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Surface Sensitization Techniques and Recognition Receptors Immobilization on Biosensors and Microarrays

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Recognition Receptors in Biosensors

Abstract

The quality of a biosensing system relies on the interfacial properties where bioactive species are immobilized. The design of the surface includes both the immobilization of the bioreceptor itself and the overall chemical preparation of the transducer surface. Hence, the sensitivity and specificity of such devices are directly related to the accessibility and activity of the immobilized molecules. The inertness of the surface that limits the nonspecific adsorption sets the background noise of the sensor. The specifications of the biosensor (signal-to-noise ratio) depend largely on the surface chemistry and preparation process of the biointerface. Lastly, a robust interface improves the stability and the reliability of biosensors. This chapter reports in detail the main surface coupling strategies spanning from random immobilization of native biospecies to uniform and oriented immobilization of site-specific modified biomolecules. The immobilization of receptors on various shapes of solid support is then introduced. Detection systems sensitive to surface phenomena require immobilization as very thin layers (two-dimensional biofunctionalization), whereas other detection systems accept thicker layers (three-dimensional biofunctionalization) such as porous materials of high specific area that lead to large increase of signal detection. This didactical overview introduces each step of the biofunctionalization with respect to the diversity of biological molecules, their accessibility and resistance to nonspecific adsorption at interfaces.

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Abbreviations

μ-TAS:

Micro-total analysis system

AAPS:

N-(2-aminoethyl)-3-aminopropyltrimethoxysilane

ALD:

Atomic layer deposition

APTS:

Aminopropyltriethoxysilane

Asp:

Aspartic acid

BSA:

Bovin serum albumin

DIOS:

Desorption/ionization on silicon

DMP:

Dimethyl pimelimidate

DMS:

Dimethyl suberimidate

DMSO:

Dimethylsulfoxide

DNA:

Desoxyribonucleic acid

DTT:

Dithiothreitol

EDTA:

Ethylenediamine tetraacetic

ELISA:

Enzyme-Linked immunosorbent assay

ENFET:

Enzymatic field-effect transistor

EPL:

Express protein ligation

ET:

Electron transfer

Glu:

Glutamic acid

GOD:

Glucose oxidase

GPTS:

3-glycidoxypropyltriethoxysilane

IDA:

Iminodiacetic acid

IPL:

Intein-mediated protein ligation

ISE:

Ion-selective electrodes

ISFET:

Ion-selective field-effect transistor

ITO:

Indium Titanium oxide

Lys:

Lysine

M2C2H:

4-(N-maleimidomethyl)cyclohexan-1-carboxylhydrazide

MALDI:

Matrix-assisted laser desorption/ionization

MESNA:

2-Mercaptoethansulfonate

MPAA:

(4-carboxymehtyl)thiophenol

mRNA:

Messenger ribonucleic acid

NCL:

Native Chemical Ligation

NHS:

N-hydroxysuccinimide

NTA:

Nitrolotriacetic acid

ODN:

Oligodesoxyribonucleotides

PAMAM:

Poly(amino)amine

PCP:

Peptide carrier protein

PCR:

Polymerase chain reaction

PDITC:

Phenylenediisothiocyanate

PDMS:

Polydimethylsiloxane

PEG:

Poly(ethylene glycol)

PNA:

Peptide nucleic acid

SAM:

Self-assembled monolayer

SIAB:

Succinimidyl 4-(N-iodoacetyl)aminobenzoate

SMCC:

Succinimidyl-4-(N-maleimidomethyl)cyclohexane-1-carboxylate

SMPB:

Succinimidyl-4-(N-maleimidophenyl)butyrate

SPDP:

N-succinimidyl-3(2-pyridyldithio)propionate

s-SIAB:

Sulfosuccinimidyl 4-(N-iodoacetyl)aminobenzoate

TCEP:

Tris(2-carboxyethyl)phosphine

TEOS:

Tetraethoxysilane

TMOS:

Tetramethoxysilane

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Dugas, V., Elaissari, A., Chevalier, Y. (2010). Surface Sensitization Techniques and Recognition Receptors Immobilization on Biosensors and Microarrays. In: Zourob, M. (eds) Recognition Receptors in Biosensors. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-0919-0_2

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