A reversible Renilla luciferase protein complementation assay for rapid identification of protein-protein interactions reveals the existence of an interaction network involved in xyloglucan biosynthesis in the plant Golgi apparatus

Journal of Experimental Botany

Volumn 66, Issue 1, 2015, Pages 85-97

  Lund, Christian H ^a   Bromley, Jennifer R ^a,b,c,e   Stenbæk, Anne ^a,f   Rasmussen, Randi E ^a   Scheller, Henrik V ^b,c,d   Sakuragi, Yumiko ^a  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

^b JOINT BIOENERGY INSTITUTE   (United States)

^c LAWRENCE BERKELEY NATIONAL LABORATORY   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e Plant Biotechnology Division GRandD Cambridge British American Tobacco   (United Kingdom)

^f NOVOZYMES A S   (Denmark)

Author keywords

Arabidopsis thaliana; Glycosyltransferase; Golgi apparatus; Nicotiana benthamiana; Plant cell wall; Polysaccharides; Protein protein interaction; Renilla luciferase; Type II membrane protein; Xyloglucan

Indexed keywords

ARABIDOPSIS THALIANA; NICOTIANA BENTHAMIANA; RENILLA LUCIFERASE;

GLUCAN; PLANT PROTEIN; RENILLA LUCIFERIN 2 MONOOXYGENASE; XYLAN; XYLOGLUCAN;

AGROBACTERIUM TUMEFACIENS; BIOSYNTHESIS; GENETIC ENGINEERING; GENETICS; GOLGI COMPLEX; METABOLISM; PROCEDURES; PROTEIN ANALYSIS; TOBACCO;

AGROBACTERIUM TUMEFACIENS; GENETIC ENGINEERING; GLUCANS; GOLGI APPARATUS; LUCIFERASES, RENILLA; PLANT PROTEINS; PROTEIN INTERACTION MAPPING; TOBACCO; XYLANS;

EID: 84922561653     PISSN: 00220957     EISSN: 14602431     Source Type: Journal    
DOI: 10.1093/jxb/eru401     Document Type: Article

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