this low lipid affinity is due predominantly, but not necessarily exclusively, to the lack of a hydrophobic contribution of lysine residues at the polar-nonpolar interface of reverse-18A versus 18A. The intermediate lipid affinity of des-Val10-18A, the fourth analog peptide, to produce a rank order of 18A-Pro-18A greater than 18A greater than des-Val10-18A greater than reverse-18A, supports this interpretation. Des-Val10-18A which has Val deleted from 18A has an amphipathic helical structure partially disrupted by the shift of 2 lysine residues away from the polar-nonpolar interface.

Amino Acid Sequence↗
PubMed1982

Solubilization of phosphatidylcholine bilayers by octyl glucoside.

The solubilization of large, unilamellar egg phosphatidylcholine vesicles by the nonionic detergent octyl glucoside (OG) was investigated by nuclear magnetic resonance (NMR), fluorescence anisotropy, turbidity, electron microscopy, and centrifugation followed by compositional analysis. The solubilization process is well described by the three-stage model previously proposed for other detergents. In stage I, the OG partitions between the bilayer and aqueous phases with a molar partition coefficient of 59 +/- 6. The presence of OG in the bilayers produces a small "fluidizing" effect, as indicated by changes in the NMR and fluorescence anisotropy parameters. A rearrangement that forms large mixed bilayers occurs in the latter part of stage I. Stage II, the conversion of detergent-saturated bilayers into mixed micelles, begins at a ratio of total OG concentration minus the critical micelle concentration to total phosphatidylcholine concentration of approximately 1.5 and continues until this ratio reaches about 3.0. The correction for the critical micelle concentration of the OG is necessary for comparison of experimental results obtained at different lipid concentrations. The mixed bilayer-mixed micelle interconversion is quantified by the centrifugation experiments and by 31P NMR. The agreement between the two methods is excellent. Advantages of the NMR method are discussed. In stage III, which was not studied in detail here, all of the phosphatidylcholine is present as mixed micelles. Evidence is presented that the various structures present in the dispersions are in equilibrium with one another during these experiments.

Fluorescence Polarization↗
PubMed1982

Effect of cytochrome b5 on the transbilayer distribution of phospholipids in model membranes.

The transbilayer distribution of phosphatidylethanolamine was assessed in phosphatidylcholine-phosphatidylethanolamine vesicles that contained various amounts of cytochrome b5. The small vesicles, made by sonication, and the large vesicles, made by ethanol injection, were fractionated by centrifugation before cytochrome b5 was asymmetrically incorporated into the bilayer. The mole ratio of phospholipid to protein ranged from 280 to 560 in the small vesicles and from 100 to 500 in the large vesicles. The phosphatidylethanolamine distribution, determined by chemical labeling with trinitrobenzenesulfonic acid, was assessed in vesicles the contained intact cytochrome b5 molecules and in vesicles where only the hydrophobic tail remained associated with the bilayer. At every phospholipid to protein ratio examined, the transbilayer distribution of phosphatidylethanolamine in either the small or large unilamellar vesicles was not significantly different from the distribution in control vesicles that contained no protein. Ethanol was added to some cytochrome b5-vesicle preparations (20% v/v) in an attempt to facilitate rearrangement of the phospholipids. No differences in the transbilayer distribution were observed. These results are discussed in terms of transbilayer equilibrium and the perturbation induced by the protein.

Cytochromes↗
PubMed1981

Transbilayer distribution in small unilamellar phosphatidylglycerol-phosphatidylcholine vesicles.

The transbilayer distribution of the phospholipids in small unilamellar vesicles comprised of egg phosphatidylglycerol (PG) and egg phosphatidylcholine (PC) was ascertained by 31P NMR. These vesicles, containing 10-75 mol % PG, were formed by sonication (pH 7.6) and fractionated by centrifugation. Data from spectra accumulated in the presence and absence of a paramagnetic shift reagent, Mn2+, indicated that the phospholipids are randomly arranged across the bilayer. The absence of compositional asymmetry, which contradicts earlier reports, is also exhibited by small unilamellar vesicles (50 mol % PG) prepared by the rapid ethanol injection method. Control experiments showed that Mn2+ did not induce fusion, permeate the vesicles, or cause the phospholipids to migrate across the bilayer. It has been proposed that the transbilayer distribution of charged phospholipids in membranes is a consequence of the different surface charge densities on the opposing sides of the membrane. Our results suggest that it is the difference in the effective polar headgroup volumes of the components rather than the net charge of one component that determines the packing constraints for mixtures of phospholipids with the same acyl chains, at least in highly curved bilayers.

Egg Yolk↗
PubMed1981

Vesicle- vesicle interactions in sonicated dispersions of dipalmitoylphosphatidylcholine.

The time course of the size transformation of sonicated small unilamellar dipalmitoylphosphatidylcholine vesicles at 23 degrees C has been followed with (31)P and (1)H nuclear magnetic resonance (NMR) spectroscopy. Comparison of these results with turbidity measurements indicates that vesicle aggregation, monitored by turbidity, and size transformation, followed by NMR, occur on distinctly different time scales. For lipid concentrations in the 5-50 mM range, aggregation takes place on a time scale of minutes, whereas size transformation takes many hours. Aggregation, unlike size transformation, can be reversed by increasing the temperature above the phospholipid phase transition temperature. Analysis of the (31)P NMR line shapes provides evidence for a model in which the small vesicles transform into the product vesicles [characterized by Schullery, S.E., Schmidt, C.F., Felgner, P., Tillack, T.W., & Thompson, T.E. (1980) Biochemistry 19, 3919] without producing significant amounts of intermediate-size vesicles. Kinetic analysis indicates that the size transformation is apparently second order. (1)H NMR data indicate that the rate of transformation is decreased if trivalent ions are added to the dispersions and also if the temperature is periodically increased above the transition temperature. Analysis of the latter experiment provides some evidence that vesicle aggregation is a necessary precursor to size transformation. It was also found that increasing the average vesicle size decreases the extent of transformation.

