排序方式: 共有29条查询结果,搜索用时 15 毫秒
1.
Pradier CM Rubio C Poleunis C Bertrand P Marcus P Compère C 《The journal of physical chemistry. B》2005,109(19):9540-9549
Adhesion of bacterial strains on solid substrates is likely related to the properties of the outer shell of the micro-organisms. Aiming at a better understanding and control of the biofilm formation in seawater, the surface chemical composition of three marine bacterial strains was investigated by combining Fourier transform IR spectroscopy, X-ray photoelectron spectroscopy (XPS), and time-of-flight secondary-ion mass spectrometry (ToF-SIMS). The D41 strain surface showed evidence of proteins, as deduced from the NH2 and NCO XPS and ToF-SIMS fingerprints; this strain was found to adhere to stainless steel, glass, or Teflon surfaces in a much higher quantity (2 orders of magnitude) than the two other ones, DA and D01. The latter are either enriched in COOH or sulfates, and this makes them more hydrophilic and less adherent to all substrates. Correlations with physicochemical properties and adhesion seem to demonstrate the role of the external layer composition, in particular the role of proteins more than that of hydrophobicity, on their adhesion abilities. 相似文献
2.
Yam CM Pradier CM Salmain M Fischer-Durand N Jaouen G 《Journal of colloid and interface science》2002,245(1):204-207
Fourier transform infrared reflection-absorption spectroscopy (FT-IRRAS) was successively used to monitor the covalent immobilization of biotin molecules onto a planar gold substrate covered with a self-assembled monolayer of cystamine and to transduce the molecular recognition of avidin and biotin. This detection was greatly facilitated and made selective by the labeling of avidin and of biotin with various transition metal carbonyl probes. The binding of avidin to the surface was optimized by blocking the nonspecific binding sites by adsorption of an unrelated protein, bovine serum albumin. This work exemplifies the feasibility of detecting biomolecular associations involving molecules of any size at a liquid/solid interface by using a simple and accessible surface analysis technique. 相似文献
3.
Humblot V Méthivier C Pradier CM 《Langmuir : the ACS journal of surfaces and colloids》2006,22(7):3089-3096
The adsorption of L-lysine on a Cu(110) surface has been investigated under UHV conditions from the sublimation of a crystalline phase. The adsorption was characterized by Fourier transform reflection absorption infrared spectroscopy (FT-RAIRS) during exposure and Auger electron spectroscopy (AES). At room temperature, the lysine molecules' adsorption geometry varies as a function of the exposure. At low coverage, the molecules are adsorbed via the oxygen atoms of the deprotonated carboxylate group and the nitrogen atom of the amino group. At high coverage, close to the monolayer, the molecules reorient to be anchored to the surface via one oxygen of a sideways-tilted carboxylate moiety. This first step is followed by the growth of multilayers of nonoriented molecules. In contrast, adsorption on an oxygen-modified copper surface leads to a rather disordered layer. The results are compared with the adsorption carried out on a polycrystalline copper surface after immersion in solutions of lysine at various pH values. The adsorption was monitored by polarization modulation infrared spectroscopy (PM-IRRAS). The chemistry of the adsorbed molecules is function of the starting chemical form of the lysine molecules imposed by the pH of the solution. The combination of the two techniques and various sets of adsorption conditions will give important insight into the adsorption of biomolecules on metal surfaces and the influence of water and surface oxygen. 相似文献
4.
This work is focused on studying the grafting of gold nanoparticles (Np) on a cystamine self-assembled monolayer on gold, in order to build sensitive immunosensors. The synthesis and deposition of gold nanoparticles, 13 and 55 nm sizes, were characterised by combining Polarisation Modulation Infrared Reflection-Absorption Spectroscopy (PM-IRRAS), X-ray Photoelectron Spectroscopy (XPS) Surface Enhanced Raman Scattering (SERS), and Atomic Force Microscopy (AFM) which all indicated the formation of a dispersed layer of nanoparticles. This observation is explained by the compromise between the high reactivity of amine-terminated layers towards gold, and interparticle repulsions. Nps were then functionalised with antibody probes, and the recognition by an anti-rIgG was assayed both on planar and Np gold surfaces.The important result is that nanoparticles of 55 nm are preferable for the following reasons: they enable to build a denser and well dispersed layer and they increase both the number of receptors (IgGs) and their accessibility. Beside these geometric improvements, a net enhancement of the Raman signal was observed on the 55 nm nanoparticle layer, making this new platform promising for optical detection based biosensors. 相似文献
5.
