Optimized linkage and quenching strategies for quantum dot molecular beacons. Cady, N. C., Strickland, A. D., & Batt, C. A. Molecular and Cellular Probes, 21(2):116–124, April, 2007. ![Optimized linkage and quenching strategies for quantum dot molecular beacons [link]](https://bibbase.org/img/filetypes/link.svg "link")
Paper doi abstract bibtex Quantum dot (QD) molecular beacons were explored for sequence-specific DNA detection. The effectiveness of multiple linkage strategies and fluorescence quenchers were compared in hybridization-based assays. To compare linkage strategies, covalent amide linkage and streptavidin–biotin binding were used to link semiconductor QDs to molecular beacon DNA. Amide-linked beacons showed a 57% greater fluorescence increase than streptavidin-linked beacons when hybridized to 200 pmol of target DNA. The specificity of the molecular beacons, however, was similar for both linkage methods. Hybridization of both QD molecular beacons with non-complementary target DNA resulted in approximately 50% lower fluorescence intensity than hybridization with complementary DNA. The effectiveness of different quencher moieties was also evaluated. Iowa Black and 1.4 nm Nanogold-quenched molecular beacons exhibited approximately 2-fold greater fluorescence increases than dabcyl-quenched beacons when hybridized to complementary target. Specificity for target DNA was also confirmed through hybridization assays with non-complementary DNA. To provide insight into differences between the QD molecular beacons and the linkage strategies used, the hydrodynamic radius of each was measured. These measurements indicated that the larger radius of the streptavidin QDs (13.5 nm) than the carboxyl QDs (7 nm) could have a negative effect on FRET-based quenching for QD molecular beacons. These data outline the importance of choosing proper linkage methods and quencher moieties for creating high-quality QD molecular beacons.
@article{cady_optimized_2007,
title = {Optimized linkage and quenching strategies for quantum dot molecular beacons},
volume = {21},
issn = {0890-8508},
url = {http://www.sciencedirect.com/science/article/pii/S0890850806000636},
doi = {10.1016/j.mcp.2006.09.001},
abstract = {Quantum dot (QD) molecular beacons were explored for sequence-specific DNA detection. The effectiveness of multiple linkage strategies and fluorescence quenchers were compared in hybridization-based assays. To compare linkage strategies, covalent amide linkage and streptavidin–biotin binding were used to link semiconductor QDs to molecular beacon DNA. Amide-linked beacons showed a 57\% greater fluorescence increase than streptavidin-linked beacons when hybridized to 200\&\#xa0;pmol of target DNA. The specificity of the molecular beacons, however, was similar for both linkage methods. Hybridization of both QD molecular beacons with non-complementary target DNA resulted in approximately 50\% lower fluorescence intensity than hybridization with complementary DNA. The effectiveness of different quencher moieties was also evaluated. Iowa Black and 1.4\&\#xa0;nm Nanogold-quenched molecular beacons exhibited approximately 2-fold greater fluorescence increases than dabcyl-quenched beacons when hybridized to complementary target. Specificity for target DNA was also confirmed through hybridization assays with non-complementary DNA. To provide insight into differences between the QD molecular beacons and the linkage strategies used, the hydrodynamic radius of each was measured. These measurements indicated that the larger radius of the streptavidin QDs (13.5\&\#xa0;nm) than the carboxyl QDs (7\&\#xa0;nm) could have a negative effect on FRET-based quenching for QD molecular beacons. These data outline the importance of choosing proper linkage methods and quencher moieties for creating high-quality QD molecular beacons.},
number = {2},
urldate = {2012-05-11},
journal = {Molecular and Cellular Probes},
author = {Cady, Nathaniel C. and Strickland, Aaron D. and Batt, Carl A.},
month = apr,
year = {2007},
