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1.
Tapping-mode atomic force microscopy was used to study the time-dependent changes in the structure of fibrinogen under aqueous conditions following adsorption on two model surfaces: hydrophobic graphite and hydrophilic mica. Fibrinogen was observed in the characteristic trinodular form, and the dimensions of the adsorbed molecules were consistent with previously reported values for these surfaces. On the basis of the differences in the relative heights of the D and the E domains, four orientation states were observed for fibrinogen adsorbed on both the surfaces. On graphite, the initial asymmetric orientation states disappeared with spreading over time. Some small lateral movements of the adsorbed proteins were observed on mica during repeated scanning, whereas no such movement was observed on graphite, indicating strong adhesion of fibrinogen to a hydrophobic surface. Spreading kinetics of fibrinogen on the two surfaces was determined by measuring the heights of the D and E domains over a time period of approximately 2 h. On graphite, the heights of both the D and E domains decreased with time to a lower plateau value of 1.0 nm. On mica, the heights of both the D and E domains showed an increase, rising to an upper plateau value of approximately 2.1 nm. The spreading of the D and E domains on graphite was analyzed using an 'exponential-decay-of-height' model. A spreading rate constant of approximately 4.7 x 10(-4) s(-1) was observed for the whole fibrinogen molecule adsorbed on graphite, corresponding to a free energy of unfolding of approximately 37 kT. Extrapolation of the exponential curve in the model to t = 0 yielded values of 2.3 and 2.2 nm for the heights of the D and the E domains at the time of contact with the hydrophobic graphite substrate, significantly less than their free solution diameters. A two-step spreading model is proposed to explain this observation. 相似文献
2.
The adsorption and micellar behavior of diethylene glycol mono-n-tetradecyl ether (C14E2), sodium 3,6,9,12-tetraoxaoctacosanoate (TOOCNa), and their mixture at a 1:1 molar ratio have been studied by film balance, Brewster angle microscopy (BAM), and surface tensiometry at different temperatures. The monolayers of pure C14E2 and its mixture with TOOCNa show a first-order phase transition with a conspicuous cusp point in their respective adsorption isotherms. This is further confirmed by the observation of bright two-dimensional condensed phase domains visualized by BAM just after the appearance of the phase transition. It is interesting to note here that for C14E2, condensed domains are observed up to 19 degrees C, while in the mixed system, they are observed up to 22 degrees C. To understand why in the mixed system the domains are observed at higher temperatures than for pure C14E2, we have measured the temperature dependency of the equilibrium surface tension at > or = cmc (gammacmc) values of both the pure and the mixed systems. The gammacmc values of pure C14E2 remain almost constant, while those of pure TOOCNa and its mixture with C14E2 decrease appreciably with increasing temperature. It is concluded that higher degree of dehydration of the ethylene oxide (EO) chain reduces the head-group size of TOOCNa, which outweighs the combined effect of the repulsive interactions between the head-groups and the thermal motion of the adsorbed molecules. Furthermore, C14E2 being inserted into the TOOCNa monolayer reduces the electrostatic repulsions between the charged heads, and consequently, the adsorbed monolayers attain closer molecular packing. As a result, the gammacmc values of both pure TOOCNa and its mixture with C14E2 decrease with increasing temperature. This facilitates the formation of condensed domains in the mixed system at higher temperatures, whereas none of the individual members can show any indicative feature of phase transition under the same experimental conditions. 相似文献
3.
