A high sensitivity time-resolved microfluorimeter for real-time cell biology

被引:8
|
作者
MartinFernandez, ML
Tobin, MJ
Clarke, DT
Gregory, CM
Jones, GR
机构
[1] CCLRC Daresbury Laboratory
来源
REVIEW OF SCIENTIFIC INSTRUMENTS | 1996年 / 67卷 / 10期
关键词
D O I
10.1063/1.1147138
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
We describe an instrument based on the novel combination of synchrotron radiation, a high sensitivity time-resolved microfluorimeter, and a multiframe single photon counting data acquisition system. This instrument has been designed specifically to measure kinetic events in live cells using fluorescence resonance energy transfer, and is capable of rapidly collecting multiple consecutive decay profiles from a small number of fluorophores. The low irradiance on the samples (< 10 mW/cm(2)) greatly reduces probe photobleaching and specimen photodamage during prolonged exposures. The Daresbury Synchrotron Radiation Source provides fully wavelength tunable light pulses that have a full width half-maximum of 160 ps at a repetition rate of 3.125 MHz, with the high temporal stability required for continuous measurements over periods of hours. A very low limit of detection (< 10(4) molecules/mW/cm(2)) is accomplished by combining a high-gain single photon counting detection system with a low fluorescence background optical layout. The latter is achieved by the inclusion of collimating optics, a reflecting objective, and a specially designed beam stop situated in the epi-fluorescence light-path. A typical irradiance of 8 mW/cm(2) on a sample of similar to 10(5) fluorescein molecules gives, in under 20 a, a fluorescence decay profile with a peak height of 10(4) counts, over 400 channels, and a signal to background ratio better than 40. The data acquisition system has been developed to have a real-time time-resolved fluorescence collection capability (denoted as TR(2)) so that fluorescence lifetime data can be continually collected throughout a changing process. To illustrate the potential of this instrument, we present the results of a TR(2) experiment in which lifetime measurements of fluorescence resonance energy transfer are used to monitor the degree of clustering of epidermal growth factor receptors during endocytosis, over a period of about 1 h, with a 5 s resolution. (C) 1996 American Institute of Physics.
引用
收藏
页码:3716 / 3721
页数:6
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