924 research outputs found
Analysing protein competition on self-assembled mono-layers studied with quartz crystal microbalance
The mechanisms by which proteins adsorb to surfaces of biomaterials have long been of interest. The
present work started with the premise that small/hard and large/soft proteins will yield different sets
of normalized frequency shift and dissipation signals when studied with a quartz crystal microbalance.
The aim was to evaluate the usefulness of these raw data to study protein competition using protein incubations
in sequence and from mixtures of albumin (BSA) and gamma-globulin (BGG) at various ratios.
Increasing the concentration of BSA decreases the adsorption of subsequently incubated BGG. For BSA/
BGG mixtures the dissipation is similar for all logarithmic molar ratios BGG/BSA below 1 but soon
decreases when the molar ratio of BSA/BGG (and opposite for the normalized frequency shift) is above
1, indicating preferential binding of BGG. Modelling indicated that differences in the film shear modulus
and viscosity depend more on the properties of the self-assembling mono-layers (SAMs) than on the proteins.
Films high in BSA tentatively differ in film shear modulus and viscosity from that of films high in
BGG but only on the hydrophobic surfaces. The results were encouraging as the raw data were deemed to
be able to point at protein adsorption competition.The authors thank the Portuguese National Science and Technology Foundation (FCT) for the Project Grants PTDC/FIS/68517/2006 and PTDC/FIS/68209/2006, and personal Grant BPD/39331/2007 for J.B
Recommendations for reporting ion mobility Mass Spectrometry measurements
Here we present a guide to ion mobility mass spectrometry experiments, which covers both linear and nonlinear methods: what is measured, how the measurements are done, and how to report the results, including the uncertainties of mobility and collision cross section values. The guide aims to clarify some possibly confusing concepts, and the reporting recommendations should help researchers, authors and reviewers to contribute comprehensive reports, so that the ion mobility data can be reused more confidently. Starting from the concept of the definition of the measurand, we emphasize that (i) mobility values (K0) depend intrinsically on ion structure, the nature of the bath gas, temperature, and E/N; (ii) ion mobility does not measure molecular surfaces directly, but collision cross section (CCS) values are derived from mobility values using a physical model; (iii) methods relying on calibration are empirical (and thus may provide methodâdependent results) only if the gas nature, temperature or E/N cannot match those of the primary method. Our analysis highlights the urgency of a community effort toward establishing primary standards and reference materials for ion mobility, and provides recommendations to do so. © 2019 The Authors. Mass Spectrometry Reviews Published by Wiley Periodicals, Inc
Fluorescence probe techniques to monitor protein adsorption-induced conformation changes on biodegradable polymers
The study of protein adsorption and any associated conformational changes on interaction with biomaterials is of great importance in the area of implants and tissue constructs. This study aimed to evaluate some fluorescent techniques to probe protein conformation on a selection of biodegradable polymers currently under investigation for biomedical applications. Because of the fluorescence emanating from the polymers, the use of monitoring intrinsic protein fluorescence was precluded. A highly solvatochromic fluorescent dye, Nile red, and a well-known protein label, fluorescein isothiocyanate, were employed to study the adsorption of serum albumin to polycaprolactone and to some extent also to two starch-containing polymer blends (SPCL and SEVA-C). A variety of fluorescence techniques, steady state, time resolved, and imaging were employed. Nile red was found to leach from the protein, while fluorescein isothiocyanate proved useful in elucidating a conformational change in the protein and the observation of protein aggregates adsorbed to the polymer surface. These effects were seen by making use of the phenomenon of energy migration between the fluorescent tags to monitor interprobe distance and the use of fluorescence lifetime imaging to ascertain the surface packing of the protein on polymer
Morphology and miscibility of chitosan/soy protein blended membranes
A physico-chemical characterization of blended membranes composed by chitosan and soy protein has been carried out in order to
probe the interactions that allow membranes to be formed from these biopolymer mixtures. These membranes are developed aiming at
applications in wound healing and skin tissue engineering scaffolding. The structural features of chitosan/soy blended membranes were
investigated by means of solid state carbon nuclear magnetic resonance (NMR), infrared spectroscopy (FTIR), contact angle, and atomic
force microscopy. FTIR investigations suggested that chitosan and soy may have participated in a specific intermolecular interaction.