We present the adsorption kinetics and surface morphology of the adsorbed monolayers of bis(ethylene glycol) mono-n-tetradecyl ether (C14E2) by film balance and Brewster angle microscopy. A cusp point followed by a plateau region in the pressure (pi)-time (t) adsorption isotherm indicates a first-order phase transition in the coexistence region between a lower density liquid expanded (LE) phase and a higher density liquid condensed (LC) phase. A variety of condensed phase domains surrounded by the homogeneous LE phase are observed just after the appearance of the phase transition. The domains are of a spiral or striplike structure at lower temperatures. This characteristic shape of the domains is because of strong dipole-dipole repulsion between the molecules. At 18 degrees C, the domains are found to be quadrant structures. A slight increase in subphase temperature (around 1 degrees C) brings about a quadrant-to-circular shape transition in the domains. The circular domains return to quadrant structures as the subphase temperature is lowered. The domains completely disappear when the temperature is increased beyond 19 degrees C, suggesting that the critical temperature for the condensed domain formation is 19 degrees C. Above this temperature, the hypothetical surface pressure necessary for the phase transition exceeds the actual surface pressure attainable from a solution of concentration greater than or equal to the critical micelle concentration. An increase in molecular motion with increasing temperature results in a higher degree of chain flexibility. As a result, the molecules cannot accumulate in the condensed phase form when the subphase temperature is above 19 degrees C. 相似文献
4.
Weiss VC 《The Journal of chemical physics》2006,125(8):084718
The wetting behavior of alkanes of medium chain length (e.g., pentane, hexane, and heptane) on water is more complex than the usually observed first-order wetting transition from partial to complete wetting by showing a sequence of two transitions. In this sequential-wetting scenario, a first-order transition from a microscopically thin to a mesoscopically thick layer of liquid on the substrate surface is followed by a continuous divergence of the film thickness upon increase of the temperature. This critical transition to complete wetting at T(w,c) is solely determined by long-range interactions between substrate and adsorbate, which are well-described by Dzyaloshinskii-Lifshitz-Pitaevskii [Adv. Phys. 10, 165 (1961)] theory in terms of the static dielectric constants and the refractive indices of the media involved. The first-order thin-thick transition, however, which occurs at a lower temperature T(w,1), results from an interplay of short-range and long-range forces and is notoriously more difficult to describe because a satisfactory theory of the short-range interactions between substrate and adsorbate is still missing. The approach presented in this paper attempts to account for the short-range interactions in an effective way: Within a Cahn-type [J. Chem. Phys. 66, 3667 (1977)] theory that has been augmented for long-range interactions and modified to treat the first layer of adsorbed molecules in a lattice-gas approach, the contact energy is deduced from the surface pressure, which in turn is calculated using a two-dimensional van der Waals equation of state and an expression for the Henry's law constant that was derived by Hirasaki [J. Adhes. Sci. Technol. 7, 285 (1993)]. The method uses only the dielectric properties of the isolated bulk media and simple assumptions on the size and the shape of the adsorbed alkane molecules and leads to satisfactory results for the transition temperatures T(w,1) and T(w,c). 相似文献
5.
Blom A Warr GG Wanless EJ 《Langmuir : the ACS journal of surfaces and colloids》2005,21(25):11850-11855
The structure of adsorbed layers of several polyoxyethylene alkyl ether (C(n)E(m)) nonionic surfactants on silica and graphite surfaces has been imaged using atomic force microscopy as a function of temperature up to their cloud points. For all surfactants with a cloud point within the experimentally accessible range, the adsorbed layer morphology on silica evolved from globules at low temperatures first into rods and then a mesh with increasing temperature. This mesh structure was retained even when the solutions were heated above their cloud points into the two-phase coexistence region. Only C(12)E(3) was observed to form a laterally unstructured bilayer. On graphite, all surfactants formed straight, parallel hemicylinders at all temperatures examined. 相似文献
6.
