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Crystallization and preliminary X‐ray investigation of the Escherichia coli molecular chaperone cpn60 (GroEL)
Author(s) -
Spangfort Michael D.,
Surin Brian P.,
Oppentocht Jantina E.,
Weibull Claes,
Carlemalm Eric,
Dixon Nicholas E.,
Svensson L.Anders
Publication year - 1993
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/0014-5793(93)80083-7
Subject(s) - groel , escherichia coli , chaperone (clinical) , crystallization , escherichia coli proteins , microbiology and biotechnology , biology , chemistry , biochemistry , gene , medicine , organic chemistry , pathology
The Escherichia coli molecular chaperone, cpn60 (GroEL), has been purified from an overproducing E. coli strain and crystallized. Of the two crystal forms that were obtained, one was found to be suitable for crystallographic and structural studies at low resolution. Preliminary X‐ray investigation of the crystals show unit cell dimensions: a = 143.3, b = 154.6 and c = 265 Å, with α = 82°, β = 95° and γ = 107°. The space group is P1 and the crystals diffract to a maximum of 7 Å when using CuK α X‐rays from a rotating anode. Both electron microscopy and non‐denaturing electrophoretic analysis of redissolved cpn60 crystals show that cpn60 crystallizes in the native oligomeric form. Comparison between the dimensions of oligomeric cpn60 and the crystallographic unit cell volume suggests that the unit cell contains two oligomeric cpn60 molecules. The V M value for two cpn60 molecules per unit cell is 3.5 Å 3 /Da, corresponding to a water content of 65%. Electrophoretic analysis under denaturing conditions shows that the cpn60 in crystals is heterogeneous, and this probably explains the limited resolution of the diffraction data.