Abstract:
PURPOSE: A yeast strain library system for analyzing protein-protein interaction in yeast cell at genome-wide level is provided to quickly analyze the interaction of whole protein of yeast. CONSTITUTION: A gene recombinant Saccharomyces cerevisiae strain library contains yellow fluorescence protein N-terminal fragment gene which is operably linked to C-terminal on a genome DNA of Saccharomyces cerevisiae. A recombinant vector for substituting epitope tag has a sequence of sequence number 1 or 2.
Abstract:
PURPOSE: A yeast strain library system for analyzing protein-protein interaction in yeast cell at genome-wide level is provided to quickly analyze the interaction of whole protein of yeast. CONSTITUTION: A gene recombinant Saccharomyces cerevisiae strain library contains yellow fluorescence protein N-terminal fragment gene which is operably linked to C-terminal on a genome DNA of Saccharomyces cerevisiae. A recombinant vector for substituting epitope tag has a sequence of sequence number 1 or 2.
Abstract:
PURPOSE: A method for real time analysis of protein interaction in animal cells is provided to directly observe interaction and change between proteins by a microscope. CONSTITUTION: A method for measuring interaction of a protein comprises: a step of providing viral genome DNA by cloning a restriction enzyme recognition base sequence, two positions-specific recombinant enzyme recognition base sequence, and a gene encoding a first fragment of a reporter protein; a step of treating the viral genome DNA with a restriction enzyme to prepare two linear viral genome DNA fragments; a step of providing a transport vector containing DNA encoding a first target protein; a step of transducing the recombinant vector to a host cell to prepare the first recombinant virus; a step of providing a second recombinant virus containing a gene encoding a second fragment; and a step of infecting the first and second recombinant viruses to a target cells and measuring coloration.