Kinetics↗
PubMed1981

Solid-state carbon-13 nuclear magnetic resonance of the lecithin gel to liquid-crystalline phase transition.

The temperature dependence of the 13C NMR spectra of dipalmitoylphosphatidylcholine (DPPC) which has been 13C labeled at the carbonyl position of the sn-2 chain, 2-[1-13C]DPPC, is reported. In the L beta' phase an axially symmetric spectrum of 112-ppm breadth is observed, and this transforms to an isotropic-like line ((delta sigma) approximately 7 ppm) in the L alpha phase. In the intermediate P beta phase a temperature-dependent superposition of these spectra is observed, which suggests that this phase exhibits microscopic structural and dynamical properties of both the L beta' and L alpha phases. An analysis of the spectral line shapes leads to the conclusion that the appearance of the isotropic-like line in the P beta' phase is primarily due to a conformational change at the sn-2 carbonyl which is complete at the main transition. Increased rates of axial diffusion in the P beta' phase may contribute to the narrowing.

Carbon Isotopes↗
PubMed1981

Effect of surface curvature on stability, thermodynamic behavior, and osmotic activity of dipalmitoylphosphatidylcholine single lamellar vesicles.

The size and surface curvature dependence of the properties and stability of single lamellar vesicles have been investigated by using a variety of physicochemical techniques. Dipalmitoylphosphatidylcholine single lamellar vesicles of sizes ranging between 200 and 900 A in diameter have been prepared by the French press method and characterized with respect to their size distribution, stability, and thermotropic behavior by negative stain electron microscopy, molecular sieve chromatography, nuclear magnetic resonance spectroscopy, and differential scanning calorimetry. Vesicles with a diameter smaller than 400 A are unstable below their transition temperature and fuse spontaneously to form larger single lamellar vesicles. Correlation analysis of experimentally obtained size distributions and calorimetric phase transitions profiles allowed estimation of the size dependence of the transition temperature. The phase transition temperature depends on the vesicle size in a sigmoidal fashion. Throughout the entire 200-700 A diamter range, the phase transition parameters are sensitive to size; however, the size dependence is especially pronounced around 400 A in diameter. The anomalous size dependence of the transition temperature for vesicles smaller than 400 A in diameter has been attributed to a decrease in the effective bilayer curvature due to packing rearrangements of the lipid molecules. Changes in the fractional degree of self-quenching of trapped 6-carboxyfluorescein induced by osmotic stress indicate that large single lamellar vesicles are not spherical under isoosmotic conditions. These vesicles are relatively flexible and can sustain almost a 2-fold increase in their internal aqueous volume without any leakage of the internal content.

Drug Stability↗
PubMed1981

Transbilayer distribution of phosphatidylethanolamine in large and small unilamellar vesicles.

There is much evidence which strongly suggests that most constituents of biological membranes display a transbilayer compositional asymmetry. The tendency of binary mixtures of phospholipids to form compositionally asymmetric bilayers spontaneously has been studied extensively. In small unilamellar vesicles, most mixtures of phospholipids with different head groups have been reported to be nonrandomly arranged across the bilayer. In this study, the influence of the radius of curvature on the transbilayer phospholipid distribution has been investigated. The distribution of egg phosphatidylethanolamine in large unilamellar vesicles comprised of egg phosphatidylethanolamine and egg was determined by 2,4,6-trinitrobenzenesulfonic acid labeling. These large vesicles were obtained by modifying the ethanol injection procedure originally described by Batzri & Korn (1973) [Batzri, S., & Korn, E. D. (1973) Biochim. Biophys. Acta 298, 1015] by using a slow injection rate. After injection, the ethanol was removed by molecular sieve chromatography and the vesicle dispersion centrifuged. This results in a population of large, homogeneous, and unilamellar vesicles as determined by molecular sieve chromatography, 32P NMR, and electron microscopy. The phosphatidylethanolamine component in unilamellar vesicles of this type is equally distributed between the two monolayers. In contrast, phosphatidylethanolamine in small unilamellar vesicles is known to be preferentially localized in the outer monolayer at low phosphatidylethanolamine concentrations and in the inner monolayer at high phosphatidylethanolamine concentrations. These results suggest that while phospholipids may form asymmetric bilayers spontaneously in highly curved regions of biological membranes, other factors must be responsible for the generalized phospholipid asymmetry seen in these systems.

Egg Yolk↗
PubMed1980

Fusion of dipalmitoylphosphatidylcholine vesicles.

Small unilamellar dipalmitoylphosphatidylcholine vesicles formed by sonication are shown to fuse spontaneously below the phase transition temperature. The ultimate fusion products are unilamellar vesicles about 700 A in diameter, which are stable and provide an intact ionic permeation barrier either above or below the phase transition. The fused vesicles have been characterized by gel chromatography, trapped volume, 31P nuclear magnetic resonance, and negative stain and freeze-fracture electron microscopy.

Chromatography, Gel↗