New opportunities in multiplexed optical bioanalyses using quantum dots and donor–acceptor interactions
Abstract This review highlights recent trends in the development of multiplexed bioanalyses using quantum dot bioconjugates and donor–acceptor interactions. In these methods, multiple optical signals are generated in response to biorecognition through modulation of the photoluminescence of populatio...
Ausführliche Beschreibung
Autor*in: |
Algar, W. Russ [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2010 |
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Schlagwörter: |
Fluorescence resonance energy transfer |
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Anmerkung: |
© Springer-Verlag 2010 |
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Übergeordnetes Werk: |
Enthalten in: Analytical and bioanalytical chemistry - Berlin : Springer, 2002, 398(2010), 6 vom: 30. Mai, Seite 2439-2449 |
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Übergeordnetes Werk: |
volume:398 ; year:2010 ; number:6 ; day:30 ; month:05 ; pages:2439-2449 |
Links: |
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DOI / URN: |
10.1007/s00216-010-3837-y |
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Katalog-ID: |
SPR002194236 |
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520 | |a Abstract This review highlights recent trends in the development of multiplexed bioanalyses using quantum dot bioconjugates and donor–acceptor interactions. In these methods, multiple optical signals are generated in response to biorecognition through modulation of the photoluminescence of populations of quantum dots with different emission colors. The donor–acceptor interactions that have been used include fluorescence resonance energy transfer, bioluminescence resonance energy transfer, charge transfer quenching, and quenching via proximal gold nanoparticles. Assays for the simultaneous detection of between two and eight target analytes have been developed, where spectral deconvolution is an important tool. Target analytes have included small molecules, nucleic acid sequences, and proteases. The unique optical properties of quantum dots offer several potential advantages in multiplexed detection, and a large degree of versatility, for example, one pot multiplexing at the ensemble level, where only wavelength discrimination is required to differentiate between detection channels. These methods are not being developed to compete with array-based technologies in terms of overall multiplexing capacity, but rather to enable new formats for multiplexed bioanalyses. In particular, quantum dot bioprobes based on donor–acceptor interactions are anticipated to provide future opportunities for multiplexed biosensing within living cells. FigureMulticolor optical bioanalyses using donor-acceptor interactions between quantum dots and gold nanoparticles, fluorescent dyes, or redox active complexes. | ||
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700 | 1 | |a Krull, Ulrich J. |4 aut | |
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10.1007/s00216-010-3837-y doi (DE-627)SPR002194236 (SPR)s00216-010-3837-y-e DE-627 ger DE-627 rakwb eng Algar, W. Russ verfasserin aut New opportunities in multiplexed optical bioanalyses using quantum dots and donor–acceptor interactions 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2010 Abstract This review highlights recent trends in the development of multiplexed bioanalyses using quantum dot bioconjugates and donor–acceptor interactions. In these methods, multiple optical signals are generated in response to biorecognition through modulation of the photoluminescence of populations of quantum dots with different emission colors. The donor–acceptor interactions that have been used include fluorescence resonance energy transfer, bioluminescence resonance energy transfer, charge transfer quenching, and quenching via proximal gold nanoparticles. Assays for the simultaneous detection of between two and eight target analytes have been developed, where spectral deconvolution is an important tool. Target analytes have included small molecules, nucleic acid sequences, and proteases. The unique optical properties of quantum dots offer several potential advantages in multiplexed detection, and a large degree of versatility, for example, one pot multiplexing at the ensemble level, where only wavelength discrimination is required to differentiate between detection channels. These methods are not being developed to compete with array-based technologies in terms of overall multiplexing capacity, but rather to enable new formats for multiplexed bioanalyses. In particular, quantum dot bioprobes based on donor–acceptor interactions are anticipated to provide future opportunities for multiplexed biosensing within living cells. FigureMulticolor optical bioanalyses using donor-acceptor interactions between quantum dots and gold nanoparticles, fluorescent dyes, or redox active complexes. Quantum dots (dpeaa)DE-He213 Multiplexing (dpeaa)DE-He213 Fluorescence resonance energy transfer (dpeaa)DE-He213 Bioluminescence resonance energy transfer (dpeaa)DE-He213 Gold nanoparticles (dpeaa)DE-He213 Charge transfer quenching (dpeaa)DE-He213 Krull, Ulrich J. aut Enthalten in Analytical and bioanalytical chemistry Berlin : Springer, 2002 398(2010), 6 vom: 30. Mai, Seite 2439-2449 (DE-627)25372337X (DE-600)1459122-4 1618-2650 nnns volume:398 year:2010 number:6 day:30 month:05 pages:2439-2449 https://dx.doi.org/10.1007/s00216-010-3837-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 398 2010 6 30 05 2439-2449 |
