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Analysis of Active Transport by Fluorescence Recovery after Photobleaching.

Publication ,  Journal Article
Ciocanel, M-V; Kreiling, JA; Gagnon, JA; Mowry, KL; Sandstede, B
Published in: Biophysical journal
April 2017

Fluorescence recovery after photobleaching (FRAP) is a well-established experimental technique to study binding and diffusion of molecules in cells. Although a large number of analytical and numerical models have been developed to extract binding and diffusion rates from FRAP recovery curves, active transport of molecules is typically not included in the existing models that are used to estimate these rates. Here we present a validated numerical method for estimating diffusion, binding/unbinding rates, and active transport velocities using FRAP data that captures intracellular dynamics through partial differential equation models. We apply these methods to transport and localization of mRNA molecules in Xenopus laevis oocytes, where active transport processes are essential to generate developmental polarity. By providing estimates of the effective velocities and diffusion, as well as expected run times and lengths, this approach can help quantify dynamical properties of localizing and nonlocalizing RNA. Our results confirm the distinct transport dynamics in different regions of the cytoplasm, and suggest that RNA movement in both the animal and vegetal directions may influence the timescale of RNA localization in Xenopus oocytes. We also show that model initial conditions extracted from FRAP postbleach intensities prevent underestimation of diffusion, which can arise from the instantaneous bleaching assumption. The numerical and modeling approach presented here to estimate parameters using FRAP recovery data is a broadly applicable tool for systems where intracellular transport is a key molecular mechanism.

Duke Scholars

Published In

Biophysical journal

DOI

EISSN

1542-0086

ISSN

0006-3495

Publication Date

April 2017

Volume

112

Issue

8

Start / End Page

1714 / 1725

Related Subject Headings

  • Xenopus laevis
  • Red Fluorescent Protein
  • RNA, Messenger
  • Protein Binding
  • Oocytes
  • Motion
  • Models, Molecular
  • Microinjections
  • Luminescent Proteins
  • Levivirus
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Ciocanel, M.-V., Kreiling, J. A., Gagnon, J. A., Mowry, K. L., & Sandstede, B. (2017). Analysis of Active Transport by Fluorescence Recovery after Photobleaching. Biophysical Journal, 112(8), 1714–1725. https://doi.org/10.1016/j.bpj.2017.02.042
Ciocanel, Maria-Veronica, Jill A. Kreiling, James A. Gagnon, Kimberly L. Mowry, and Björn Sandstede. “Analysis of Active Transport by Fluorescence Recovery after Photobleaching.Biophysical Journal 112, no. 8 (April 2017): 1714–25. https://doi.org/10.1016/j.bpj.2017.02.042.
Ciocanel M-V, Kreiling JA, Gagnon JA, Mowry KL, Sandstede B. Analysis of Active Transport by Fluorescence Recovery after Photobleaching. Biophysical journal. 2017 Apr;112(8):1714–25.
Ciocanel, Maria-Veronica, et al. “Analysis of Active Transport by Fluorescence Recovery after Photobleaching.Biophysical Journal, vol. 112, no. 8, Apr. 2017, pp. 1714–25. Epmc, doi:10.1016/j.bpj.2017.02.042.
Ciocanel M-V, Kreiling JA, Gagnon JA, Mowry KL, Sandstede B. Analysis of Active Transport by Fluorescence Recovery after Photobleaching. Biophysical journal. 2017 Apr;112(8):1714–1725.
Journal cover image

Published In

Biophysical journal

DOI

EISSN

1542-0086

ISSN

0006-3495

Publication Date

April 2017

Volume

112

Issue

8

Start / End Page

1714 / 1725

Related Subject Headings

  • Xenopus laevis
  • Red Fluorescent Protein
  • RNA, Messenger
  • Protein Binding
  • Oocytes
  • Motion
  • Models, Molecular
  • Microinjections
  • Luminescent Proteins
  • Levivirus