The reactions of tetrakis(dimethylamido)titanium, Ti[N(CH(3))(2)](4), with alkyltrichlorosilane self-assembled monolayers (SAMs) terminated by -OH, -NH(2), and -CH(3) groups have been investigated with X-ray photoelectron spectroscopy (XPS). For comparison, a chemically oxidized Si surface, which serves as the starting point for formation of the SAMs, has also been investigated. In this work, we examined the kinetics of adsorption, the spatial extent, and stoichiometry of the reaction. Chemically oxidized Si has been found to be the most reactive surface examined here, followed by the -OH, -NH(2), and -CH(3) terminated SAMs, in that order. On all surfaces, the reaction of Ti[N(CH(3))(2)](4) was relatively facile, as evidenced by a rather weak dependence of the initial reaction probability on substrate temperature (T(s) = -50 to 110 degrees C), and adsorption could be described by first-order Langmuirian kinetics. The use of angle-resolved XPS demonstrated clearly that the anomalous reactivity of the -CH(3) terminated SAM could be attributed to reaction of Ti[N(CH(3))(2)](4) at the SAM/SiO(2) interface. Reaction on the -NH(2) terminated SAM proved to be the "cleanest", where essentially all of the reactivity could be associated with the terminal amine group. In this case, we found that approximately one Ti[N(CH(3))(2)](4) adsorbed per two SAM molecules. On all surfaces, there was significant loss of the N(CH(3))(2) ligand, particularly at high substrate temperatures, T(s) = 110 degrees C. These results show for the first time that it is possible to attach a transition metal coordination complex from the vapor phase to a surface with an appropriately functionalized self-assembled monolayer. 相似文献
7.
Gu YS Decker EA McClements DJ 《Langmuir : the ACS journal of surfaces and colloids》2006,22(18):7480-7486
The influence of isothermal heat treatments on the adsorption of anionic carrageenan molecules to the surfaces of anionic beta-lactoglobulin-coated droplets has been investigated. The zeta-potential, mean particle diameter, microstructure, and creaming stability of emulsions containing beta-lactoglobulin-coated droplets and/or carrageenan molecules that had previously been heat treated at temperatures ranging from 30 to 90 degrees C for 20 min were measured (pH 6.0, 150 mM NaCl). Three different heat treatments were used to establish the physicochemical origin of the influence of thermal history on the adsorption of carrageenan molecules to the protein coated droplets: (i) droplets and carrageenan were mixed at room temperature, then heated together; (ii) droplets were heated, cooled to room temperature, then mixed with carrageenan; (iii) carrageenan was heated, cooled to room temperature, then mixed with droplets. For treatments i and ii appreciably more carrageenan adsorbed to the protein-coated droplet surfaces at temperatures < or = 60 degrees C than at higher temperatures. For treatment iii, carrageenan adsorbed to the droplet surfaces across the whole temperature range. These results suggest that an irreversible thermal denaturation of the adsorbed beta-lactoglobulin molecules inhibited the adsorption of carrageenan molecules to the droplet surfaces. We postulate that there is a patch of positive charge on the surface of the native globular protein molecules which becomes more diffuse upon thermal denaturation. We found that the carrageenan molecules were unable to protect the beta-lactoglobulin-coated droplets at high temperatures (T > 60 degrees C) because they desorbed from the droplet surfaces. Nevertheless, adsorption of iota-carrageenan was capable of protecting the droplets against flocculation caused by surface denaturation of the adsorbed proteins at lower temperatures (T < or = 50 degrees C). 相似文献
8.
We present the adsorption kinetics and the surface phase behavior of water-soluble n-tetradecyl phosphate (n-TDP) at the air-water interface by film balance and Brewster angle microscopy (BAM). The relaxation of the surface pressure at about zero value in the surface pressure (pi)-time (t) adsorption isotherm is found to occur from 2 to 20 degrees C with appropriate concentrations of the amphiphile. These plateaus are accompanied by two surface phases, confirming that the relaxation of the surface pressure is caused by a first-order phase transition. Only this phase transition is observed at <6.5 degrees C and it is considered as a gas (G)-liquid condensed (LC) phase transition. Above 6.5 degrees C, the phase transition at zero surface pressure is followed by another phase transition, which is indicated by the presence of cusp points in the pi-t curves at different temperatures. Each of the cusp points is followed by a plateau, which is accompanied by two surface phases, indicating that the latter transitions are also first-order in nature. At >6.5 degrees C, the former transition is classified as a first-order G-liquid expanded (LE) phase transition, while the latter transition is grouped into a first-order LE-LC phase transition. The critical surface pressure (pi(c)) necessary for the G-LC and G-LE phase transitions is zero and remains constant all over the studied temperatures, whereas that for the LE-LC transition increases linearly with increasing temperature. Based on these results, we construct a rather elaborated phase diagram that shows that the triple point for Gibbs monolayers of n-TDP is 6.5 degrees C. All the results are consistent with the present understanding of the Langmuir monolayers of insoluble amphiphiles at the air-water interface. 相似文献
9.
