发明名称 Method and apparatus for analyzing protein-protein interaction on single-molecule level within the cellular environment
摘要 A method of analyzing protein-protein interactions includes binding the first proteins to the substrate where the first proteins are tagged with the first markers which bind specifically to the biomolecules immobilized on the substrate or the first proteins bind specifically to the biomolecules immobilized on the substrate; incubating the substrate bound first proteins with cell lysate containing the second proteins which are tagged with second markers; analyzing the interactions between the first proteins and the second proteins in the cell lysate, and obtaining the first analytic value representing the kinetic picture of the interactions; incubating the substrate bound first proteins with cell lysate mixture of a cell lysate consisting of the second markers-tagged second proteins and another cell lysate comprising other proteins including unlabelled second proteins and obtaining the second analytic value; comparing and analyzing the first and the second analytic values.
申请公布号 US9423400(B2) 申请公布日期 2016.08.23
申请号 US201314059349 申请日期 2013.10.21
申请人 KOREA ADVANCED INSTITUTE OF SCIENCE AND TECHNOLOGY 发明人 Yoon Tae-Young
分类号 G01N31/00;G01N33/53;G01N33/574;G01N33/68;G01N21/64 主分类号 G01N31/00
代理机构 Lex IP Meister, PLLC 代理人 Lex IP Meister, PLLC
主权项 1. A method of analyzing protein interactions between first proteins and second proteins at a single molecule level, comprising: (a) attaching biomolecules that bind specifically to first markers included in first proteins to a substrate; (b) supplying the first proteins tagged with first markers to the substrate to induce binding between the first marker and the biomolecules attached to the substrate; (c) supplying a cell lysate including the second proteins tagged with second markers to the substrate to induce the interactions between the first proteins and the second proteins after the biomolecules are bound to the first markers; (d) analyzing the interactions between the first proteins and the second proteins by measuring a fluorescent signal having a specific wavelength generated by the second markers tagged to the second proteins bound to the first protein using an optical apparatus generating a near-field wherein the fluorescent signal is measured cumulatively for a predetermined integral time period.
地址 Daejeon KR