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公开(公告)号:US11466312B2
公开(公告)日:2022-10-11
申请号:US16958683
申请日:2018-12-31
Applicant: KOREA ADVANCED INSTITUTE OF SCIENCE AND TECHNOLOGY , BIONANO HEALTH GUARD RESEARCH CENTER
Inventor: Hyun Gyu Park , Hyo Yong Kim , Yong Ju , Jun Ki Ahn
IPC: C12Q1/683
Abstract: The present invention relates to a detection method for detecting a target RNA contained in a sample with high sensitivity by using nicking/extension chain reaction system-based isothermal nucleic acid amplification (NESBA) that uses activity of a cleavage enzyme and a DNA polymerase. The NESBA of the present invention is a new concept isothermal target RNA detection method that realizes higher amplification efficiency than the existing NASBA technology and is deemed to be utilizable as a new concept diagnosis technology that can replace conventional target RNA detection technologies.
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公开(公告)号:US20180319835A1
公开(公告)日:2018-11-08
申请号:US15924242
申请日:2018-03-18
Applicant: KOREA ADVANCED INSTITUTE OF SCIENCE AND TECHNOLOGY , Gachon University of Industry-Academic cooperation Foundation
Inventor: Hyun Gyu Park , Moon Il Kim , Ki Soo Park , Chang Yeol Lee
Abstract: A method of preparing nucleic acid-inorganic hybrid nanoflowers is described, in which a nucleic acid is allowed to react with a solution of a metal ion-containing compound at room temperature, thereby forming a complex between the metal ion and the nitrogen atom of an amide bond or amine group present in the nucleic acid. Organic-inorganic hybrid nanoflower structures thus may be synthesized using nucleic acid in a simple manner under an environmentally friendly condition without any toxic chemical substance. The produced organic-inorganic hybrid nanoflower structures exhibit a high DNA encapsulation yield, nuclease resistance, and significantly increased peroxidase activity. These nanoflower structures may be widely used as gene therapy carriers and in biosensing technology.
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公开(公告)号:US10041111B2
公开(公告)日:2018-08-07
申请号:US15524093
申请日:2015-11-04
Inventor: Hyun Gyu Park , Ki Soo Park , Chang Yeol Lee
IPC: C12Q1/68 , C12N15/115 , C12Q1/6851
Abstract: The present invention relates to a method of detecting and quantifying biomolecules using nucleic acid polymerase activity controlled by the target molecule, and more particularly to a method for detecting or quantifying biomolecules, which can detect and quantify nucleic acids, proteins, small-molecular substances, physiologically active substances (enzymatic activities), etc., with high sensitivity, based on the change in DNA polymerase activity caused by specific binding of a specific nucleic acid that forms a complex with a DNA aptamer prepared so as to comprise a single-stranded DNA that specifically recognizes the specific nucleic acid. The present invention can provide a method for diagnosing biomolecules, which can detect and quantify target nucleic acids, target proteins, target small-molecular substances, target enzyme activities and the like in a label-free and sensitive manner by controlling polymerase activity through target molecule-induced conformational change of a DNA aptamer.
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公开(公告)号:US20170335381A1
公开(公告)日:2017-11-23
申请号:US15524093
申请日:2015-11-04
Inventor: Hyun Gyu Park , Ki Soo Park , Chang Yeol Lee
IPC: C12Q1/68 , C12N15/115
CPC classification number: C12Q1/6851 , C12N15/115 , C12N2310/16 , C12N2320/10 , C12Q1/6804 , C12Q1/6848 , C12Q2525/101 , C12Q2537/163 , C12Q2561/101 , C12Q2521/514 , C12Q2521/531 , C12Q2521/301
Abstract: The present invention relates to a method of detecting and quantifying biomolecules using nucleic acid polymerase activity controlled by the target molecule, and more particularly to a method for detecting or quantifying biomolecules, which can detect and quantify nucleic acids, proteins, small-molecular substances, physiologically active substances (enzymatic activities), etc., with high sensitivity, based on the change in DNA polymerase activity caused by specific binding of a specific nucleic acid that forms a complex with a DNA aptamer prepared so as to comprise a single-stranded DNA that specifically recognizes the specific nucleic acid. The present invention can provide a method for diagnosing biomolecules, which can detect and quantify target nucleic acids, target proteins, target small-molecular substances, target enzyme activities and the like in a label-free and sensitive manner by controlling polymerase activity through target molecule-induced conformational change of a DNA aptamer.
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