ELECTRON-MICROSCOPY OF THE GROEL-GROES FILAMENT

被引:9
作者
HARRIS, JR
ZAHN, R
PLUCKTHUN, A
机构
[1] MAX PLANCK INST BIOCHEM,W-8033 MARTINSRIED,GERMANY
[2] UNIV ZURICH,INST BIOCHEM,CH-8057 ZURICH,SWITZERLAND
关键词
D O I
10.1006/jsbi.1995.1031
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Electron microscopy of a filamentous complex of GroEL and GroES has been performed on negatively stained specimens. The filaments have been formed when GroEL and GroES at relatively low molar ratios (e.g., 1:1 to 1:3) are incubated at room temperature in the presence of magnesium and ATP. At higher molar ratio, the symmetrical GroEL-GroES complex predominates. Within the GroEL-GroES filaments, the same structural rearrangements of GroEL were observed as in the ''bulletshaped'' or symmetrical GroEL-GroES complexes. In the absence of GroES, GroEL molecules have no tendency to form linear filaments, The sharing of one GroES by two GroEL molecules might indicate a high plasticity of the GroEL-GroES complex. Preliminary Fourier analysis of filaments of increasing length indicates that they possess an inherent helicity. Using the negative staining-carbon film procedure, two-dimensional (2-D) crystal nucleation induced by ammonium molybdate-polyethylene glycol can create undulatory rows of side-on GroEL molecules, which are able extend as a p2 2-D crystal form, readily distinguishable from the filamentous GroEL-GroES aggregates. Crystallographic image processing indicates that the GroEL 2 x 7-mer itself possesses a dyad screw axis, in accord with existing higher resolution X-ray structure data. (C) 1995 Academic Press, Inc.
引用
收藏
页码:68 / 77
页数:10
相关论文
共 49 条
[1]   CHARACTERIZATION OF A FUNCTIONAL GROEL(14)(GROES(7))(2) CHAPERONIN HETERO-OLIGOMER [J].
AZEM, A ;
KESSEL, M ;
GOLOUBINOFF, P .
SCIENCE, 1994, 265 (5172) :653-656
[2]  
BEGAUER W, 1994, ZOOLOGY, V98, P51
[3]   THE CRYSTAL-STRUCTURE OF THE BACTERIAL CHAPERONIN GROEL AT 2.8-ANGSTROM [J].
BRAIG, K ;
OTWINOWSKI, Z ;
HEGDE, R ;
BOISVERT, DC ;
JOACHIMIAK, A ;
HORWICH, AL ;
SIGLER, PB .
NATURE, 1994, 371 (6498) :578-586
[4]   GROE FACILITATES REFOLDING OF CITRATE SYNTHASE BY SUPPRESSING AGGREGATION [J].
BUCHNER, J ;
SCHMIDT, M ;
FUCHS, M ;
JAENICKE, R ;
RUDOLPH, R ;
SCHMID, FX ;
KIEFHABER, T .
BIOCHEMISTRY, 1991, 30 (06) :1586-1591
[5]   LOCALIZATION OF THE BINDING-SITE OF AN ANTIBODY AFFECTING ATPASE ACTIVITY OF CHAPERONIN CPN60 FROM BORDETELLA-PERTUSSIS [J].
CEJKA, Z ;
GOULDKOSTKA, J ;
BURNS, D ;
KESSEL, M .
JOURNAL OF STRUCTURAL BIOLOGY, 1993, 111 (01) :34-38
[6]  
CHANDRASEKHAR GN, 1986, J BIOL CHEM, V261, P2414
[7]   LOCATION OF A FOLDING PROTEIN AND SHAPE CHANGES IN GROEL-GROES COMPLEXES IMAGED BY CRYOELECTRON MICROSCOPY [J].
CHEN, S ;
ROSEMAN, AM ;
HUNTER, AS ;
WOOD, SP ;
BURSTON, SG ;
RANSON, NA ;
CLARKE, AR ;
SAIBIL, HR .
NATURE, 1994, 371 (6494) :261-264
[8]  
COUTURETOSI E, 1986, EUR J CELL BIOL, V42, P359
[9]   RESIDUES IN CHAPERONIN GROEL REQUIRED FOR POLYPEPTIDE BINDING AND RELEASE [J].
FENTON, WA ;
KASHI, Y ;
FURTAK, K ;
HORWICH, AL .
NATURE, 1994, 371 (6498) :614-619
[10]  
FREY TG, 1978, 9TH P INT C EL MICR, V3, P107