Yeast two-hybrid: So many interactions, (in) so little time ...

被引:98
作者
Young, KH [1 ]
机构
[1] Amer Cyanamid Co, Mol Genet Screen Design, Princeton, NJ 08543 USA
关键词
D O I
10.1095/biolreprod58.2.302
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Protein-protein interactions are essential to cellular mechanisms at all levels in biologically responsive systems. These interactions occur extracellularly and include ligand-receptor interactions, cell adhesion, antigen recognition, and virus-host recognition. Intracellular protein-protein interactions occur in the formation of multi-protein complexes, during the assembly of cytoskeletal elements, and between receptor-effector, as well as effector-effector, molecules of signal transduction pathways. Finally, assembly of transcriptional machinery involves protein interactions. The yeast two-hybrid method is a powerful technique for analyzing these protein-protein interactions. Since the publication of this technique in the late 1980s, the robust nature and far-reaching utility of yeast two-hybrid systems for functional expression library cloning has led to the identification of many novel proteins in all areas of biological life science research. Additionally, two-hybrid techniques provide a rapid and versatile system for the further characterization of discrete protein-protein interactions. Recent variations on the basic system have enabled application well beyond protein pairs, to investigate multi-protein complexes and protein-nucleotide interactions. Yeast two-hybrid methods necessitate expression and subsequent interaction between a "protein of interest" functional pair within the yeast cell, ultimately driving reporter gene expression and thus effectively linking protein-protein interaction(s) to a change in yeast cell phenotype. functional protein-protein interactions using the two-hybrid techniques have been demonstrated for all levels of cellular biology; however, until recently, extracellular protein-protein interactions were excluded from investigations using this technique. Investigations from several labs have now demonstrated that extracellular proteins can be studied using two-hybrid methods, thereby enabling intense study of extracellular protein partners using the robust nature and the genetic power of yeast.
引用
收藏
页码:302 / 311
页数:10
相关论文
共 106 条
[1]   YEAST ARGININE PERMEASE - NUCLEOTIDE-SEQUENCE OF THE CAN1 GENE [J].
AHMAD, M ;
BUSSEY, H .
CURRENT GENETICS, 1986, 10 (08) :587-592
[2]   A protein linkage map of Escherichia coli bacteriophage T7 [J].
Bartel, PL ;
Roecklein, JA ;
SenGupta, D ;
Fields, S .
NATURE GENETICS, 1996, 12 (01) :72-77
[3]   STEROID-HORMONE RECEPTORS - MANY ACTORS IN SEARCH OF A PLOT [J].
BEATO, M ;
HERRLICH, P ;
SCHUTZ, G .
CELL, 1995, 83 (06) :851-857
[4]  
BEMIS LT, 1995, METHOD CELL BIOL, V46, P139
[5]   Getting more from the two-hybrid system: N-terminal fusions to LexA are efficient and sensitive baits for two-hybrid studies [J].
Beranger, F ;
Aresta, S ;
deGunzburg, J ;
Camonis, J .
NUCLEIC ACIDS RESEARCH, 1997, 25 (10) :2035-2036
[6]   A EUKARYOTIC TRANSCRIPTIONAL ACTIVATOR BEARING THE DNA SPECIFICITY OF A PROKARYOTIC REPRESSOR [J].
BRENT, R ;
PTASHNE, M .
CELL, 1985, 43 (03) :729-736
[7]  
Broach JR, 1996, NATURE, V384, P14
[8]   Vectors for expressing proteins at the amino-terminus of an activation domain for use in the yeast two-hybrid system [J].
Brown, MA ;
MacGillivray, RTA .
ANALYTICAL BIOCHEMISTRY, 1997, 247 (02) :451-452
[9]   Use of the yeast one-hybrid system to screen for mutations in the ligand-binding domain of the estrogen receptor [J].
Bush, SM ;
Folta, S ;
Lanningan, DA .
STEROIDS, 1996, 61 (03) :102-109
[10]  
Butt TR, 1996, GENE EXPRESSION, V5, P255