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.