Optimizing low-light microscopy with back-illuminated electron multiplying charge-coupled device: enhanced sensitivity, speed, and resolution

被引:42
作者
Coates, CG
Denvir, DJ
McHale, NG
Thornbury, KD
Hollywood, MA
机构
[1] Andor Technol Ltd, Belfast BT12 7AL, Antrim, North Ireland
[2] Queens Univ Belfast, Ctr Med Biol, Smooth Muscle Grp, Belfast BT9 7BL, Antrim, North Ireland
基金
英国惠康基金; 英国医学研究理事会;
关键词
charge-coupled device; electron multiplying charge-coupled device; intensified charge-coupled device; calcium flux microscopy; intracellular ion signalling; back-illuminated charge-coupled device; single photon sensitivity; single molecule detection; quantum efficiency; impact ionization;
D O I
10.1117/1.1805559
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The back-illuminated electron multiplying charge-coupled device (EMCCD) camera is having a profound influence on the field of low-light dynamic cellular microscopy, combining highest possible photon collection efficiency with the ability to virtually eliminate the readout noise detection limit. We report here the use of this camera, in 512X512 frame-transfer chip format at 10-MHz pixel readout speed, in optimizing a demanding ultra-low-light intracellular calcium flux microscopy setup. The arrangement employed includes a spinning confocal Nipkow disk, which, while facilitating the need to both generate images at very rapid frame rates and minimize background photons, yields very weak signals. The challenge for the camera lies not just in detecting as many of these scarce photons as possible, but also in operating at a frame rate that meets the temporal resolution requirements of many low-light microscopy approaches, a particular demand of smooth muscle calcium flux microscopy. Results presented illustrate both the significant sensitivity improvement offered by this technology over the previous standard in ultra-low-light CCD detection, the Gen 111+intensified charge-coupled device (ICCD), and also portray the advanced temporal and spatial resolution capabilities of the EMCCD. (C) 2004 Society of Photo-Optical Instrumentation Engineers.
引用
收藏
页码:1244 / 1252
页数:9
相关论文
共 16 条
[1]   Probing single molecules in single living cells [J].
Byassee, TA ;
Chan, WCW ;
Nie, SM .
ANALYTICAL CHEMISTRY, 2000, 72 (22) :5606-5611
[2]  
COATES CG, BACK ILLUMINATED ELE
[3]   Electron multiplying CCD technology: The new ICCD [J].
Denvir, DJ ;
Conroy, E .
LOW-LIGHT-LEVEL AND REAL-TIME IMAGING SYSTEMS, COMPONENTS, AND APPLICATIONS, 2003, 4796 :164-174
[4]   Electron multiplying CCD technology: Application to ultrasensitive detection of biomolecules [J].
Denvir, DJ ;
Coates, CG .
BIOMEDICAL NANOTECHNOLOGY ARCHITECTURES AND APPLICATIONS, 2002, 4626 :502-512
[5]   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
[6]  
HARRIS EJ, EVALUATION NOVEL CCD
[7]   Voltage dependence of the coupling of Ca2+ sparks to BKCa channels in urinary bladder smooth muscle [J].
Herrera, GM ;
Heppner, TJ ;
Nelson, MT .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2001, 280 (03) :C481-C490
[8]  
HOLLYWOOD MA, 2003, J PHYSL LONDON P, V548, P16
[9]   Calcium sparks in smooth muscle [J].
Jaggar, JH ;
Porter, VA ;
Lederer, WJ ;
Nelson, MT .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2000, 278 (02) :C235-C256
[10]  
Janesick J. R., 2001, SCI CHARGE COUPLED D