共 34 条
Pin-Hole Array Correlation Imaging: Highly Parallel Fluorescence Correlation Spectroscopy
被引:32
作者:

Needleman, Daniel J.
论文数: 0 引用数: 0
h-index: 0
机构:
Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA

Xu, Yangqing
论文数: 0 引用数: 0
h-index: 0
机构:
Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA

Mitchison, Timothy J.
论文数: 0 引用数: 0
h-index: 0
机构:
Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
机构:
[1] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
关键词:
CROSS-CORRELATION SPECTROSCOPY;
LASER-SCANNING MICROSCOPE;
DISK CONFOCAL MICROSCOPE;
COUPLED-DEVICE CAMERA;
LIVING CELLS;
STATISTICAL ACCURACY;
DYNAMICS;
TRANSPORT;
EXCITATION;
NUMBER;
D O I:
10.1016/j.bpj.2009.03.023
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
In this work, we describe pin-hole array correlation imaging, a multipoint version of fluorescence correlation spectroscopy, based upon a stationary Nipkow disk and a high-speed electron multiplying charged coupled detector. We characterize the system and test its performance on a variety of samples, including 40 nm colloids, a fluorescent protein complex, a membrane dye, and a fluorescence fusion protein. Our results demonstrate that pin-hole array correlation imaging is capable of simultaneously performing tens or hundreds of fluorescence correlation spectroscopy-style measurements in cells, with sufficient sensitivity and temporal resolution to study the behaviors of membrane-bound and soluble molecules labeled with conventional chemical dyes or fluorescent proteins.
引用
收藏
页码:5050 / 5059
页数:10
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