spelling |
10.1007/s00216-010-3837-y doi (DE-627)SPR002194236 (SPR)s00216-010-3837-y-e DE-627 ger DE-627 rakwb eng Algar, W. Russ verfasserin aut New opportunities in multiplexed optical bioanalyses using quantum dots and donor–acceptor interactions 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2010 Abstract This review highlights recent trends in the development of multiplexed bioanalyses using quantum dot bioconjugates and donor–acceptor interactions. In these methods, multiple optical signals are generated in response to biorecognition through modulation of the photoluminescence of populations of quantum dots with different emission colors. The donor–acceptor interactions that have been used include fluorescence resonance energy transfer, bioluminescence resonance energy transfer, charge transfer quenching, and quenching via proximal gold nanoparticles. Assays for the simultaneous detection of between two and eight target analytes have been developed, where spectral deconvolution is an important tool. Target analytes have included small molecules, nucleic acid sequences, and proteases. The unique optical properties of quantum dots offer several potential advantages in multiplexed detection, and a large degree of versatility, for example, one pot multiplexing at the ensemble level, where only wavelength discrimination is required to differentiate between detection channels. These methods are not being developed to compete with array-based technologies in terms of overall multiplexing capacity, but rather to enable new formats for multiplexed bioanalyses. In particular, quantum dot bioprobes based on donor–acceptor interactions are anticipated to provide future opportunities for multiplexed biosensing within living cells. FigureMulticolor optical bioanalyses using donor-acceptor interactions between quantum dots and gold nanoparticles, fluorescent dyes, or redox active complexes. Quantum dots (dpeaa)DE-He213 Multiplexing (dpeaa)DE-He213 Fluorescence resonance energy transfer (dpeaa)DE-He213 Bioluminescence resonance energy transfer (dpeaa)DE-He213 Gold nanoparticles (dpeaa)DE-He213 Charge transfer quenching (dpeaa)DE-He213 Krull, Ulrich J. aut Enthalten in Analytical and bioanalytical chemistry Berlin : Springer, 2002 398(2010), 6 vom: 30. Mai, Seite 2439-2449 (DE-627)25372337X (DE-600)1459122-4 1618-2650 nnns volume:398 year:2010 number:6 day:30 month:05 pages:2439-2449 https://dx.doi.org/10.1007/s00216-010-3837-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 398 2010 6 30 05 2439-2449 |
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10.1007/s00216-010-3837-y doi (DE-627)SPR002194236 (SPR)s00216-010-3837-y-e DE-627 ger DE-627 rakwb eng Algar, W. Russ verfasserin aut New opportunities in multiplexed optical bioanalyses using quantum dots and donor–acceptor interactions 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2010 Abstract This review highlights recent trends in the development of multiplexed bioanalyses using quantum dot bioconjugates and donor–acceptor interactions. In these methods, multiple optical signals are generated in response to biorecognition through modulation of the photoluminescence of populations of quantum dots with different emission colors. The donor–acceptor interactions that have been used include fluorescence resonance energy transfer, bioluminescence resonance energy transfer, charge transfer quenching, and quenching via proximal gold nanoparticles. Assays for the simultaneous detection of between two and eight target analytes have been developed, where spectral deconvolution is an important tool. Target analytes have included small molecules, nucleic acid sequences, and proteases. The unique optical properties of quantum dots offer several potential advantages in multiplexed detection, and a large degree of versatility, for example, one pot multiplexing at the ensemble level, where only wavelength discrimination is required to differentiate between detection channels. These methods are not being developed to compete with array-based technologies in terms of overall multiplexing capacity, but rather to enable new formats for multiplexed bioanalyses. In particular, quantum dot bioprobes based on donor–acceptor interactions are anticipated to provide future opportunities for multiplexed biosensing within living cells. FigureMulticolor optical bioanalyses using donor-acceptor interactions between quantum dots and gold nanoparticles, fluorescent dyes, or redox active complexes. Quantum dots (dpeaa)DE-He213 Multiplexing (dpeaa)DE-He213 Fluorescence resonance energy transfer (dpeaa)DE-He213 Bioluminescence resonance energy transfer (dpeaa)DE-He213 Gold nanoparticles (dpeaa)DE-He213 Charge transfer quenching (dpeaa)DE-He213 Krull, Ulrich J. aut Enthalten in Analytical and bioanalytical chemistry Berlin : Springer, 2002 398(2010), 6 vom: 30. Mai, Seite 2439-2449 (DE-627)25372337X (DE-600)1459122-4 1618-2650 nnns volume:398 year:2010 number:6 day:30 month:05 pages:2439-2449 https://dx.doi.org/10.1007/s00216-010-3837-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 398 2010 6 30 05 2439-2449 |
