Ja. Mendoza et al., TETRADECAMERIC CHAPERONIN-60 CAN BE ASSEMBLED IN-VITRO FROM MONOMERS IN A PROCESS THAT IS ATP INDEPENDENT, Biochimica et biophysica acta. Protein structure and molecular enzymology, 1247(2), 1995, pp. 209-214
The present work shows that monomers of cpn60 (groEL) formed at 2.5 M
urea could be assembled to tetradecamers in a process that was indepen
dent of ATP. Reassembled cpn60 was able to assist the folding of urea
unfolded rhodanese. When cpn60 was incubated at urea concentrations hi
gher than 2.75 M, assembly of tetradecameric cpn60 did not occur after
dialysis, and the presence of ATP did not stimulate the assembly proc
ess. The cpn60 used here did not display the previously reported ATP-d
ependent self-assembly of cpn60 monomers that required a higher urea c
oncentration (4 M) for formation (Lissen et al. (1990) Nature 348, 339
-342). Assembly and disassembly of cpn60 tetradecamers were followed a
s a function of the urea concentration by ultracentrifugation and gel
electrophoresis in the presence of urea. The electrophoresis results d
emonstrate that there is rapid assembly of tetradecamers following pre
incubation and rapid removal of urea at concentrations lower than 2.5
M. Thus, previous methods monitored irreversible dissociation of cpn60
, and the present results indicate that the cpn60 assembly requirement
s for ATP are dependent on pretreatment conditions.