4.5 Article

Pin-Hole Array Correlation Imaging: Highly Parallel Fluorescence Correlation Spectroscopy

期刊

BIOPHYSICAL JOURNAL
卷 96, 期 12, 页码 5050-5059

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CELL PRESS
DOI: 10.1016/j.bpj.2009.03.023

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资金

  1. Life Sciences Research Foundation
  2. Novartis (Basel, Switzerland)

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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.

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