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Identification of Fluorescent Compounds with Non-Specific Binding Property via High Throughput Live Cell Microscopy
PLOS ONE
  • Sangeeta Nath, Lawrence Berkeley National Laboratory
  • Virginia A. Spencer, Lawrence Berkeley National Laboratory
  • Ju Han, Lawrence Berkeley National Laboratory
  • Hang Chang, Lawrence Berkeley National Laboratory
  • Kai Zhang, Lawrence Berkeley National Laboratory
  • Gerald V. Fontenay, Lawrence Berkeley National Laboratory
  • Charles Anderson, University of California, Berkeley, California
  • Joel M. Hyman, Lawrence Berkeley National Laboratory
  • Marit Nilsen-Hamilton, Iowa State University
  • Young-Tae Chang, The National University of Singapore
  • Bahram Parvin, Lawrence Berkeley National Laboratory
Document Type
Article
Publication Version
Published Version
Publication Date
1-1-2012
DOI
10.1371/journal.pone.0028802
Abstract

Abstract Introduction

Compounds exhibiting low non-specific intracellular binding or non-stickiness are concomitant with rapid clearing and in high demand for live-cell imaging assays because they allow for intracellular receptor localization with a high signal/noise ratio. The non-stickiness property is particularly important for imaging intracellular receptors due to the equilibria involved. Method

Three mammalian cell lines with diverse genetic backgrounds were used to screen a combinatorial fluorescence library via high throughput live cell microscopy for potential ligands with high in- and out-flux properties. The binding properties of ligands identified from the first screen were subsequently validated on plant root hair. A correlative analysis was then performed between each ligand and its corresponding physiochemical and structural properties. Results

The non-stickiness property of each ligand was quantified as a function of the temporal uptake and retention on a cell-by-cell basis. Our data shows that (i) mammalian systems can serve as a pre-screening tool for complex plant species that are not amenable to high-throughput imaging; (ii) retention and spatial localization of chemical compounds vary within and between each cell line; and (iii) the structural similarities of compounds can infer their non-specific binding properties. Conclusion

We have validated a protocol for identifying chemical compounds with non-specific binding properties that is testable across diverse species. Further analysis reveals an overlap between the non-stickiness property and the structural similarity of compounds. The net result is a more robust screening assay for identifying desirable ligands that can be used to monitor intracellular localization. Several new applications of the screening protocol and results are also presented.

Comments

This is an article from PLOS ONE 7 (2012): 1, doi:10.1371/journal.pone.0028802. Posted with permission.

Rights
This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright Owner
Nath et al
Language
en
File Format
application/pdf
Citation Information
Sangeeta Nath, Virginia A. Spencer, Ju Han, Hang Chang, et al.. "Identification of Fluorescent Compounds with Non-Specific Binding Property via High Throughput Live Cell Microscopy" PLOS ONE Vol. 7 Iss. 1 (2012) p. 1 - 7
Available at: http://works.bepress.com/marit-nilsen-hamilton/21/