We have studied the anchoring of the nematic liquid crystal 5CB (4'-n-pentyl-4-cyanobiphenyl) as a function of the surface wettability, thickness of the liquid crystal layer, and temperature by measuring the birefringence of a hybrid aligned nematic cell where the nematic material was confined between octadecyltriethoxysilane-treated glass surfaces, with one surface linearly varying in its hydrophobicity. A homeotropic-to-tilted anchoring transition was observed as a function of the lateral distance along the hydrophobicity gradient, typically in a region corresponding to a water contact angle of approximately 64 degrees. The effect of the nematic layer thickness was measured simultaneously by preparing a wedge cell where the thickness varied along the direction perpendicular to the wettability. The detailed behavior of the onset of birefringence was found to be consistent with a dual-easy-axis model that predicts a discontinuous anchoring transition from homeotropic to planar. The anchoring was independent of temperature, except within 1 degrees C of the nematic-to-isotropic transition temperature (T(NI)). As the temperature approached T(NI), the tendency for planar anchoring gradually increased relative to that for homeotropic anchoring. 相似文献
10.
The thermodynamic quantities associated to the transformation from graphite to multiwalled carbon nanotubes (MWCNTs) were determined by electromotive force (emf) and differential scanning calorimetry (DSC) measurements. From the emf versus T data of galvanic cell Mo|Cr(3)C(2), CrF2, MWCNTs|CaF2 s.c.|Cr(3)C(2), CrF2, graphite|Mo with CaF2 as solid electrolyte, Delta(r)H(T) degrees= 8.25 +/- 0.09 kJ mol(-1) and Delta(r)S(T) degrees= 11.72 +/- 0.09 JK(-1) mol(-1) were found at average temperature T = 874 K. The transformation enthalpy was also measured by DSC of the Mn(7)C(3) formation starting from graphite or MWCNTs. Thermodynamic values at 298 K were calculated to be: Delta(r)H(298) degrees = 9.0 +/- 0.8 kJ mol(-1) as averaged value from both techniques and Delta(r)S(298) degrees approximately Delta(r)S(T) degrees. At absolute zero, the residual entropy of MWCNTs was estimated 11.63 +/- 0.09 JK(-1) mol(-1), and transformation enthalpy Delta(r)H(0) degrees approximately Delta(r)H(298) degrees. The latter agrees satisfactorily with the theoretical calculations for the graphite-MWCNTs transformation. On thermodynamic basis, the transformation becomes spontaneous above 704 +/- 13 K. 相似文献
11.
The temperature-dependent surface phase behavior of two sparingly soluble surfactants, namely, ethylene glycol n-dodecyl ether (EGDE) and ethylene glycol n-tetradecyl ether (EGTE), at the air-water interface was investigated by film balance and Brewster angle microscopy (BAM). A cusp point followed by a pronounced plateau region in the surface pressure-time (pi-t) adsorption isotherms of the amphiphiles measured by film balance indicates the first-order phase transition. Bright two-dimensional condensed phase domains in a dark background are observed by BAM just after the phase transition. In both cases the critical surface pressure necessary for the phase transition increases with increasing temperature. The domains are found to be circular up to 5 and 27 degrees C for EGDE and EGTE, respectively, above which they show a fingering pattern. Condensed domains are observed up to 23 and 37 degrees C for EGDE and EGTE, respectively. The surface properties of the amphiphiles are found to be markedly affected by their tendency to aggregate in the bulk as micelles. The CMC values of both the amphiphiles show a maximum at a definite temperature, T(max), that corresponds well to their respective maximum temperatures of domain formation. An increase in temperature beyond T(max) results in an increasing trend for the formation of micelles. Consequently the system suffers from a shortage of two-dimensional surface concentration of the molecules to attain the surface pressure necessary for phase transition. With increasing temperature, the enthalpy, DeltaH(m) degrees , and entropy, DeltaS(m) degrees , of micellization change from negative to positive in both cases. An enthalpy-entropy compensation effect is found to hold for both the amphiphiles over the entire temperature range. The thermodynamic quantities reveal that the increase in temperature is favorable for micellization when the temperature exceeds the corresponding T(max) of the amphiphiles. 相似文献
12.
