We have established efficient translocation of newly synthesized prote
ins into the endoplasmic reticulum of permeabilized Mel Juso cells, By
site-specific photo-crosslinking we show that translocating polypepti
de chains contact the same components of permeabilized cells ER as in
dog pancreas rough microsomes, This cellular assay system has the pote
ntial to overcome the limitations of isolated microsomes in investigat
ing the molecular environment of a newly synthesized protein after the
y have left the ER translocation site.