Souhir Boujday Romain Briandet Michèle Salmain Jean-Marie Herry Pierre-Guy Marnet Michel Gautier Claire-Marie Pradier 《Mikrochimica acta》2008,163(3-4):203-209
We describe the elaboration of ultra-sensitive immunosensors, to detect the bacterial pathogen Staphylococcus aureus. We utilized commercially available polyclonal anti-S. aureus antibody as receptor. Immunosensors were elaborated by building a self-assembled monolayer (SAM) of thiolamine onto planar gold-coated sensor chips. Then, Protein A was covalently linked to the thiolated SAM using glutaraldehyde as cross-linking agent. After a blocking step by Bovine Serum Albumin (BSA), the antibody was immobilized by affinity to Protein A. This step-by-step construction was monitored by Polarization Modulation Reflection Absorption Infrared Spectroscopy (PM-RAIRS) and Quartz Crystal Microbalance with Dissipation (QCM-D). In a first stage, the parameters of immunosensor elaboration were optimized using a model rabbit IgG. The accessibility of receptors and the homogeneity of their distribution were checked by PM-RAIRS, QCM-D, and by immuno-gold scanning electron microscopy. Then, the specific rabbit anti-S. aureus antibody was immobilized and the resulting sensing layer was applied to the detection of the pathogen target. Independent detection of bacteria immobilized on the sensors by fluorescent imaging allowed validation of the specificity of recognition toward the pathogen as well as a quantitative response of the sensor. Using PM-RAIRS as transducing technique allowed us to enhance sensitivity and reach a very competitive detection level (105 CFU mL?1). 相似文献
6.
Binary mixtures of 11-mercaptoundecanoic acid (MUA) and other thiols of various lengths and terminal functions were chemisorbed on gold-coated surfaces via S–Au bonds to form mixed self-assembled monolayers (SAMs). Several values of the mole fraction of MUA in the thiol mixtures were tested and the structure and composition of the resulted thin films were characterized by X-ray photoelectron spectroscopy (XPS) and polarization modulation infrared reflection-absorption spectroscopy (PM-IRRAS). The results made it clear that co-adsorption of MUA with thiols of similar chain length led to well-ordered monolayers whereas the co-adsorption of MUA with shorter thiols yielded less crystalline-like thin films, but with more reactive carboxylic acid terminal groups. This criterion appeared decisive for efficient covalent binding of Staphylococcus aureus Protein A (PrA), a protein that displays high affinity for the constant fragment (Fc) of antibodies of the IgG type from various mammal species. The ability of immobilized Protein A to recognize and bind a model IgG appeared to be optimal for the mixed SAM of MUA and the short-chain, ω-hydroxythiol 6-mercaptohexanol in the proportion 1–3. 相似文献
7.
Erin E. Bedford Jolanda Spadavecchia Claire‐Marie Pradier Frank X. Gu 《Macromolecular bioscience》2012,12(6):724-739
SPR biosensing is increasingly popular for the detection of a multitude of biomolecules. It offers label‐free detection and study of proteins, nucleic acids, and other biomolecules in real time. A recent trend involves incorporation of AuNPs, either within the sensing surface itself or as signal enhancing tagging molecules. The importance of AuNP and detecting agent spacing is described and techniques using macromolecular spacing aids are highlighted. Recent methods to enhance SPR detection capabilities using gold nanoparticles are reviewed, as well as device fabrication and the results of incorporation. SPR detection is a highly versatile method for the detection of biomolecules and, with the incorporation of AuNPs, shows promise in extending it to a number of new applications.
