Advanced Technologies for Studies on Protein Interactomes

被引:24
作者
Guan, Hongtao [1 ]
Kiss-Toth, Endre [1 ]
机构
[1] Univ Sheffield, Royal Hallamshire Hosp, Cardiovasc Res Unit, Sheffield S10 2JF, S Yorkshire, England
来源
PROTEIN - PROTEIN INTERACTION | 2008年 / 110卷
关键词
cDNA library screening; Protein-protein interactions; Proteomics;
D O I
10.1007/10_2007_092
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
One of the key challenges of biology in the post-genomic era is to assign function to the many genes revealed by large-scale sequencing programmes, since only a small fraction of gene function can be directly inferred from the coding sequence. Identifying interactions between proteins is a substantial part in understanding their function. The main technologies for investigating protein-protein interactions and assigning functions to proteins include direct detection intermolecular interactions through protein microarray, yeast two-hybrid system, mass spectrometry fluorescent techniques to visualize protein complexes or pull-down assays, as well as technologies detecting functional interactions between genes, such as RNAi knock down or functional screening of cDNA libraries. Over recent years, considerable advances have been made in the above techniques. in this review, we discuss some recent developments and their impact on the gene function annotation.
引用
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页码:1 / 24
页数:24
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共 86 条
[41]   Helical β-peptide inhibitors of the p53-hDM2 interaction [J].
Kritzer, JA ;
Lear, JD ;
Hodsdon, ME ;
Schepartz, A .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (31) :9468-9469
[42]   Genome-wide RNAi identifies p53-dependent and -independent regulators of germ cell apoptosis in C-elegans [J].
Lettre, G ;
Kritikou, EA ;
Jaeggi, M ;
Calixto, A ;
Fraser, AG ;
Kamath, RS ;
Ahringer, J ;
Hengartner, MO .
CELL DEATH AND DIFFERENTIATION, 2004, 11 (11) :1198-1203
[43]   Vertebrate MicroRNA genes [J].
Lim, LP ;
Glasner, ME ;
Yekta, S ;
Burge, CB ;
Bartel, DP .
SCIENCE, 2003, 299 (5612) :1540-1540
[44]   Transgene-induced RNA interference as a tool for plant functional genomics [J].
McGinnis, K ;
Chandler, V ;
Cone, K ;
Kaeppler, H ;
Kaeppler, S ;
Kerschen, A ;
Pikaard, C ;
Richards, E ;
Sidorenko, L ;
Smith, T ;
Springer, N ;
Wulan, T .
RNA INTERFERENCE, 2005, 392 :1-24
[45]   Identifying DNA sequences recognized by a transcription factor using a bacterial one-hybrid system [J].
Meng, Xiangdong ;
Wolfe, Scot A. .
NATURE PROTOCOLS, 2006, 1 (01) :30-45
[46]   IKK-1 and IKK-2: Cytokine-activated I kappa B kinases essential for NF-kappa B activation [J].
Mercurio, F ;
Zhu, HY ;
Murray, BW ;
Shevchenko, A ;
Bennett, BL ;
Li, JW ;
Young, DB ;
Barbosa, M ;
Mann, M .
SCIENCE, 1997, 278 (5339) :860-866
[47]   Proteomics in living cells [J].
Michnick, SW .
DRUG DISCOVERY TODAY, 2004, 9 (06) :262-267
[48]   Protein fragment complementation strategies for biochemical network mapping [J].
Michnick, SW .
CURRENT OPINION IN BIOTECHNOLOGY, 2003, 14 (06) :610-617
[49]   IRAK (Pelle) family member IRAK-2 and MyD88 as proximal mediators of IL-1 signaling [J].
Muzio, M ;
Ni, J ;
Feng, P ;
Dixit, VM .
SCIENCE, 1997, 278 (5343) :1612-1615
[50]   INTRODUCTION OF A CHIMERIC CHALCONE SYNTHASE GENE INTO PETUNIA RESULTS IN REVERSIBLE CO-SUPPRESSION OF HOMOLOGOUS GENES IN TRANS [J].
NAPOLI, C ;
LEMIEUX, C ;
JORGENSEN, R .
PLANT CELL, 1990, 2 (04) :279-289