METHOD AND APPARATUS FOR DETERMINING AN ANALYTE PARAMETER
A method of determining an analyte parameter is described for an analyte in a detection region having at least one analyte binding zone. The method includes detecting presence of an analyte element bound at the binding zone, incrementing or decrementing a count and preventing recount of the element to obtain absolute quantification.
1 . A method of determining an analyte parameter for an analyte in a detection region having at least one analyte binding zone, the method comprising detecting presence of an analyte element bound at the binding zone, incrementing or decrementing an analyte element count and preventing recount of said element.
2 . A method as claimed in claim 1 in which the analyte element comprises a single molecule.
3 . A method as claimed in claim 1 in which the analyte element comprises a biological molecule, such as protein, glycoprotein, post translational modifications of proteins, DNA and mRNA.
4 . A method as claimed in claim 1 in which the detection region comprises a confined region.
5 . A method as claimed in claim 4 in which the detection region is provided on a micro fluidic device.
6 . A method as claimed in claim 1 in which the analyte binding zone comprises an affinity patch.
7 . A method as claimed in claim 6 in which a plurality of affinity patches are provided, and presence of an analyte element is detected at each affinity patch.
8 . A method as claimed in claim 1 in which the analyte comprises a cell protein.
9 . A method as claimed in claim 8 in which the cell is trapped in the detection region and optically or chemical lysed to release the cell protein.
10 . The method as claimed in claim 1 in which the analyte parameter comprises the number of analyte elements detected.
11 . A method as claimed in claim 1 in which recount is prevented by bleaching a detected analyte element.
12 . A method as claimed in claim 1 in which recount is prevented by image comparison.
13 . A method as claimed in claim 12 in which the image comparison step comprises a sequential image subtraction step.
14 . A method as claimed in claim 1 in which analyte element fluorescence is detected.
15 . A method as claimed in claim 1 in which the analyte is presented to the binding zone in one of a static hybridisation or continuous flow regimes.
16 . A method as claimed in claim 1 in which the analyte is bound to a liquid phase material at the binding zone.
17 . A method of extrapolating concentration of an analyte comprising a method as claimed in claim 1 and further comprising monitoring the rate of binding over time.
18 . An analysis device comprising an analyte chamber having at least one analyte binding zone provided.
19 . The device as claimed in claim 18 in which the analyte binding zone comprises an affinity patch.
20 . A device as claimed in claim 18 comprising a micro fluidic device.
21 . An analysis apparatus comprising an analysis device as claimed in claim 18 and further comprising a detector arranged to detect presence of an analyte element bound at the binding zone.
22 . An apparatus as claimed in claim 21 further comprising a processor for receiving a signal from said detector indicative of the presence of an analyte element and further arranged to increment an analyte element count upon receipt of said signal.
23 . An apparatus as claimed in claim 22 in which the processor is further arranged to prevent recount of said element in an image comparison step.
24 . A computer program comprising instructions for implementing the method of claim 1 .
25 . A computer readable medium for storing the computer program of claim 24 .
26 . A method of counting single molecules of un-amplified mRNA, detecting a biomarker from biological serum, performing single cell proteomics or monitoring a protein—protein interaction comprising the method of claim 1 .
27 . A method, device or apparatus substantially as described herein.