US2018163257A1PendingUtilityA1

Bioprobes and methods of use thereof

Assignee: GOVERNING COUNCIL UNIV TORONTOPriority: Feb 7, 2011Filed: Oct 6, 2017Published: Jun 14, 2018
Est. expiryFeb 7, 2031(~4.5 yrs left)· nominal 20-yr term from priority
C12Q 1/6816C12N 2310/3181G01N 27/3277C12Q 1/6886G01N 27/3276C12Q 2523/31C12Q 1/6837G01N 27/26
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Claims

Abstract

Disclosed are biomolecule based bioprobes that exhibit improved water solubility and mono layer-forming properties with substantially little or no aggregation that can appreciably interfere with binding of the bioprobes to a target nucleotide. The bioprobes may be used in conjunction with a suitable reporter system to detect very small quantities of biological markers. The bio-probes comprise a nucleobase sequence capable of hybridizing to a target nucleotide; and at least one charged functional group attached to said nucleobase sequence. Also disclosed are biosensors, and sensing devices that comprise the bin-probe. Further disclosed are suitable electrochemical reporter systems for use with the bioprobes. Methods of use of these devices and probes, including for the detection of target biomarkers, including biomarkers for cancer cells or pathogens, are also included.

Claims

exact text as granted — not AI-modified
1 . A bio-probe comprising:
 a nucleobase sequence capable of hybridizing to a target nucleotide; at least one charged functional group attached to said nucleobase sequence, wherein said charged functional group comprises a cationic functional group, an anionic functional group, a charged amino acid, or a combination thereof; and   wherein attachment of said charged functional group to said nucleobase results in lesser aggregation of a plurality of bio-probes, as compared to bio-probes not comprising a charged functional group attached to said nucleobase.   
     
     
         2 - 116 . (canceled)

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