Genetically encoded molecular probes to visualize and perturb signaling dynamics in living biological systems

被引:33
作者
Sample, Vedangi [1 ]
Mehta, Sohum [1 ]
Zhang, Jin [1 ,2 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Oncol, Baltimore, MD 21205 USA
关键词
Biosensors; FRET; Live cell imaging; Signaling; Targeted perturbations; GREEN FLUORESCENT PROTEIN; RESONANCE ENERGY-TRANSFER; IN-VIVO; SPATIOTEMPORAL CONTROL; OPTOGENETIC CONTROL; INDUCED PROXIMITY; CA2+ INDICATORS; RATIONAL DESIGN; OPTICAL CONTROL; CELLULAR CAMP;
D O I
10.1242/jcs.099994
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In this Commentary, we discuss two sets of genetically encoded molecular tools that have significantly enhanced our ability to observe and manipulate complex biochemical processes in their native context and that have been essential in deepening our molecular understanding of how intracellular signaling networks function. In particular, genetically encoded biosensors are widely used to directly visualize signaling events in living cells, and we highlight several examples of basic biosensor designs that have enabled researchers to capture the spatial and temporal dynamics of numerous signaling molecules, including second messengers and signaling enzymes, with remarkable detail. Similarly, we discuss a number of genetically encoded biochemical perturbation techniques that are being used to manipulate the activity of various signaling molecules with far greater spatial and temporal selectivity than can be achieved using standard pharmacological or genetic techniques, focusing specifically on examples of chemically driven and light-inducible perturbation strategies. We then describe recent efforts to combine these diverse and powerful molecular tools into a unified platform that can be used to elucidate the molecular details of biological processes that may potentially extend well beyond the realm of signal transduction.
引用
收藏
页码:1151 / 1160
页数:10
相关论文
共 113 条
[1]   Temporally precise in vivo control of intracellular signalling [J].
Airan, Raag D. ;
Thompson, Kimberly R. ;
Fenno, Lief E. ;
Bernstein, Hannah ;
Deisseroth, Karl .
NATURE, 2009, 458 (7241) :1025-1029
[2]   Genetically encoded calcium indicators for multi-color neural activity imaging and combination with optogenetics [J].
Akerboom, Jasper ;
Calderon, Nicole Carreras ;
Tian, Lin ;
Wabnig, Sebastian ;
Prigge, Matthias ;
Tolo, Johan ;
Gordus, Andrew ;
Orger, Michael B. ;
Severi, Kristen E. ;
Macklin, John J. ;
Patel, Ronak ;
Pulver, Stefan R. ;
Wardill, Trevor J. ;
Fischer, Elisabeth ;
Schueler, Christina ;
Chen, Tsai-Wen ;
Sarkisyan, Karen S. ;
Marvin, Jonathan S. ;
Bargmann, Cornelia I. ;
Kim, Douglas S. ;
Kugler, Sebastian ;
Lagnado, Leon ;
Hegemann, Peter ;
Gottschalk, Alexander ;
Schreiter, Eric R. ;
Looger, Loren L. .
FRONTIERS IN MOLECULAR NEUROSCIENCE, 2013, 6
[3]   Crystal Structures of the GCaMP Calcium Sensor Reveal the Mechanism of Fluorescence Signal Change and Aid Rational Design [J].
Akerboom, Jasper ;
Rivera, Jonathan D. Velez ;
Guilbe, Maria M. Rodriguez ;
Malave, Elisa C. Alfaro ;
Hernandez, Hector H. ;
Tian, Lin ;
Hires, S. Andrew ;
Marvin, Jonathan S. ;
Looger, Loren L. ;
Schreiter, Eric R. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (10) :6455-6464
[4]   Two-photon single-cell optogenetic control of neuronal activity by sculpted light [J].
Andrasfalvy, Bertalan K. ;
Zemelman, Boris V. ;
Tang, Jianyong ;
Vaziri, Alipasha .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (26) :11981-11986
[5]   Compartmentalized signalling: spatial regulation of cAMP by the action of compartmentalized phosphodiesterases [J].
Baillie, George S. .
FEBS JOURNAL, 2009, 276 (07) :1790-1799
[6]   Green light to illuminate signal transduction events [J].
Balla, Tamas .
TRENDS IN CELL BIOLOGY, 2009, 19 (11) :575-586
[7]  
Berg J, 2009, NAT METHODS, V6, P161, DOI [10.1038/NMETH.1288, 10.1038/nmeth.1288]
[8]  
BLOOM FE, 1973, PHARMACOL REV, V25, P343
[9]   Two-photon imaging of intratumoral CD8+ T cell cytotoxic activity during adoptive T cell therapy in mice [J].
Breart, Beatrice ;
Lemaitre, Fabrice ;
Celli, Susanna ;
Bousso, Philippe .
JOURNAL OF CLINICAL INVESTIGATION, 2008, 118 (04) :1390-1397
[10]   Protein scaffolds in MAP kinase signalling [J].
Brown, Matthew D. ;
Sacks, David B. .
CELLULAR SIGNALLING, 2009, 21 (04) :462-469