Adsorption of fibrinogen on tantalum oxide, titanium oxide and gold studied by the QCM-D technique 总被引:2,自引:0,他引:2
Hemmersam AG Foss M Chevallier J Besenbacher F 《Colloids and surfaces. B, Biointerfaces》2005,43(3-4):208-215
The adsorption of human fibrinogen on tantalum oxide, titanium oxide and gold surfaces has been studied by quartz crystal microbalance with dissipation (QCM-D) at 37 degrees C. Two different protein concentrations have been used, one close to physiological concentration (1 mg/ml) and one significantly lower (0.033 mg/ml). To further characterize the adsorbed fibrinogen layer, the subsequent binding of both polyclonal and monoclonal antibodies of fibrinogen is studied. We found that the viscoelastic properties of the fibrinogen layer depends strongly on the initial protein concentration. The trend is generally seen for all three surfaces. The fibrinogen layer on gold and tantalum oxide is found to have the same viscoelastic properties, which are different from those found for the fibrinogen layer adsorbed on titanium oxide. The dependency of the surface chemistry on the viscoelastic properties of the fibrinogen layer is observed directly for the 0.033 mg/ml solution, and indirectly through the antibody response for the 1 mg/ml solution. From this we conclude that the orientation and/or denaturation of fibrinogen on a surface depends on the surface chemistry and the protein concentration in the solution, and that the binding of antibodies is a useful way to detect this difference. 相似文献
13.
López-García JJ Horno J Grosse C Delgado AV Shilov VN 《Journal of colloid and interface science》2001,237(1):98-103
Electrostatic effects on protein adsorption were investigated using differential scanning calorimetry (DSC) and adsorption isotherms. The thermal denaturation of lysozyme, ribonuclease A (RNase), and alpha-lactalbumin in solution and adsorbed onto silica nanoparticles was examined at three concentrations of cations: 10 and 100 mM of sodium and 100 mM of sodium to which 10 mM of calcium was added. The parameters investigated were the denaturation enthalpy (DeltaH), the temperature at which the denaturation transition was half-completed (T(m)), and the temperature range of the denaturation transition. For lysozyme and RNase, adsorption isotherms depend strongly on the ionic strength. At low ionic strength both proteins have a high affinity for the silica particles and adsorption is accompanied by a 15-25% reduction in DeltaH and a 3-6 degrees C decrease in T(m), indicating that the adsorbed state of the proteins is destabilized. Also, an increase in the width of the denaturation transition is observed, signifying a larger conformational heterogeneity of the surface bound proteins. At higher ionic strengths, both with and without the addition of calcium, no significant adsorption-induced alteration in DeltaH was observed for all three proteins. The addition of calcium, however, decreases the width of the denaturation transition for lysozyme and RNase in the adsorbed state. Copyright 2001 Academic Press. 相似文献
14.