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10.1007/s00216-010-3837-y doi (DE-627)SPR002194236 (SPR)s00216-010-3837-y-e DE-627 ger DE-627 rakwb eng Algar, W. Russ verfasserin aut New opportunities in multiplexed optical bioanalyses using quantum dots and donor–acceptor interactions 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2010 Abstract This review highlights recent trends in the development of multiplexed bioanalyses using quantum dot bioconjugates and donor–acceptor interactions. In these methods, multiple optical signals are generated in response to biorecognition through modulation of the photoluminescence of populations of quantum dots with different emission colors. The donor–acceptor interactions that have been used include fluorescence resonance energy transfer, bioluminescence resonance energy transfer, charge transfer quenching, and quenching via proximal gold nanoparticles. Assays for the simultaneous detection of between two and eight target analytes have been developed, where spectral deconvolution is an important tool. Target analytes have included small molecules, nucleic acid sequences, and proteases. The unique optical properties of quantum dots offer several potential advantages in multiplexed detection, and a large degree of versatility, for example, one pot multiplexing at the ensemble level, where only wavelength discrimination is required to differentiate between detection channels. These methods are not being developed to compete with array-based technologies in terms of overall multiplexing capacity, but rather to enable new formats for multiplexed bioanalyses. In particular, quantum dot bioprobes based on donor–acceptor interactions are anticipated to provide future opportunities for multiplexed biosensing within living cells. FigureMulticolor optical bioanalyses using donor-acceptor interactions between quantum dots and gold nanoparticles, fluorescent dyes, or redox active complexes. Quantum dots (dpeaa)DE-He213 Multiplexing (dpeaa)DE-He213 Fluorescence resonance energy transfer (dpeaa)DE-He213 Bioluminescence resonance energy transfer (dpeaa)DE-He213 Gold nanoparticles (dpeaa)DE-He213 Charge transfer quenching (dpeaa)DE-He213 Krull, Ulrich J. aut Enthalten in Analytical and bioanalytical chemistry Berlin : Springer, 2002 398(2010), 6 vom: 30. Mai, Seite 2439-2449 (DE-627)25372337X (DE-600)1459122-4 1618-2650 nnns volume:398 year:2010 number:6 day:30 month:05 pages:2439-2449 https://dx.doi.org/10.1007/s00216-010-3837-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 398 2010 6 30 05 2439-2449 |
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10.1007/s00216-010-3837-y doi (DE-627)SPR002194236 (SPR)s00216-010-3837-y-e DE-627 ger DE-627 rakwb eng Algar, W. Russ verfasserin aut New opportunities in multiplexed optical bioanalyses using quantum dots and donor–acceptor interactions 2010 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier © Springer-Verlag 2010 Abstract This review highlights recent trends in the development of multiplexed bioanalyses using quantum dot bioconjugates and donor–acceptor interactions. In these methods, multiple optical signals are generated in response to biorecognition through modulation of the photoluminescence of populations of quantum dots with different emission colors. The donor–acceptor interactions that have been used include fluorescence resonance energy transfer, bioluminescence resonance energy transfer, charge transfer quenching, and quenching via proximal gold nanoparticles. Assays for the simultaneous detection of between two and eight target analytes have been developed, where spectral deconvolution is an important tool. Target analytes have included small molecules, nucleic acid sequences, and proteases. The unique optical properties of quantum dots offer several potential advantages in multiplexed detection, and a large degree of versatility, for example, one pot multiplexing at the ensemble level, where only wavelength discrimination is required to differentiate between detection channels. These methods are not being developed to compete with array-based technologies in terms of overall multiplexing capacity, but rather to enable new formats for multiplexed bioanalyses. In particular, quantum dot bioprobes based on donor–acceptor interactions are anticipated to provide future opportunities for multiplexed biosensing within living cells. FigureMulticolor optical bioanalyses using donor-acceptor interactions between quantum dots and gold nanoparticles, fluorescent dyes, or redox active complexes. Quantum dots (dpeaa)DE-He213 Multiplexing (dpeaa)DE-He213 Fluorescence resonance energy transfer (dpeaa)DE-He213 Bioluminescence resonance energy transfer (dpeaa)DE-He213 Gold nanoparticles (dpeaa)DE-He213 