Development of a Highly Active Fluorescence-based Detector for Yeast G Protein-Coupled Receptor Ste2p.
Author(s) -
JinWoo Hong,
Hee Jun Ahn,
Jee Su Baek,
Eun Young Hong,
DongHoon Jin,
Yong Ho Khang,
Namjoo Hong
Publication year - 2018
Publication title -
journal of microbiology and biotechnology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.601
H-Index - 64
ISSN - 1738-8872
DOI - 10.4014/jmb/1805.04045
Twenty analogs of [Orn,D-Ala]α-factor were synthesized and assayed for their biological activities: seven analogs of [Orn,X]α-factor, seven analogs of [X,D-Ala]α-factor, five analogs of [X,X,D-Ala]α-factor, and native α-factor (X = amino acids). Their biological activities (halo, gene induction, and affinity) were measured using S. cerevisiae Y7925 and LM102 and compared with those of native α-factor (100%). G protein-coupled receptor was expressed in strain LM102 containing pESC-LEU- vector. [Dap,D-Ala]α-factor with weak halo activity (10%) showed the highest receptor affinity (> 230%) and the highest gene induction activity (167%). [Arg,D-Ala]α-factor showed the highest halo activity (2,000%). The number of active binding sites per cell (about 20,000 for strain LM102) was determined using a newly designed fluorescence-based detector, [Arg,D-Ala]α-factor-Edan, with high sensitivity (12,500-fold higher than the absorption-based detector [Orn]α-factor-[Cys]).
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom