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
[41]   Design and characterization of a DNA-encoded, voltage-sensitive fluorescent protein [J].
Sakai, R ;
Repunte-Canonigo, V ;
Raj, CD ;
Knöpfel, T .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2001, 13 (12) :2314-2318
[42]   Activation of Shaker potassium channels I.: Characterization of voltage-dependent transitions [J].
Schoppa, NE ;
Sigworth, FJ .
JOURNAL OF GENERAL PHYSIOLOGY, 1998, 111 (02) :271-294
[43]   Fluorescence correlation spectroscopy reveals fast optical excitation-driven intramolecular dynamics of yellow fluorescent proteins [J].
Schwille, P ;
Kummer, S ;
Heikal, AA ;
Moerner, WE ;
Webb, WW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (01) :151-156
[44]   A genetically encoded optical probe of membrane voltage [J].
Siegel, MS ;
Isacoff, EY .
NEURON, 1997, 19 (04) :735-741
[45]   The green fluorescent protein [J].
Tsien, RY .
ANNUAL REVIEW OF BIOCHEMISTRY, 1998, 67 :509-544
[46]  
TYTGAT J, 1993, J BIOL CHEM, V268, P23777
[47]   One- and two-photon excited fluorescence lifetimes and anisotropy decays of Green Fluorescent Proteins [J].
Volkmer, A ;
Subramaniam, V ;
Birch, DJS ;
Jovin, TM .
BIOPHYSICAL JOURNAL, 2000, 78 (03) :1589-1598
[48]   Structural basis of spectral shifts in the yellow-emission variants of green fluorescent protein [J].
Wachter, RM ;
Elsliger, MA ;
Kallio, K ;
Hanson, GT ;
Remington, SJ .
STRUCTURE, 1998, 6 (10) :1267-1277
[49]   Shedding light on the dark and weakly fluorescent states of green fluorescent proteins [J].
Weber, W ;
Helms, V ;
McCammon, JA ;
Langhoff, PW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (11) :6177-6182
[50]   How does the W434F mutation block current in Shaker potassium channels? [J].
Yang, YS ;
Yan, YY ;
Sigworth, FJ .
JOURNAL OF GENERAL PHYSIOLOGY, 1997, 109 (06) :779-789