TY - JOUR
T1 - Import of firefly luciferase into peroxisomes of permeabilized Chinese hamster ovary cells
T2 - A model system to study peroxisomal protein import in vitro
AU - Rapp, S.
AU - Soto, U.
AU - Just, W. W.
N1 - A model system for the study of in vitro peroxisomal protein import is described. Chinese hamster ovary (CHO) cells were permeabilized by the bacteria...
PY - 1993/3
Y1 - 1993/3
N2 - A model system for the study of in vitro peroxisomal protein import is described. Chinese hamster ovary (CHO) cells were permeabilized by the bacterial toxin streptolysin O (SLO) and their peroxisomes thus became accessible for a model import protein. Firefly luciferase (FL), which was previously shown to be imported into mammalian peroxisomes in vivo, was used as the reporter protein. When SLO-permeabilized CHO cells were incubated with FL in the presence of an ATP-regenerating system, import of FL could be documented by immunofluorescence staining of the cells with monospecific anti-FL antiserum. FL import increased with time and was dependent on temperature and the presence of hydrolysable ATP, which could not be replaced by GTP. The model system functioned reproducibly and should be of use for investigating fundamental questions on the mechanism of peroxisomal proteinimport.
AB - A model system for the study of in vitro peroxisomal protein import is described. Chinese hamster ovary (CHO) cells were permeabilized by the bacterial toxin streptolysin O (SLO) and their peroxisomes thus became accessible for a model import protein. Firefly luciferase (FL), which was previously shown to be imported into mammalian peroxisomes in vivo, was used as the reporter protein. When SLO-permeabilized CHO cells were incubated with FL in the presence of an ATP-regenerating system, import of FL could be documented by immunofluorescence staining of the cells with monospecific anti-FL antiserum. FL import increased with time and was dependent on temperature and the presence of hydrolysable ATP, which could not be replaced by GTP. The model system functioned reproducibly and should be of use for investigating fundamental questions on the mechanism of peroxisomal proteinimport.
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U2 - 10.1006/excr.1993.1058
DO - 10.1006/excr.1993.1058
M3 - Article
C2 - 8453998
SN - 0014-4827
VL - 205
SP - 59
EP - 65
JO - Experimental Cell Research
JF - Experimental Cell Research
IS - 1
ER -