2008
DOI: 10.1021/nl073144l
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Spatiotemporal Response of Living Cell Structures in Dictyostelium discoideum with Semiconductor Quantum Dots

Abstract: The ability to monitor the spatial and temporal organization of molecules such as biopolymers within a cell is essential to enable the ability to understand the complexity and dynamics existing in biological processes. However, many limitations currently exist in specifically labeling proteins in living cells. In our study, we incorporate nanometer-sized semiconductor quantum dots (QDs) into living cells for spatiotemporal protein imaging of actin polymers in Dictyostelium discoideum without the necessity of u… Show more

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Cited by 17 publications
(11 citation statements)
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“…Interest in NPs largely stems from their ability to carry a large therapeutic payload (or ample amounts of contrast agent), the ability to finely tune physicochemical properties, which can influence their pharmacokinetic and pharmacodynamic profiles, and the ability to functionalize their surface with molecularly specific targeting agents. For both diagnostic 1 and therapeutic 2 applications, it is becoming increasingly recognized that specific targeting of NPs is critical toward their effective use. When targeted, reduced amounts of therapeutic and imaging agents are required compared with systemically delivered vectors.…”
mentioning
confidence: 99%
“…Interest in NPs largely stems from their ability to carry a large therapeutic payload (or ample amounts of contrast agent), the ability to finely tune physicochemical properties, which can influence their pharmacokinetic and pharmacodynamic profiles, and the ability to functionalize their surface with molecularly specific targeting agents. For both diagnostic 1 and therapeutic 2 applications, it is becoming increasingly recognized that specific targeting of NPs is critical toward their effective use. When targeted, reduced amounts of therapeutic and imaging agents are required compared with systemically delivered vectors.…”
mentioning
confidence: 99%
“…It also allowed us confirm binding of HER2‐SPIO to cells via fluorescence microscopy and flow cytometry. Of course, aside from fluorophores other functional groups could also be incorporated onto the alkynated peptide and ultimately HER2‐SPIO, including haptens, metal chelates, chromophores, etc 17–19. As the size of these agents are relatively small, they are not expected to impede the efficiency of the EPL reaction.…”
Section: Discussionmentioning
confidence: 99%
“…Passive uptake of charged/functionalized QDs by semiconfluent cell layers has been documented when used at very high concentrations over long time periods. [32][33][34][35] The likelihood of this in our system is minimal since the stratified corneal epithelial cells were exposed to a low concentration of non-modified QDs for a short period of time. Some localization of QDs within the cytosol in corneal epithelial cells may also be attributed to Gprotein coupled receptor (GPCR) mediated endocytosis.…”
Section: Accepted Manuscriptmentioning
confidence: 99%