The proton spinâlattice relaxation experiments in the rotating frame on blended membranes indicated that independently of the preparation
conditions, the blend components are not completely miscible possibly due to a weak polymerâprotein interaction. It was also
shown that the blended systems showed a rougher surface morphology which was dependent of soy content in the blend system
Hybrid biodegradable membranes of silane-treated chitosan/soy protein for biomedical applications
In recent years, progress in the field of hybrid materials has been accelerated through use of the solâgel process for creating materials and devices, which benefit from the incorporation of both inorganic and organic components. In this work, organicâinorganic hybrid membranes were prepared from tetraethoxysilane and a blend system composed of chitosan and soy protein. By introducing a small amount of siloxane bond into the chitosan/soy protein system, the chitosan/soy protein hybrid membranes were improved in terms of structure, topography and mechanical properties. It appears that the chitosan/soy protein hybrid membranes were formed by discrete inorganic moieties entrapped in the chitosan/soy protein blend, which improved the stability and mechanical performance assessed by the dynamic mechanical analysis as compared to chitosan/soy protein membrane. Also, in vitro cell culture studies evidenced that the chitosan/soy protein hybrid membranes are non-cytotoxic over a mouse fibroblast-like cell line. The hybrid membranes of silane-treated chitosan/soy protein developed in this work have potential in biomedical applications, including tissue engineering.This work was financially supported by the Portuguese Foundation for Science and Technology - FCT (Grant SFRH/BPD/45307/2008, SFRH/BPD/21786/2009, SFRH/BPD/39331/2007 and SFRH/BD/64601/2009), 'Fundo Social Europeu' - FSE and 'Programa Diferencial de Potencial Humano - POPH' and was partially supported by the FEDER through POCTEP 0330_IBEROMARE_1_P
Application of fluorescence techniques to the study of protein adsorption and packing on biomaterial surfaces
[Excerpt] The ways proteins compete for the surface of biomaterials and
change conformation are believed to be important for the host response
to implants. It is possible to elucidate information on
packing and any induced conformational change by making use of
different fluorescence techniques on fluorescently labelled proteins.
Employing probe-probe resonance energy transfer (RET) allows
inter and intra protein interactions to be distinguished. Homo resonance
energy transfer (hRET) avoids many problems with having
two different probes and means that labelling and subsequent purification
can be done in one step. [...]Portuguese Foundation for Science and
Technology, project PROTEOLIGHT (PTDC/FIS/68517/2006)
and J.B. grant SFRH/BPD/17584/2004. European Union NoE
EXPERTISSUES (NMP3-CT-2004-500283) and European Union
FP6 STREP project HIPPOCRATES (NMP3-CT-2003-505758).info:eu-repo/semantics/publishedVersio
Hsp70 oligomerization is mediated by an interaction between the interdomain linker and the substrate-binding domain
Oligomerization in the heat shock protein (Hsp) 70 family has been extensively documented both in vitro and in vivo, although the mechanism, the identity of the specific protein regions involved and the physiological relevance of this process are still unclear. We have studied the oligomeric properties of a series of human Hsp70 variants by means of nanoelectrospray ionization mass spectrometry, optical spectroscopy and quantitative size exclusion chromatography. Our results show that Hsp70 oligomerization takes place through a specific interaction between the interdomain linker of one molecule and the substrate-binding domain of a different molecule, generating dimers and higher-order oligomers. We have found that substrate binding shifts the oligomerization equilibrium towards the accumulation of functional monomeric protein, probably by sequestering the helical lid sub-domain needed to stabilize the chaperone: substrate complex. Taken together, these findings suggest a possible role of chaperone oligomerization as a mechanism for regulating the availability of the active monomeric form of the chaperone and for the control of substrate binding and release
Space Charge Study of the Jefferson Lab Magnetized Electron Beam
Magnetized electron cooling could result in high luminosity at the proposed Jefferson Lab Electron-Ion Collider (JLEIC). In order to increase the cooling efficiency, a bunched electron beam with high bunch charge and high repetition rate is required. We generated magnetized electron beams with high bunch charge using a new compact DC high voltage photo-gun biased at -300 kV with alkali-antimonide photocathode and a commercial ultrafast laser. This contribution explores how magnetization affects space charge dominated beams as a function of magnetic field strength, gun high voltage, laser pulse width, and laser spot size
Surface engineered carboxymethylchitosan/poly(amidoamine) dendrimer nanoparticles for intracellular targeting
Novel highly branched biodegradable macromolecular systems have been developed by grafting carboxymethylchitosan
(CMCht) onto low generation poly(amidoamine) (PAMAM) dendrimers. Such structures organize into sphere-like nanoparticles
that are proposed to be used as carriers to deliver bioactive molecules aimed at controlling the behavior of stem cells,
namely their proliferation and differentiation. The nanoparticles did not exhibit significant cytotoxicity in the range of
concentrations below 1 mg mL"1, and fluorescent probe labeled nanoparticles were found to be internalized with highly
efficiency by both human osteoblast-like cells and rat bone marrow stromal cells, under fluorescence-activated cell sorting and
fluorescence microscopy analyses. Dexamethasone (Dex) has been incorporated into CMCht/PAMAM dendrimer nanoparticles
and release rates were determined by high performance liquid chromatography. Moreover, the biochemical data demonstrates
that the Dex-loaded CMCht/PAMAM dendrimer nanoparticles promote the osteogenic differentiation of rat bone marrow
stromal cells, in vitro. The nanoparticles exhibit interesting physicochemical and biological properties and have great potential to
be used in fundamental cell biology studies as well as in a variety of biomedical applications, including tissue engineering and
regenerative medicine
PEPPo: Using a Polarized Electron Beam to Produce Polarized Positrons
An experiment demonstrating a new method for producing polarized positrons has been performed at the CEBAF accelerator at Jefferson Laboratory. The PEPPo (Polarized Electrons for Polarized Positrons) concept relies on the production of polarized e+/eâ pairs originating from the bremsstrahlung radiation of a longitudinally polarized electron beam interacting within a 1.0 mm tungsten pair-production target. This paper describes preliminary results of measurements using an 8.2 MeV/c electron beam with polarization 84% to generate positrons in the range of 3.1 to 6.2 MeV/c with polarization as high as âŒ80%
- âŠ