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1.
Sci Rep ; 6: 36232, 2016 11 03.
Article in English | MEDLINE | ID: mdl-27808155

ABSTRACT

An oscillatory molecular adsorption pattern of the protein neutravidin from aqueous solution onto gold, in presence of a pre-deposited self assembled mono-molecular biotin film, is reported. Real time surface Plasmon resonance sensing was utilized for evaluation of the adsorption kinetics. Two different fractions were identified: in the initial phase, protein molecules attach irreversibly onto the Biotin ligands beneath towards the jamming limit, forming a neutravidin-biotin fraction. Afterwards, the growth rate exhibits distinct, albeit damped adsorption-desorption oscillations over an extended time span, assigned to a quasi reversibly bound fraction. These findings agree with, and firstly confirm a previously published model, proposing macro-molecular adsorption with time delay. The non-linear dynamic model is applicable to and also resembles non-damped oscillatory binding features of the hetero-catalytic oxidation of carbon monoxide molecules on platinum in the gas phase. An associated surface residence time can be linked to the dynamics and time scale required for self-organization.

2.
Biosens Bioelectron ; 21(9): 1746-52, 2006 Mar 15.
Article in English | MEDLINE | ID: mdl-16256328

ABSTRACT

The suitability of high resolution, in situ dc-sheet resistance monitoring (SRM) as a simplified and reliable sensing technique towards detection and tracking of protein immobilization has been explored. Non-specific adsorption of bovine serum albumin (BSA) onto a very thin gold film, acting as the sensing resistor, has been employed as a model system. For comparison, the novel sensing method was combined with surface plasmon resonance (SPR) spectroscopy, using the same flow cell and sensing surface. Two different, well known adsorption states, involving a composite layer of irreversibly and reversibly bound BSA, were clearly resolved by both methods. Clearly structured, pronounced and fully reproducible film resistance modulations have been resolved in the associated SRM data. The transition from reversibly bound BSA to the diluted protein phase is associated with an unusually large decrease in the dc-sheet resistance. The observed resistance modulation magnitude for an adsorbed BSA monolayer corresponds to approximately 1%, and up to 100 mOmega at a 10 Omega sensing resistor. The sheet resistance of irreversibly bound BSA was determined to 0.24 kOmega/cm2, and the associated specific resistivity estimated to 1-2x10(4) Omega cm.


Subject(s)
Biosensing Techniques/methods , Coated Materials, Biocompatible/analysis , Electric Impedance , Electrochemistry/methods , Materials Testing/methods , Metals/chemistry , Serum Albumin, Bovine/analysis , Adsorption , Biosensing Techniques/instrumentation , Coated Materials, Biocompatible/chemistry , Electrochemistry/instrumentation , Materials Testing/instrumentation , Microelectrodes , Protein Binding , Reproducibility of Results , Sensitivity and Specificity , Serum Albumin, Bovine/chemistry
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