Charge transfer quenching (dpeaa)DE-He213 Krull, Ulrich J. aut Enthalten in Analytical and bioanalytical chemistry Berlin : Springer, 2002 398(2010), 6 vom: 30. Mai, Seite 2439-2449 (DE-627)25372337X (DE-600)1459122-4 1618-2650 nnns volume:398 year:2010 number:6 day:30 month:05 pages:2439-2449 https://dx.doi.org/10.1007/s00216-010-3837-y lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_SPRINGER SSG-OLC-PHA GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_32 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 GBV_ILN_73 GBV_ILN_74 GBV_ILN_90 GBV_ILN_95 GBV_ILN_100 GBV_ILN_101 GBV_ILN_105 GBV_ILN_110 GBV_ILN_120 GBV_ILN_138 GBV_ILN_150 GBV_ILN_151 GBV_ILN_152 GBV_ILN_161 GBV_ILN_170 GBV_ILN_171 GBV_ILN_187 GBV_ILN_206 GBV_ILN_213 GBV_ILN_224 GBV_ILN_230 GBV_ILN_250 GBV_ILN_281 GBV_ILN_285 GBV_ILN_293 GBV_ILN_370 GBV_ILN_602 GBV_ILN_636 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2004 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2007 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2026 GBV_ILN_2027 GBV_ILN_2031 GBV_ILN_2034 GBV_ILN_2037 GBV_ILN_2038 GBV_ILN_2039 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2049 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2059 GBV_ILN_2061 GBV_ILN_2064 GBV_ILN_2065 GBV_ILN_2068 GBV_ILN_2070 GBV_ILN_2086 GBV_ILN_2088 GBV_ILN_2093 GBV_ILN_2106 GBV_ILN_2107 GBV_ILN_2108 GBV_ILN_2110 GBV_ILN_2111 GBV_ILN_2112 GBV_ILN_2113 GBV_ILN_2116 GBV_ILN_2118 GBV_ILN_2119 GBV_ILN_2122 GBV_ILN_2129 GBV_ILN_2143 GBV_ILN_2144 GBV_ILN_2147 GBV_ILN_2148 GBV_ILN_2152 GBV_ILN_2153 GBV_ILN_2188 GBV_ILN_2190 GBV_ILN_2232 GBV_ILN_2336 GBV_ILN_2360 GBV_ILN_2446 GBV_ILN_2470 GBV_ILN_2507 GBV_ILN_2522 GBV_ILN_2548 GBV_ILN_4012 GBV_ILN_4035 GBV_ILN_4037 GBV_ILN_4046 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4242 GBV_ILN_4246 GBV_ILN_4249 GBV_ILN_4251 GBV_ILN_4277 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4326 GBV_ILN_4328 GBV_ILN_4333 GBV_ILN_4334 GBV_ILN_4335 GBV_ILN_4336 GBV_ILN_4338 GBV_ILN_4393 GBV_ILN_4700 AR 398 2010 6 30 05 2439-2449 |
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Enthalten in Analytical and bioanalytical chemistry 398(2010), 6 vom: 30. Mai, Seite 2439-2449 volume:398 year:2010 number:6 day:30 month:05 pages:2439-2449 |
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Russ</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">New opportunities in multiplexed optical bioanalyses using quantum dots and donor–acceptor interactions</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2010</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">Computermedien</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Online-Ressource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Springer-Verlag 2010</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract This review highlights recent trends in the development of multiplexed bioanalyses using quantum dot bioconjugates and donor–acceptor interactions. In these methods, multiple optical signals are generated in response to biorecognition through modulation of the photoluminescence of populations of quantum dots with different emission colors. The donor–acceptor interactions that have been used include fluorescence resonance energy transfer, bioluminescence resonance energy transfer, charge transfer quenching, and quenching via proximal gold nanoparticles. Assays for the simultaneous detection of between two and eight target analytes have been developed, where spectral deconvolution is an important tool. Target analytes have included small molecules, nucleic acid sequences, and proteases. The unique optical properties of quantum dots offer several potential advantages in multiplexed detection, and a large degree of versatility, for example, one pot multiplexing at the ensemble level, where only wavelength discrimination is required to differentiate between detection channels. 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Algar, W. Russ misc Quantum dots misc Multiplexing misc Fluorescence resonance energy transfer misc Bioluminescence resonance energy transfer misc Gold nanoparticles misc Charge transfer quenching New opportunities in multiplexed optical bioanalyses using quantum dots and donor–acceptor interactions |
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New opportunities in multiplexed optical bioanalyses using quantum dots and donor–acceptor interactions Quantum dots (dpeaa)DE-He213 Multiplexing (dpeaa)DE-He213 Fluorescence resonance energy transfer (dpeaa)DE-He213 Bioluminescence resonance energy transfer (dpeaa)DE-He213 Gold nanoparticles (dpeaa)DE-He213 Charge transfer quenching (dpeaa)DE-He213 |
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new opportunities in multiplexed optical bioanalyses using quantum dots and donor–acceptor interactions |
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New opportunities in multiplexed optical bioanalyses using quantum dots and donor–acceptor interactions |
abstract |
