Genetically encoded optical sensors of neuronal activity and cellular function

被引:24
作者
Guerrero, G [1 ]
Isacoff, EY [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Phys Biosci Div, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
关键词
D O I
10.1016/S0959-4388(00)00256-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Fluorescent proteins (FPs) have been engineered to produce an optical report in response to cellular signals. FP fluorescence can be made directly sensitive to the chemical environment, via specific mutations of or around the chromophore. Alternatively, FPs can be made indirectly sensitive to cellular signals by their fusion to 'detector' proteins that respond to specific cellular signals with structural rearrangements that act on the FP to alter fluorescence. These optical sensors of membrane voltage, neurotransmitter release, and intracellular messengers, including powerful new sensors of Ca2+, cyclic nucleotides and nitric oxide, are likely to provide new insights into the workings of cellular signals and of information processing in neural circuits.
引用
收藏
页码:601 / 607
页数:7
相关论文
共 57 条
[1]   Cameleon calcium indicator reports cytoplasmic calcium dynamics in Arabidopsis guard cells [J].
Allen, GJ ;
Kwak, JM ;
Chu, SP ;
Llopis, J ;
Tsien, RY ;
Harper, JF ;
Schroeder, JI .
PLANT JOURNAL, 1999, 19 (06) :735-747
[2]   Biochemistry, mutagenesis, and oligomerization of DsRed, a red fluorescent protein from coral [J].
Baird, GS ;
Zacharias, DA ;
Tsien, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (22) :11984-11989
[3]   Circular permutation and receptor insertion within green fluorescent proteins [J].
Baird, GS ;
Zacharias, DA ;
Tsien, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (20) :11241-11246
[4]   Probing the ground state structure of the green fluorescent protein chromophore using Raman spectroscopy [J].
Bell, AF ;
He, X ;
Wachter, RM ;
Tonge, PJ .
BIOCHEMISTRY, 2000, 39 (15) :4423-4431
[5]   Structural basis for dual excitation and photoisomerization of the Aequorea victoria green fluorescent protein [J].
Brejc, K ;
Sixma, TK ;
Kitts, PA ;
Kain, SR ;
Tsien, RY ;
Ormo, M ;
Remington, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2306-2311
[6]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[7]   Ultra-fast excited state dynamics in green fluorescent protein: Multiple states and proton transfer [J].
Chattoraj, M ;
King, BA ;
Bublitz, GU ;
Boxer, SG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (16) :8362-8367
[8]   Photophysics and optical switching in green fluorescent protein mutants [J].
Creemers, TMH ;
Lock, AJ ;
Subramaniam, V ;
Jovin, TM ;
Völker, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :2974-2978
[9]   On/off blinking and switching behaviour of single molecules of green fluorescent protein [J].
Dickson, RM ;
Cubitt, AB ;
Tsien, RY ;
Moerner, WE .
NATURE, 1997, 388 (6640) :355-358
[10]   Structural and spectral response of green fluorescent protein variants to changes in pH [J].
Elsliger, MA ;
Wachter, RM ;
Hanson, GT ;
Kallio, K ;
Remington, SJ .
BIOCHEMISTRY, 1999, 38 (17) :5296-5301