1993
DOI: 10.1063/1.465447
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Molecular recognition at self-assembled monolayers: Optimization of surface functionalization

Abstract: Articles you may be interested inUnderstanding the nonfouling mechanism of surfaces through molecular simulations of sugar-based selfassembled monolayers Nanostructural and electrical properties of functionally terminated self-assembled monolayers on silicon surfacesSulfur-based molecules containing biotin and hydroxyl groups have been used to create a wide variety of self-assembled monolayers on gold surfaces. Surface plasmon resonance has been used to study in situ the binding of streptavidin to these monola… Show more

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Cited by 315 publications
(306 citation statements)
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“…From avidin immobilization study together with the XPS results, we presume the absolute density of the attached biotin is not large even under the acidic pH, because it is well known that the largest yield of avidin immobilization is found at one tenth of a full monolayer density of biotin. 13 The exclusive pattern result from highly acidic pH indicates that the attachment of biotin hydrazide is negligible on the other electrodes and glass surfaces presenting the protected aldehyde, which supports a high spatial selectivity of our immobilization method based on electrochemical addressing.…”
Section: Methodssupporting
confidence: 63%
“…From avidin immobilization study together with the XPS results, we presume the absolute density of the attached biotin is not large even under the acidic pH, because it is well known that the largest yield of avidin immobilization is found at one tenth of a full monolayer density of biotin. 13 The exclusive pattern result from highly acidic pH indicates that the attachment of biotin hydrazide is negligible on the other electrodes and glass surfaces presenting the protected aldehyde, which supports a high spatial selectivity of our immobilization method based on electrochemical addressing.…”
Section: Methodssupporting
confidence: 63%
“…620 To explain the data, they invoked the concept of lateral steric effects [622][623][624][625][626][627] -an unfavorable steric repulsion between BCA II that is bound at the surface and BCA II that is free in solution ( Figure 10C; section 8.4.3). Decreasing the fractional coverage of arylsulfonamide ligands on the surface should reduce the possibility of these unfavorable interactions between bound BCA II molecules and increase the observed value of k on to its solution-phase value.…”
Section: Lateral Steric Effectsmentioning
confidence: 99%
“…35,36 11-Mercapto-1-undecanol, sodium chloride, monosodium phosphate ͑NaH 2 PO 4 ͒, disodium phosphate ͑Na 2 HPO 4 ͒, and absolute ethanol were purchased from Aldrich. The chemical structures and the sequences of the oligonucleotides used are summarized in Table I.…”
Section: A Materialsmentioning
confidence: 99%