Fluorescence Recovery after Photobleaching and Single-Molecule Tracking Measurements
of Anisotropic Diffusion within Identical Regions of a Cylinder-Forming
Diblock Copolymer Film
posted on 2015-06-02, 00:00authored byKhanh-Hoa Tran-Ba, Daniel A. Higgins, Takashi Ito
This work demonstrates ensemble and
single-molecule diffusion measurements
within identical regions of a cylinder-forming polystyrene-poly(ethylene
oxide) diblock copolymer (PS-b-PEO) film using fluorescence
recovery after photobleaching (FRAP) and single-molecule tracking
(SMT). A PS-b-PEO film (∼4 μm thick)
with aligned cylindrical PEO microdomains containing 10 μM sulforhodamine
B (SRB) was prepared by directional solvent-vapor penetration (SVP)
of 1,4-dioxane. The ensemble diffusion behavior of SRB in the microdomains
was assessed in FRAP studies of circular photobleached regions (∼7
μm in diameter). The SRB concentration was subsequently reduced
by additional photobleaching, and the diffusion of individual SRB
molecules was explored using SMT in the identical area (∼16
× 16 μm2). The FRAP data showed anisotropic
fluorescence recovery, yielding the average microdomain orientation.
The extent of fluorescence recovery observed (∼90%) demonstrated
long-range microdomain connectivity, while the recovery time dependence
provided an ensemble measurement of the SRB diffusion coefficient
within the cylindrical microdomains. The SMT data exhibited one-dimensional
diffusion of individual SRB molecules along the SVP direction across
the entire film thickness, as consistent with the FRAP results. Importantly,
the average of the single-molecule diffusion coefficients was close
to the value obtained from FRAP in the identical area. In some cases,
SMT offered smaller diffusion coefficients than FRAP, possibly due
to contributions from SRB molecules confined within short PEO microdomains.
The implementation of FRAP and SMT measurements in identical areas
provides complementary information on molecular diffusion with minimal
influence of sample heterogeneity, permitting direct comparison of
ensemble and single-molecule diffusion behavior.