Tuning FlaSh: Redesign of the dynamics, voltage range, and color of the genetically encoded optical sensor of membrane potential

被引:74
作者
Guerrero, G [1 ]
Siegel, MS [1 ]
Roska, B [1 ]
Loots, E [1 ]
Isacoff, EY [1 ]
机构
[1] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
关键词
D O I
10.1016/S0006-3495(02)75361-7
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
The optical voltage sensor FlaSh, made from a fusion of a GFP "reporter domain" and a voltage-gated Shaker K+ channel "detector domain," has been mutagenically tuned in both the GFP reporter and channel detector domains. This has produced sensors with improved folding at 37degreesC, enabling use in mammalian preparations, and yielded variants with distinct spectra, kinetics, and voltage dependence, thus expanding the types of electrical signals that can be detected. The optical readout of FlaSh has also been expanded from single wavelength fluorescence intensity changes to dual wavelength measurements based on both voltage-dependent spectral shifts and changes in FRET. Different versions of FlaSh can now be chosen to optimize the detection of either action potentials or synaptic potentials, to follow high versus low rates of activity, and to best reflect electrical activity in cell types with distinct voltages of operation.
引用
收藏
页码:3607 / 3618
页数:12
相关论文
共 50 条
[31]   Fluorescent indicators for Ca2+ based on green fluorescent proteins and calmodulin [J].
Miyawaki, A ;
Llopis, J ;
Heim, R ;
McCaffery, JM ;
Adams, JA ;
Ikura, M ;
Tsien, RY .
NATURE, 1997, 388 (6645) :882-887
[32]   Red fluorescent protein from Discosoma as a fusion tag and a partner for fluorescence resonance energy transfer [J].
Mizuno, H ;
Sawano, A ;
Eli, P ;
Hama, H ;
Miyawaki, A .
BIOCHEMISTRY, 2001, 40 (08) :2502-2510
[33]   A fluorescent indicator for visualizing cAMP-induced phosphorylation in vivo [J].
Nagai, Y ;
Miyazaki, M ;
Aoki, R ;
Zama, T ;
Inouye, S ;
Hirose, K ;
Iino, M ;
Hagiwara, M .
NATURE BIOTECHNOLOGY, 2000, 18 (03) :313-316
[34]   Continual remodeling of postsynaptic density and its regulation by synaptic activity [J].
Okabe, S ;
Kim, HD ;
Miwa, A ;
Kuriu, T ;
Okado, H .
NATURE NEUROSCIENCE, 1999, 2 (09) :804-811
[35]  
Ormo M, 1996, SCIENCE, V273, P1392, DOI 10.1126/science.273.5280.1392
[36]   Use of the green fluorescent protein and its mutants in quantitative fluorescence microscopy [J].
Patterson, GH ;
Knobel, SM ;
Sharif, WD ;
Kain, SR ;
Piston, DW .
BIOPHYSICAL JOURNAL, 1997, 73 (05) :2782-2790
[37]   Role of metallothionein in nitric oxide signaling as revealed by a green fluorescent fusion protein [J].
Pearce, LL ;
Gandley, RE ;
Han, WP ;
Wasserloos, K ;
Stitt, M ;
Kanai, AJ ;
McLaughlin, MK ;
Pitt, BR ;
Levitan, ES .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (01) :477-482
[38]   GATING CURRENTS FROM A NONCONDUCTING MUTANT REVEAL OPEN-CLOSED CONFORMATIONS IN SHAKER K+ CHANNELS [J].
PEROZO, E ;
MACKINNON, R ;
BEZANILLA, F ;
STEFANI, E .
NEURON, 1993, 11 (02) :353-358
[39]   Detection in living cells of Ca2+-dependent changes in the fluorescence emission of an indicator composed of two green fluorescent protein variants linked by a calmodulin-binding sequence - A new class of fluorescent indicators [J].
Romoser, VA ;
Hinkle, PM ;
Persechini, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (20) :13270-13274
[40]  
Roska B, 1998, J NEUROSCI, V18, P3451