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1.
Science ; 323(5910): 133-8, 2009 Jan 02.
Artículo en Inglés | MEDLINE | ID: mdl-19023044

RESUMEN

We present single-molecule, real-time sequencing data obtained from a DNA polymerase performing uninterrupted template-directed synthesis using four distinguishable fluorescently labeled deoxyribonucleoside triphosphates (dNTPs). We detected the temporal order of their enzymatic incorporation into a growing DNA strand with zero-mode waveguide nanostructure arrays, which provide optical observation volume confinement and enable parallel, simultaneous detection of thousands of single-molecule sequencing reactions. Conjugation of fluorophores to the terminal phosphate moiety of the dNTPs allows continuous observation of DNA synthesis over thousands of bases without steric hindrance. The data report directly on polymerase dynamics, revealing distinct polymerization states and pause sites corresponding to DNA secondary structure. Sequence data were aligned with the known reference sequence to assay biophysical parameters of polymerization for each template position. Consensus sequences were generated from the single-molecule reads at 15-fold coverage, showing a median accuracy of 99.3%, with no systematic error beyond fluorophore-dependent error rates.


Asunto(s)
ADN Polimerasa Dirigida por ADN/metabolismo , Análisis de Secuencia de ADN/métodos , Secuencia de Bases , Secuencia de Consenso , ADN/biosíntesis , ADN Circular/química , ADN de Cadena Simple/química , Desoxirribonucleótidos/metabolismo , Enzimas Inmovilizadas , Colorantes Fluorescentes , Cinética , Nanoestructuras , Espectrometría de Fluorescencia
2.
Opt Lett ; 33(9): 1026-8, 2008 May 01.
Artículo en Inglés | MEDLINE | ID: mdl-18451975

RESUMEN

The confocal detection principle is extended to a highly parallel optical system that continuously analyzes thousands of concurrent sample locations. This is achieved through the use of a holographic laser illumination multiplexer combined with a confocal pinhole array before a prism dispersive element used to provide spectroscopic information from each confocal volume. The system is demonstrated to detect and identify single fluorescent molecules from each of several thousand independent confocal volumes in real time.


Asunto(s)
Colorantes Fluorescentes/química , Nanotecnología , Microscopía Confocal/instrumentación , Microscopía Confocal/métodos
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