US2016169780A1PendingUtilityA1

Selective capture and release of analytes

Assignee: UNIV COLUMBIAPriority: Mar 27, 2007Filed: Dec 22, 2015Published: Jun 16, 2016
Est. expiryMar 27, 2027(~0.7 yrs left)· nominal 20-yr term from priority
C12Q 1/6816G01N 1/4055G01N 33/5308Y10T436/24Y10T436/25375Y10T436/143333G01N 21/6408
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Claims

Abstract

The described subject matter includes techniques and components for minimally invasive, selective capture and release of analytes. An aptamer is selected for its binding affinity with a particular analyte(s). The aptamer is functionalized on a solid phase, for example, microbeads, polymer monolith, microfabricated solid phase, etc. The analyte is allowed to bind to the aptamer, for example, in a microchamber. Once the analyte has been bound, a temperature control sets the temperature to an appropriate temperature at which the captured analyte is released.

Claims

exact text as granted — not AI-modified
1 . A method for capturing and selectively releasing an analyte, comprising:
 (a) binding the analyte to an aptamer, the aptamer functionalized on a solid phase; and   (b) setting the temperature of the aptamer such that the analyte is released from the aptamer.   
     
     
         2 . The method of  claim 1 , further comprising:
 (c) introducing the analyte to the aptamer in an impure form;   (d) washing the bound aptamer analyte complex to remove impurities; and   (e) repeating (c), (a), and (d) such that the amount of bound analyte is increased.   
     
     
         3 . The method of  claim 1 , further comprising:
 (f) collecting and detecting the analyte.   
     
     
         4 . The method of  claim 1 , wherein the detecting includes performing mass spectrometry on the released analyte. 
     
     
         5 . The method of  claim 1 , wherein the detecting includes detecting fluorescence intensity. 
     
     
         6 . The method of  claim 1 , wherein the solid phase includes a microbead. 
     
     
         7 . The method of  claim 1 , wherein the analyte includes an oligonucleotide. 
     
     
         8 . The method of  claim 1 , wherein binding the analyte to the aptamer comprising binding the analyte to the aptamer at a first temperature, and wherein setting the temperature of the aptamer comprises reducing the temperature of the aptamer to a second temperature which is lower than the first temperature. 
     
     
         9 . A method for selectively increasing the concentration of an analyte, comprising:
 (a) functionalizing a solid phase with an aptamer;   (b) introducing the analyte to the aptamer in an impure form;   (c) binding the analyte to the aptamer;   (d) washing the bound aptamer analyte complex to remove impurities;   (e) repeating (a)-(d) until a desired analyte concentration is reached; and   (f) setting the temperature of the aptamer such that the analyte is released from the aptamer.

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