Development of an improved FRET imaging two-photon microscope combining lifetime and spectral imaging
被引:2
作者:
Pelet, S
论文数: 0引用数: 0
h-index: 0
机构:
MIT, Biol Engn Div, Cambridge, MA 02139 USAMIT, Biol Engn Div, Cambridge, MA 02139 USA
Pelet, S
[1
]
Previte, MJR
论文数: 0引用数: 0
h-index: 0
机构:
MIT, Biol Engn Div, Cambridge, MA 02139 USAMIT, Biol Engn Div, Cambridge, MA 02139 USA
Previte, MJR
[1
]
Kim, KH
论文数: 0引用数: 0
h-index: 0
机构:
MIT, Biol Engn Div, Cambridge, MA 02139 USAMIT, Biol Engn Div, Cambridge, MA 02139 USA
Kim, KH
[1
]
So, PTC
论文数: 0引用数: 0
h-index: 0
机构:
MIT, Biol Engn Div, Cambridge, MA 02139 USAMIT, Biol Engn Div, Cambridge, MA 02139 USA
So, PTC
[1
]
机构:
[1] MIT, Biol Engn Div, Cambridge, MA 02139 USA
来源:
MULTIPHOTON MICROSCOPY IN THE BIOMEDICAL SCIENCES IV
|
2004年
/
5323卷
关键词:
D O I:
10.1117/12.537620
中图分类号:
R318 [生物医学工程];
学科分类号:
0831 ;
摘要:
FRET imaging is widely used in biology to map protein interactions in living cells. A number of recent technical developments promise to provide more accurate and quantitative measurement FRET efficiencies and protein bonding ratio. Using a reference FRET construct based on a doubly labeled DNA, one can estimate the accuracy of different techniques like spectral or lifetime imaging to resolve FRET. Further improvement have lead to the possibility of measuring in a single detector both spectral and lifetime information from the fluorescence emitted by the sample. We are currently building such a system based on an intensity modulated multi-anode PMT and have developed a global fitting algorithm to extract valuable information from combined spectral and lifetime imaging data sets.