8.
Chi-Ming Yam Liu Zheng Michle Salmain Claire-Marie Pradier Philippe Marcus Grard Jaouen 《Colloids and surfaces. B, Biointerfaces》2001,21(4)
We compare herein the interfacial reactivity of self-assembled monolayers (SAMs) of 11-mercaptoundecanoic acid (MUA), 1-undecanethiol (UDT) and 11-mercaptoundecanol (MUD) on gold surfaces towards aqueous solutions of poly-(
-lysine) (PL). Liquid-phase labelling of PL with the alkyne dicobalt hexacarbonyl cluster 1 combined with analysis of the substrates by Fourier transform infrared reflection–absorption spectroscopy (FT-IRRAS) and X-ray photoelectron spectroscopy (XPS) revealed that irreversible binding of PL occurred in all cases. However, the mechanism of binding involved differed markedly from one monolayer to the other. The main mode of interaction of PL to MUA SAM was of electrostatic nature between the terminal carboxylate of MUA and the ammonium groups of PL. For a similar number of bound thiolate molecules, the UDT adsorbed layer was found less continuous than the MUA one, allowing a higher fraction of PL to directly bind to the gold surface. As for MUD, very little thiolate molecules were adsorbed, leaving bare gold surface areas for non specific adsorption of PL. 相似文献
9.
Simon Clavaguera Olivier J. Dautel Lionel Hairault Christophe Méthivier Pierre Montméat Eric Pasquinet Claire‐Marie Pradier Françoise Serein‐Spirau Salem Wakim Florian Veignal Joël J. E. Moreau Jean‐Pierre Lère‐Porte 《Journal of polymer science. Part A, Polymer chemistry》2009,47(16):4141-4149
The detection of 2,4‐dinitrotoluene (DNT) by fluorescence quenching of a new class of polyimines consisting in π‐conjugated segments regularly alternated with chiral C2 symmetry units has been studied for solutions and thin films. Their photophysical properties and their sensitivity towards DNT detection has been compared to those of a small model molecule incorporating the same π‐conjugated segment. In solution, all the compounds exhibit the same photo‐physical properties and sensitivity towards DNT detection. In contrast, for thin films, better performances are observed in static conditions for this new class of polyimines compared to the small model molecule. It seems that C2 symmetry units prevent from the stacking of the π‐conjugated segments and provide in addition to high fluorescence signal an improved diffusion of the analyte inside the films. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 4141–4149, 2009 相似文献
10.
Pradier CM Humblot V Stievano L Méthivier C Lambert JF 《Langmuir : the ACS journal of surfaces and colloids》2007,23(5):2463-2471
The adsorption of proteins is the first process to take place when a solid is immersed in a biological fluid; though not yet thoroughly understood at a molecular level, this process is also known to be strongly influenced by the presence of salt in solution or by pH changes. In the present work, poly-L-glutamic acid (PG) and poly-L-lysine (PL) were selected to mimic the behavior of some protein fragments. Their adsorption was investigated by infrared spectroscopy in various modes, both on planar and on divided (powder) surfaces of aluminum oxide. These two peptides were shown to have different behaviors when adsorbed from solutions with or without CaCl2 and at various pH values. Polarization modulation-reflection absorption infrared spectroscopy, applied in a special cell designed to characterize the solid surface in contact with the liquid, enabled the observation of the influence of pH and salts upon polypeptide adsorption. At pH values higher than 5 and in the presence of CaCl2 in solution, a net increase of the PG adsorbed amount is observed, whereas no such effect could be detected for PL. Specific interactions between the COO- groups on the side chains and the surface, or between those of two different molecules, was inferred. Interestingly, similar conclusions could be drawn for the surface of alumina powders contacted with solutions of PG and PL and characterized by attenuated total reflectance IR. This work demonstrates the potential for IR investigations of solid oxide-liquid interfaces combining the study of planar and finely divided surfaces. 相似文献