Diffusion of green fluorescent protein in the aqueous-phase lumen of endoplasmic reticulum

Citation
Mj. Dayel et al., Diffusion of green fluorescent protein in the aqueous-phase lumen of endoplasmic reticulum, BIOPHYS J, 76(5), 1999, pp. 2843-2851
Citations number
45
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOPHYSICAL JOURNAL
ISSN journal
00063495 → ACNP
Volume
76
Issue
5
Year of publication
1999
Pages
2843 - 2851
Database
ISI
SICI code
0006-3495(199905)76:5<2843:DOGFPI>2.0.ZU;2-4
Abstract
The endoplasmic reticulum (ER) is the major compartment for the processing and quality control of newly synthesized proteins. Green fluorescent protei n (GFP) was used as a noninvasive probe to determine the Viscous properties of the aqueous lumen of the ER, GFP was targeted to the ER lumen of CHO ce lls by transient transfection with cDNA encoding GFP (S65T/F64L mutant) wit h a C-terminus KDEL retention sequence and upstream prolactin secretory seq uence. Repeated laser illumination of a fixed 2-mu m diameter spot resulted in complete bleaching of ER-associated GFP throughout the cell, indicating a continuous ER lumen. A residual amount (<1 %) of GFP-KDEL was perinuclea r and noncontiguous with the ER, presumably within a pre- or cis-Golgi comp artment involved in KDEL-substrate retention. Quantitative spot photobleach ing with a single brief bleach pulse indicated that GFP was fully mobile wi th a t(1/2) for fluorescence recovery of 88 +/- 5 ms (SE; 60x lens) and 143 +/- 8 ms (40X). Fluorescence recovery was abolished by paraformaldehyde ex cept for a small component of reversible photobleaching with t(1/2) of 3 ms . For comparison, the t(1/2) for photobleaching of GFP in cytoplasm was 14 +/- 2 ms (60x) and 24 +/- I ms (40X). Utilizing a mathematical model that a ccounted for ER reticular geometry, a GFP diffusion coefficient of 0.5-1 x 10(-7) cm(2)/s was computed, 9-18-fold less than that in water and 3-6-fold less than that in cytoplasm. By frequency-domain microfluorimetry, the GFP rotational correlation time was measured to be 39 +/- 8 ns, similar to 2-f old greater than that in water but comparable to that in the cytoplasm. Flu orescence recovery after photobleaching using a 40X lens was measured (at 2 3 degrees C unless otherwise indicated) for several potential effecters of ER structure and/or lumen environment: t(1/2) values (in ms) were 143 +/- 8 (control), 100 +/- 13 (37 degrees C), 53 +/- 13 (brefeldin A), and 139 +/- 6 (dithiothreitol). These results indicate moderately slowed GFP diffusion in a continuous ER lumen.