New Frontiers in Ultrasensitive Bioanalysis 2006
DOI: 10.1002/9780470119501.ch1
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Cited by 2 publications
(5 citation statements)
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“…Similar interesting phenomena were observed in our previous study, in which we directly observed such a complete binding reaction process as single nanoparticle biosensors diffused to the surface of cells, searched for receptors on the surface of the cells, attempted its binding with the receptors several times, and finally bound with the receptors . We did not observe immediate disassociation of ligand−receptor complex (Off-state), which could be attributable to the large affinity of the ligand−receptor complex ( K B = 4.3 × 10 7 M −1 ) that led to a long association time (On-rate), as predicted by simulations …”
Section: Resultssupporting
confidence: 86%
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“…Similar interesting phenomena were observed in our previous study, in which we directly observed such a complete binding reaction process as single nanoparticle biosensors diffused to the surface of cells, searched for receptors on the surface of the cells, attempted its binding with the receptors several times, and finally bound with the receptors . We did not observe immediate disassociation of ligand−receptor complex (Off-state), which could be attributable to the large affinity of the ligand−receptor complex ( K B = 4.3 × 10 7 M −1 ) that led to a long association time (On-rate), as predicted by simulations …”
Section: Resultssupporting
confidence: 86%
“…The result suggests that either single TNFα molecules did not disassociate from MAB on the surface of nanoparticles or the disassociated single TNFα molecules might be trapped among the surface functional groups (MMUA-PVP) of nanoparticles (Scheme ) and therefore were unable to depart from the surface of nanoparticles. The large binding constant ( K B = 1.7 × 10 6 M −1 ) of TNFα-MAB could hinder their disassociation (Off-state), leading to a long association time (On-rate) (>1.6 × 10 6 s = 444 h), as predicted by recent simulations . Similar interesting phenomena were observed in our previous study, in which we directly observed such a complete binding reaction process as single nanoparticle biosensors diffused to the surface of cells, searched for receptors on the surface of the cells, attempted its binding with the receptors several times, and finally bound with the receptors .…”
Section: Resultssupporting
confidence: 83%
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“…Recent studies show that 10-14 measurements of individual events (e.g., single molecules) are sufficient sample sizes to extrapolate ensemble properties with accuracy of analytical measurements at single-entity level. 39 Thus, the sample sizes presented in this study are adequate for the study of bulk cells at the single-cell resolution. Unlike ensemble measurements, single-cell imaging allows us to unmask the heterogeneous nature of individual cells in bulk solution and probe intracellular molecules and structures of individual cells with both spatial and temporal resolution.…”
Section: Discussionmentioning
confidence: 92%
“…Recent studies show that 10−14 measurements of individual events (e.g., single molecules) are sufficient sample sizes to extrapolate ensemble properties with accuracy of analytical measurements at single-entity level . Thus, the sample sizes presented in this study are adequate for the study of bulk cells at the single-cell resolution.…”
Section: Methodsmentioning
confidence: 88%