A cDNA library functional screening strategy based on fluorescent protein complementation assays to identify novel components of signaling pathways

被引:66
作者
Remy, I [1 ]
Michnick, SW [1 ]
机构
[1] Univ Montreal, Dept Biochim, Montreal, PQ H3C 3J7, Canada
基金
加拿大健康研究院;
关键词
protein-fragment complementation assays; cDNA library screening; protein-protein interactions; green fluorescent protein;
D O I
10.1016/j.ymeth.2003.10.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Progress towards a deeper understanding of cellular biochemical networks demands the development of methods to both identify and validate component proteins of these networks. Here, we describe a cDNA library screening strategy that achieves these aims, based on a protein-fragment complementation assay (PCA) using green fluorescent protein (GFP) as a reporter. The strategy combines a simple cell-based cDNA-screening approach (interactions of a "bait" protein of interest with "prey" cDNA products) with Specific functional assays that use the same system and provide initial validation of the cDNA products as being biologically relevant. We applied this strategy to identify novel interacting partners of the protein kinase PKB/Akt. This method provides very general means of identifying and validating genes involved in any Cellular process and is particularly designed for identifying enzyme substrates or regulatory proteins for which the enzyme specificity can only be defined by their interactions with other proteins in cells in which the proteins are normally expressed. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:381 / 388
页数:8
相关论文
共 35 条
[1]   MOLECULAR-CLONING OF A CD28 CDNA BY A HIGH-EFFICIENCY COS CELL EXPRESSION SYSTEM [J].
ARUFFO, A ;
SEED, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (23) :8573-8577
[2]   Intracellular signalling: PDK1 - a kinase at the hub of things [J].
Belham, C ;
Wu, SL ;
Avruch, J .
CURRENT BIOLOGY, 1999, 9 (03) :R93-R96
[3]   PKB binding proteins: Getting in on the akt [J].
Brazil, DP ;
Park, J ;
Hemmings, BA .
CELL, 2002, 111 (03) :293-303
[4]   Ten years of protein kinase B signalling: a hard Akt to follow [J].
Brazil, DP ;
Hemmings, BA .
TRENDS IN BIOCHEMICAL SCIENCES, 2001, 26 (11) :657-664
[5]   EXPRESSION CLONING OF THE MURINE ERYTHROPOIETIN RECEPTOR [J].
DANDREA, AD ;
LODISH, HF ;
WONG, GG .
CELL, 1989, 57 (02) :277-285
[6]   Cellular survival: a play in three Akts [J].
Datta, SR ;
Brunet, A ;
Greenberg, ME .
GENES & DEVELOPMENT, 1999, 13 (22) :2905-2927
[7]   Progress and variations in two-hybrid and three-hybrid technologies [J].
Drees, BL .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1999, 3 (01) :64-70
[8]   A NOVEL GENETIC SYSTEM TO DETECT PROTEIN PROTEIN INTERACTIONS [J].
FIELDS, S ;
SONG, OK .
NATURE, 1989, 340 (6230) :245-246
[9]   Antiparallel leucine zipper-directed protein reassembly: Application to the green fluorescent protein [J].
Ghosh, I ;
Hamilton, AD ;
Regan, L .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2000, 122 (23) :5658-5659
[10]   Visualization of interactions among bZip and Rel family proteins in living cells using bimolecular fluorescence complementation [J].
Hu, CD ;
Chinenov, Y ;
Kerppola, TK .
MOLECULAR CELL, 2002, 9 (04) :789-798