Surfaces with resistance to non-specific protein adsorption and a high capacity to bind plasminogen from plasma are developed for application as fibrinolytic surfaces in blood contact. A new method is reported for grafting poly(OEGMA-co-HEMA) copolymers on polyurethane surfaces. The OEGMA provides effective protein resistance due to the PEG side chains and the HEMA provides a high density of OH groups for attachment of lysine. Adsorption of fibrinogen from buffer and plasma to these surfaces is low, indicating significant protein resistance. Plasminogen binding from plasma is high, and clot dissolution on surfaces where plasminogen adsorbed from plasma is converted to plasmin is rapid. 相似文献
15.
The long-term capacity-time dependence of 1-decanol was measured at the mercury/electrolyte interface for the electrolytes KCl, NaCl, LiBr, and K(2)SO(4), each of concentration 0.1 M, in the temperature range 20 to 50 degrees C and at 35 degrees C for electrolyte concentrations of NaCl in the region 0.05 to 0.4 M. All capacity-time dependences exhibited a slow increase of the capacity after a sudden decrease in the short-term range. The corresponding long-term time dependence of the degree of coverage can be theoretically well described with a first-order surface reaction. The ratios of final equilibrium capacity to minimal capacity can be explained with the formation of hemispherical or bilayer surface micelles from an initial monolayer of perpendicularly adsorbed molecules. A generalized packing parameter that involves the increase or decrease of the head groups' distance due to electrolyte ions or other surfactants was introduced. In the case of bilayers of parallel adsorbed molecules, obviously a new type of transition, which will be discussed in detail, occurs. 相似文献
16.
Frost RL Kristof J Horvath E Martens WN Kloprogge JT 《Journal of colloid and interface science》2002,251(2):350-359
Controlled rate thermal analysis (CRTA) allows the separation of adsorbed and intercalated hydrazine. CRTA displays the presence of three different types of hydrogen-bonded hydrazine in the intercalation complex: (a) The first is adsorbed loosely bonded on the kaolinite structure fully expanded by hydrazine-hydrate and liberated between approx 50 and 70 degrees C (b) The second intercalated hydrazine is lost between approx 70 and 85 degrees C. (c) The third type of intercalated-hydrazine molecule is lost in the 85-130 degrees C range. CRTA at 70 degrees C enables the removal of hydrazine-water and results in the partial collapse of the hydrazine-intercalated kaolinite structure to form a hydrazine-intercalated kaolinite. Removal of the adsorbed hydrazine enables the DRIFT spectra of the hydrazine-intercalated complex without any adsorbed hydrazine to be obtained. A band at 3626 cm(-1) attributed to the inner surface hydroxyls of kaolinite hydrogen bonded to hydrazine is observed. The intercalation of hydrazine-hydrate into kaolinite is complex and results from the different types of surface interactions of the hydrazine with the kaolinite surfaces. 相似文献
17.
Size dependence of second-order optical nonlinearity of CdS nanoparticles studied by hyper-Rayleigh scattering 总被引:2,自引:0,他引:2
Zhang Y Wang X Ma M Fu D Gu N Lu Z Xu J Xu L Chen K 《Journal of colloid and interface science》2003,267(2):377-381
Rutile TiO(2) particles were partly dissolved into aqueous solutions of H(2)SO(4), and the Ti(4+) ions were reprecipitated by adding NH(3) aq. Rutile-anatase coupled TiO(2) particles were prepared by heating the solid recovered after centrifugation of the suspension. The content of anatase (c(A), wt%) could be controlled arbitrarily by changing the dissolved amount of rutile. The photocatalytic activity for the gas-phase oxidation of acetaldehyde was evaluated. The first-order rate constant, k, strongly depended on both c(A) and heating temperature (T(c)), increasing with an increase in T(c) at T(c)=800 degrees C. The sample with c(A)=0.5 wt% prepared at T(c)=800 degrees C exhibited a much higher level of activity (k=0.94 h(-1)m(-2)) than those of pure rutile (k=0.08 h(-1)m(-2)) and anatase (k=0.34 h(-1)m(-2)). This remarkable enhancing effect was explained mainly in terms of photoinduced interfacial electron transfer from anatase to rutile. 相似文献
18.