Abstract This review highlights recent trends in the development of multiplexed bioanalyses using quantum dot bioconjugates and donor–acceptor interactions. In these methods, multiple optical signals are generated in response to biorecognition through modulation of the photoluminescence of populations of quantum dots with different emission colors. The donor–acceptor interactions that have been used include fluorescence resonance energy transfer, bioluminescence resonance energy transfer, charge transfer quenching, and quenching via proximal gold nanoparticles. Assays for the simultaneous detection of between two and eight target analytes have been developed, where spectral deconvolution is an important tool. Target analytes have included small molecules, nucleic acid sequences, and proteases. The unique optical properties of quantum dots offer several potential advantages in multiplexed detection, and a large degree of versatility, for example, one pot multiplexing at the ensemble level, where only wavelength discrimination is required to differentiate between detection channels. These methods are not being developed to compete with array-based technologies in terms of overall multiplexing capacity, but rather to enable new formats for multiplexed bioanalyses. In particular, quantum dot bioprobes based on donor–acceptor interactions are anticipated to provide future opportunities for multiplexed biosensing within living cells. FigureMulticolor optical bioanalyses using donor-acceptor interactions between quantum dots and gold nanoparticles, fluorescent dyes, or redox active complexes. © Springer-Verlag 2010 |
abstractGer |
Abstract This review highlights recent trends in the development of multiplexed bioanalyses using quantum dot bioconjugates and donor–acceptor interactions. In these methods, multiple optical signals are generated in response to biorecognition through modulation of the photoluminescence of populations of quantum dots with different emission colors. The donor–acceptor interactions that have been used include fluorescence resonance energy transfer, bioluminescence resonance energy transfer, charge transfer quenching, and quenching via proximal gold nanoparticles. Assays for the simultaneous detection of between two and eight target analytes have been developed, where spectral deconvolution is an important tool. Target analytes have included small molecules, nucleic acid sequences, and proteases. The unique optical properties of quantum dots offer several potential advantages in multiplexed detection, and a large degree of versatility, for example, one pot multiplexing at the ensemble level, where only wavelength discrimination is required to differentiate between detection channels. These methods are not being developed to compete with array-based technologies in terms of overall multiplexing capacity, but rather to enable new formats for multiplexed bioanalyses. In particular, quantum dot bioprobes based on donor–acceptor interactions are anticipated to provide future opportunities for multiplexed biosensing within living cells. FigureMulticolor optical bioanalyses using donor-acceptor interactions between quantum dots and gold nanoparticles, fluorescent dyes, or redox active complexes. © Springer-Verlag 2010 |
abstract_unstemmed |
Abstract This review highlights recent trends in the development of multiplexed bioanalyses using quantum dot bioconjugates and donor–acceptor interactions. In these methods, multiple optical signals are generated in response to biorecognition through modulation of the photoluminescence of populations of quantum dots with different emission colors. The donor–acceptor interactions that have been used include fluorescence resonance energy transfer, bioluminescence resonance energy transfer, charge transfer quenching, and quenching via proximal gold nanoparticles. Assays for the simultaneous detection of between two and eight target analytes have been developed, where spectral deconvolution is an important tool. Target analytes have included small molecules, nucleic acid sequences, and proteases. The unique optical properties of quantum dots offer several potential advantages in multiplexed detection, and a large degree of versatility, for example, one pot multiplexing at the ensemble level, where only wavelength discrimination is required to differentiate between detection channels. These methods are not being developed to compete with array-based technologies in terms of overall multiplexing capacity, but rather to enable new formats for multiplexed bioanalyses. In particular, quantum dot bioprobes based on donor–acceptor interactions are anticipated to provide future opportunities for multiplexed biosensing within living cells. FigureMulticolor optical bioanalyses using donor-acceptor interactions between quantum dots and gold nanoparticles, fluorescent dyes, or redox active complexes. © Springer-Verlag 2010 |
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title_short |
New opportunities in multiplexed optical bioanalyses using quantum dots and donor–acceptor interactions |
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https://dx.doi.org/10.1007/s00216-010-3837-y |
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Krull, Ulrich J. |
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|
score |
7.40059 |