Integrated analytical system and method
An analytical assembly within a unified device structure for integration into an analytical system. The analytical assembly is scalable and includes a plurality of analytical devices, each of which includes a reaction cell, an optical sensor, and at least one optical element positioned in optical communication with both the reaction cell and the sensor and which delivers optical signals from the cell to the sensor. Additional elements are optionally integrated into the analytical assembly. Methods for forming and operating the analytical system are also disclosed.
1. A method for sequencing a plurality of template nucleic acid molecules comprising:
adding a sequencing reaction mixture comprising reagents for carrying out polymerase dependent nucleic acid synthesis, including fluorescently labeled nucleotides, to the fluidic layer of an optode array chip;
wherein the optode array chip comprises a two dimensional array of optode elements, each optode element comprising:
a nanoscale aperture within an aperture layer, the aperture forming a fluid receiving nanoscale well for receiving a fluid including sequencing reagents;
above the aperture layer a fluidic layer in fluidic contact with the nanoscale well;
below the aperture layer a waveguide layer that provides illumination to the nanoscale well, the waveguide layer comprising an array of channel waveguides, each channel waveguide extending across a plurality of optode elements;
below the waveguide layer a transmission layer that transmits light emitted from the fluorescent species in the nanoscale well to a detector layer; and
below the transmission layer the detector layer comprising a detector which receives and detects the emitted light from the nanoscale well and transmitted through the transmission layer;
wherein a plurality of the nanoscale wells have within them a single polymerase-template complex comprising a polymerase enzyme and a template nucleic acid;
providing illumination to waveguides on the chip to illuminate optode array elements;
detecting fluorescent light emitted from the nanoscale wells using the detectors in the detector layer;
transmitting electrical signals from the detectors off of the chip through electrical contacts on the chip, and
processing the signals from the detectors in order to sequence a plurality of template nucleic acid molecules.
2. The method of claim 1 wherein each optode element further comprises a lens or an optical tunnel that preferentially directs optical signals from the nanoscale well to the detector.
3. The method of claim 1 wherein the chip comprises from about 1000 to about one million optode elements.
4. The method of claim 1 wherein the detector layer comprises embedded circuits for processing output data from the detector.
5. The method of claim 4 wherein the embedded circuits filter background noise from the detector.
6. The method of claim 4 further comprising an amplifier for amplifying the output data.
7. The method of claim 4 wherein embedded circuits comprise an analog to digital converter.
8. The method of claim 1 wherein there is little or no free space between the aperture, waveguide and transmission layers.
9. The method of claim 1 wherein the detector layer can be reversibly separated from the portion of the array comprising the aperture layer.
10. The method of claim 1 wherein the processing is carried out using a plurality of optional field programmable gate array (FPGA) blocks and application-specific integrated circuits (ASIC).
11. The method of claim 1 wherein the processing is carried out using a central processing unit (CPU) for processing data and controlling the system.
12. The method of claim 1 wherein the transmission layer comprises a filter, prism, grating, or dispersive optical elements to differentially direct different spectral components to different regions of the detector.
13. The method of claim 1 wherein each optode element has one, two, three, or four pixel elements.
14. The method of claim 1 wherein the illumination provided by the waveguide layer is modulated or interleaved to identify two or more different fluorescently labeled nucleotide.