The change in optical properties of colloidal gold upon aggregation has been used to develop an experimentally convenient colorimetric method to study the interfacial phase transition of an elastin-like polypeptide (ELP), a thermally responsive biopolymer. Gold nanoparticles, functionalized with a self-assembled monolayer (SAM) of mercaptoundecanoic acid onto which an ELP was adsorbed, exhibit a characteristic red color due to the surface plasmon resonance (SPR) of individual colloids. Raising the solution temperature from 10 degrees C to 40 degrees C thermally triggered the hydrophilic-to-hydrophobic phase transition of the adsorbed ELP resulting in formation of large aggregates due to interparticle hydrophobic interaction. Formation of large aggregates caused a change in color of the colloidal suspension from red to violet due to coupling of surface plasmons in aggregated colloids. The surface phase transition of the ELP was reversible, as seen from the reversible change in color upon cooling the suspension to 10 degrees C. The formation of colloidal aggregates due to the interfacial phase transition of adsorbed ELP was independently verified by dynamic light scattering of ELP-modified gold colloids as a function of temperature. Colloidal SPR provides a simple and convenient colorimetric method to study the influence of the solution environment, interfacial properties, and grafting method on the transition properties of ELPs and other environmentally responsive polymers at the solid-water interface. 相似文献
19.
Polarization-modulation infrared reflection-absorption spectroscopy (PM-IRRAS) was employed to investigate the interaction of serum protein fibrinogen with a biomedical-grade 316LVM stainless steel surface, in terms of the adsorption thermodynamics, kinetics and secondary structure changes of the protein. Apparent Gibbs energy of adsorption values indicated a highly spontaneous and strong adsorption of fibrinogen onto the surface. The kinetics of fibrinogen adsorption were successfully modeled using a pseudo first-order kinetic model. Deconvolution of the amide I bands indicated that the adsorption of fibrinogen on 316LVM results in significant changes in the protein's secondary structure that occur predominantly within the first minute of adsorption. Among the investigated structures, the alpha-helix structure undergoes the smallest changes, while the beta-sheet and beta-turns structures undergo significant changes. It was shown that lateral interactions between the adsorbed molecules do not play a role in controlling the secondary structure changes. An increase in temperature induced changes in the secondary structure of the protein, characterized by a loss of the alpha-helical content and its transformation into the beta-turns structure. 相似文献
20.
Bortolotti CA Battistuzzi G Borsari M Facci P Ranieri A Sola M 《Journal of the American Chemical Society》2006,128(16):5444-5451
Cyclic voltammetry experiments were carried out on native Saccharomyces cerevisiae iso-1-cytochrome c and its C102T/N62C variant immobilized on bare polycrystalline gold electrode through the S-Au bond formed by a surface cysteine. Experiments were carried out at different temperatures (5-65 degrees C) and pH values (1.5-7). The E degrees ' value at pH 7 (+370 mV vs SHE) is approximately 100 mV higher than that for the protein in solution. This difference is enthalpic in origin and is proposed to be the result of the electrostatic repulsion among the densely packed molecules onto the electrode surface. Two additional electrochemical waves are observed upon lowering the pH below 5 (E degrees ' = +182 mV) and 3 (E degrees ' = +71 mV), which are attributed to two conformers (referred to as "intermediate" and "acidic", respectively) featuring an altered heme axial ligation. This is the first determination of the reduction potential for low-pH conformers of cytochrome c in the absence of denaturants. Since the native form of cytochrome c can be restored, bringing back the pH to neutrality, the possibility offered by this transition to reversibly modulate the redox potential of cytochrome c is appealing for bioelectronic applications. The immobilized C102T/N62C variant, which differs from the native protein in the orientation of the heme group with respect to the electrode, shows very similar reduction thermodynamics. For both species, the rate constant for electron transfer between the heme and the electrode increases for the acidic conformer, which is also found to act as a biocatalytic interface for dioxygen reduction. 相似文献