keywords = {Biosensor, DNA, Detection, Molecular beacon, Quantum dots},
pages = {116--124},
}
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The specificity of the molecular beacons, however, was similar for both linkage methods. Hybridization of both QD molecular beacons with non-complementary target DNA resulted in approximately 50% lower fluorescence intensity than hybridization with complementary DNA. The effectiveness of different quencher moieties was also evaluated. Iowa Black and 1.4 nm Nanogold-quenched molecular beacons exhibited approximately 2-fold greater fluorescence increases than dabcyl-quenched beacons when hybridized to complementary target. Specificity for target DNA was also confirmed through hybridization assays with non-complementary DNA. To provide insight into differences between the QD molecular beacons and the linkage strategies used, the hydrodynamic radius of each was measured. These measurements indicated that the larger radius of the streptavidin QDs (13.5 nm) than the carboxyl QDs (7 nm) could have a negative effect on FRET-based quenching for QD molecular beacons. These data outline the importance of choosing proper linkage methods and quencher moieties for creating high-quality QD molecular beacons.","number":"2","urldate":"2012-05-11","journal":"Molecular and Cellular Probes","author":[{"propositions":[],"lastnames":["Cady"],"firstnames":["Nathaniel","C."],"suffixes":[]},{"propositions":[],"lastnames":["Strickland"],"firstnames":["Aaron","D."],"suffixes":[]},{"propositions":[],"lastnames":["Batt"],"firstnames":["Carl","A."],"suffixes":[]}],"month":"April","year":"2007","keywords":"Biosensor, DNA, Detection, Molecular beacon, Quantum dots","pages":"116–124","bibtex":"@article{cady_optimized_2007,\n\ttitle = {Optimized linkage and quenching strategies for quantum dot molecular beacons},\n\tvolume = {21},\n\tissn = {0890-8508},\n\turl = {http://www.sciencedirect.com/science/article/pii/S0890850806000636},\n\tdoi = {10.1016/j.mcp.2006.09.001},\n\tabstract = {Quantum dot (QD) molecular beacons were explored for sequence-specific DNA detection. The effectiveness of multiple linkage strategies and fluorescence quenchers were compared in hybridization-based assays. To compare linkage strategies, covalent amide linkage and streptavidin–biotin binding were used to link semiconductor QDs to molecular beacon DNA. Amide-linked beacons showed a 57\\% greater fluorescence increase than streptavidin-linked beacons when hybridized to 200\\&\\#xa0;pmol of target DNA. The specificity of the molecular beacons, however, was similar for both linkage methods. Hybridization of both QD molecular beacons with non-complementary target DNA resulted in approximately 50\\% lower fluorescence intensity than hybridization with complementary DNA. The effectiveness of different quencher moieties was also evaluated. Iowa Black and 1.4\\&\\#xa0;nm Nanogold-quenched molecular beacons exhibited approximately 2-fold greater fluorescence increases than dabcyl-quenched beacons when hybridized to complementary target. Specificity for target DNA was also confirmed through hybridization assays with non-complementary DNA. To provide insight into differences between the QD molecular beacons and the linkage strategies used, the hydrodynamic radius of each was measured. These measurements indicated that the larger radius of the streptavidin QDs (13.5\\&\\#xa0;nm) than the carboxyl QDs (7\\&\\#xa0;nm) could have a negative effect on FRET-based quenching for QD molecular beacons. These data outline the importance of choosing proper linkage methods and quencher moieties for creating high-quality QD molecular beacons.},\n\tnumber = {2},\n\turldate = {2012-05-11},\n\tjournal = {Molecular and Cellular Probes},\n\tauthor = {Cady, Nathaniel C. and Strickland, Aaron D. and Batt, Carl A.},\n\tmonth = apr,\n\tyear = {2007},\n\tkeywords = {Biosensor, DNA, Detection, Molecular beacon, Quantum dots},\n\tpages = {116--124},\n}\n\n\n\n\n\n\n\n\n\n\n\n","author_short":["Cady, N. C.","Strickland, A. D.","Batt, C. 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