Neutralized Chimeric Avidin Binding at a Reference Biosensor Surface

doi:10.1021/la503213f

Neutralized Chimeric Avidin Binding at a Reference Biosensor Surface

2015-02-04

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DOI：10.1021/la503213f

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We describe the development of a reference biosensor surface, based upon a binary mixture of oligo-ethylene glycol thiols, one of which has biotin at the terminus, adsorbed onto gold as self-assembled monolayers (SAMs). These surfaces were analyzed in detail by X-ray photoelectron spectroscopy (XPS) and secondary ion mass spectrometry (SIMS) to establish the relationship between the thiol solution composition and the surface composition and structure. We report the use of argon cluster primary ions for the analysis of PEG-thiols, establishing that the different thiols are intimately mixed and that SIMS may be used to measure surface composition of thiol SAMs on gold with a detection limit better than 1% fractional coverage. The adsorption of neutralized chimeric avidin to these surfaces was measured simultaneously using ellipsometry and QCM-D. Comparison of the two measurements demonstrates the expected nonlinearity of the frequency response of the QCM but also reveals a strong variation in the dissipation signal that correlates with the surface density of biotin. These variations are most likely due to the difference in mechanical response of neutralized chimeric avidin bound by just one biotin moiety at low biotin density and two biotin moieties at high density. The transition between the two modes of binding occurs when the average spacing of biotin ligands approaches the diameter of the avidin molecule.

Keywords:

SELF-ASSEMBLED MONOLAYERS

ION MASS-SPECTROMETRY

PROTEIN ADSORPTION

GOLD NANOPARTICLES

OXIDE SURFACES

HIGH-AFFINITY

TOF-SIMS

BIOTIN

XPS

IMMOBILIZATION

Neutralized Chimeric Avidin Binding at a Reference Biosensor Surface

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