Imaging protein-protein interactions in living subjects

被引:9
作者
Paulmurugan, R
Ray, P
De, A
Chan, CT
Gambhir, SS
机构
[1] Stanford Univ, Sch Med, Dept Radiol, Mol Imaging Program,James H Clark Ctr, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, James Clark Ctr, Bio X Program, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
protein-protein interaction; non-invasive imaging; split-reporters; protein complementation; molecular imaging;
D O I
10.1016/j.trac.2005.02.005
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Only over the last three years methods have been developed to study protein-protein interactions occurring inside the intact cells within small living animals. This has been made possible by the explosion of non-invasive small-animal imaging technologies and the rapidly expanding field of molecular imaging, with technologies including bioluminescence imaging, fluorescence imaging, positron emission tomography (PET), and single photon emission computed tomography (SPECT). The first two techniques depend on light transmission through the animal, while the latter two depend on gamma ray transmission through the animal; in each case, the appropriate reporter genes or split-reporter genes are needed, along with the corresponding reporter probes. Other imaging technologies, such as magnetic resonance imaging (MRI) are also used for molecular imaging. but have not yet been validated specifically for imaging protein-protein interactions. The focus of this article is primarily on optical technologies for imaging protein-protein interactions. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:446 / 458
页数:13
相关论文
共 115 条
[11]   Optical imaging of Renilla luciferase reporter gene expression in living mice [J].
Bhaumik, S ;
Gambhir, SS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (01) :377-382
[12]   APPLICATION OF FLUORESCAMINE TO STUDY OF PROTEIN-DNA INTERACTIONS [J].
BODE, J ;
WILLMITZER, L .
NUCLEIC ACIDS RESEARCH, 1975, 2 (10) :1951-1965
[13]   Ceramide activates NFκB by inducing the processing of p105 [J].
Boland, MP ;
O'Neill, LAJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (25) :15494-15500
[14]  
Bollag D M, 1994, Methods Mol Biol, V36, P1
[15]   The use of resonance energy transfer in high-throughput screening: BRET versus FRET [J].
Boute, N ;
Jockers, R ;
Issad, T .
TRENDS IN PHARMACOLOGICAL SCIENCES, 2002, 23 (08) :351-354
[16]  
Boute N, 2001, MOL PHARMACOL, V60, P640
[17]   The Ras recruitment system, a novel approach to the study of protein-protein interactions [J].
Broder, YC ;
Katz, S ;
Aronheim, A .
CURRENT BIOLOGY, 1998, 8 (20) :1121-1124
[18]   A monomeric red fluorescent protein [J].
Campbell, RE ;
Tour, O ;
Palmer, AE ;
Steinbach, PA ;
Baird, GS ;
Zacharias, DA ;
Tsien, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (12) :7877-7882
[19]   Recognition between disordered states: Kinetics of the self-assembly of thioredoxin fragments [J].
Chaffotte, AF ;
Li, JH ;
Georgescu, RE ;
Goldberg, ME ;
Tasayco, ML .
BIOCHEMISTRY, 1997, 36 (51) :16040-16048
[20]  
Cherry S R, 2001, ILAR J, V42, P219