US2006014175A1PendingUtilityA1

Functionalized fluorescent nanocrystal detection system

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Assignee: NAASANI IMADPriority: May 17, 2004Filed: May 17, 2005Published: Jan 19, 2006
Est. expiryMay 17, 2024(expired)· nominal 20-yr term from priority
Inventors:Imad Naasani
G01N 33/588C12Q 1/48Y10S977/774Y10S977/902B82Y 15/00G01N 2333/9125
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Claims

Abstract

The present invention include fluorescent nanocrystals which have high fluorescence intensity, are water soluble, exhibit physical and chemical stability, and whose spectral properties are detectably modified as the size of functional groups bonded to the nanocrystal surface change when contacted with target molecules in a sample. The molecules in the sample add to or reduce the size of functional groups on the fluorescent nanocrystal proportional to the activity and amount of the target molecules. The present invention may be used to detect telomerase in a sample.

Claims

exact text as granted — not AI-modified
1 . A composition comprising: 
 one or more fluorescent nanocrystals;    a coating material comprising imidazole-containing molecules bonded by an imidazole group of the molecule to the surface of the fluorescent nanocrystals; and    one or more functional groups bonded to the coating material; the functional group bonded at a first end to the coating of the fluorescent nanocrystal, the second end of the functional groups extending from the nanocrystal coating where the spectral or physical properties of the fluorescent nanocrystal are modified by sequentially reacting of one or more of the functional groups with one or more target molecules in a sample.    
     
     
         2 . The composition of  claim 1  further comprising one or more acceptors or donors linked to the functional groups bonded to the coating material, the linked acceptor or donor exchanging energy with the fluorescent nanocrystal.  
     
     
         3 . The composition of  claim 1  where the functional groups comprise polynucleotides, polypeptides, glycoproteins, polysaccharides, lipoproteins, or combinations of these.  
     
     
         4 . The composition of  claim 1  where the fluorescent nanocrystal coating further comprises a cross linking agent  
     
     
         5 . The composition of  claim 1  where the fluorescent nanocrystal composition further comprises a buffer and the composition is at a temperature of about 37° or greater.  
     
     
         6 . The composition of  claim 1  where the fluorescent nanocrystal composition includes a transfecting agent and cells and wherein the functional groups bonded to the coating can be elongated or shortened in the cells.  
     
     
         7 . The composition of  claim 1  where the one or more functional groups comprise telomerase primers bonded to the coating material; the primers bonded at a first end to the coating of the nanocrystal, the second end of the primer extending from the nanocrystal coating, where the spectral or physical properties of the fluorescent nanocrystal are modified by sequential elongation of the primers when telomerase molecules are present in the sample.  
     
     
         8 . The composition of  claim 1  where reaction of one or more of the functional groups with one or more target molecules in a sample includes sequential elongation or shortening of the one or more functional groups.  
     
     
         9 . The composition of  claim 1  where the number of functional groups bonded to the coating is greater than about 100.  
     
     
         10 . The composition of  claim 1  where the coated fluorescent nanocrystals have a quantum yield of greater than 70%.  
     
     
         11 . A method comprising: 
 contacting a sample with fluorescent nanocrystals, the fluorescent nanocrystals comprising a coating of imidazole-containing molecules bonded by one or more of the imidazole group to the surface of the fluorescent nanocrystals, one or more functional groups bonded to the coating material; the functional groups bonded at a first end to the coating of the fluorescent nanocrystal, the second end of the functional groups extending from the nanocrystal coating where the spectral or physical properties of the fluorescent nanocrystal are modified by sequential reaction of one or more of the functional groups with one or more target molecules in a sample; and    correlating a change in the spectral or physical properties of the fluorescent nanocrystals in the sample with the sequential reaction of one or more of the functional groups with one or more target molecules in the sample.    
     
     
         12 . The method of  claim 11  where the target molecule is an enzyme.  
     
     
         13 . The method of  claim 11  where the reaction of the functional groups with target molecules results in sequential elongation or sequential shortening of the functional groups.  
     
     
         14 . The method of  claim 11  where the reaction of functional groups with target molecules results in the addition or removal of one or more acceptors or donors from the functional groups.  
     
     
         15 . The method of  claim 11  where the change in the spectral or physical properties of the fluorescent nanocrystals in the sample is related to the number of target molecules in the sample.  
     
     
         16 . The method of  claim 11  where the one or more functional groups comprise telomerase primers bonded to the coating material; the primers bonded at a first end to the coating of the nanocrystal, the second end of the primer extending from the nanocrystal coating, and where the change in the spectral or physical properties of the fluorescent nanocrystal are modified by sequential elongation of the primers reacting with a sample comprising telomerase molecules and nucleotides.  
     
     
         17 . The method of  claim 11  where reaction of the functional groups with the target molecules in the sample occurs at a temperature of about 20° C. or greater.  
     
     
         18 . The method of  claim 11  where the spectral property is energy transfer, Stokes shift, a polarization shift, or a combination of these.  
     
     
         19 . The method of  claim 11  where the one or more acceptors or donors linked to the functional groups bonded to the coating material exchange energy with the fluorescent nanocrystal.  
     
     
         20 . The method of  claim 16  where the nucleotides further include nucleotides with an acceptor or donor label.

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