Divalent cations can induce the exposure of GroEL hydrophobic surfaces and strengthen GroEL hydrophobic binding interactions -: Novel effects of Zn2+ GroEL interactions

被引:38
作者
Brazil, BT [1 ]
Ybarra, J [1 ]
Horowitz, PM [1 ]
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Biochem, San Antonio, TX 78284 USA
关键词
D O I
10.1074/jbc.273.6.3257
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
Fluorescent and non-fluorescent probes have been used to show that divalent cations (Ca2+, Mg2+, Mn2+, and Zn2+) significantly increase hydrophobic exposure on GroEL, whereas monovalent cations (K+ and Na+) have little effect, Zn2+ always induced the largest amount of hydrophobic exposure on GroEL, By using a new method based on interactions of GroEL with octyl-Sepharose, it was demonstrated that Zn2+ binding strengthens GroEL hydrophobic binding interactions and increases the efficiency of substrate release upon the addition of MgATP and GroES. The binding of 4,4'-bis(1-anilino-8-naphthalenesulfonic acid) to GroEL in the presence of Zn2+ has a K-d congruent to 1 mu M, which is similar to that observed previously for the GroEL 4,4'-bis(1-anilino-8-naphthalenesulfonic acid) complex, Urea denaturation, sedimentation velocity ultracentrifugation, and electron microscopy revealed that the quaternary structure of GroEL in the presence of Zn2+ had a stability and morphology equivalent to unliganded GroEL. In contrast, circular dichroism suggested some loss in both alpha-helical and beta-sheet secondary structure in the presence of Zn2+. These data suggest that divalent cations can modulate the amount of hydrophobic surface presented by GroEL, Furthermore, the influence of Zn2+ on GroEL hydrophobic surface exposure as well as substrate binding and release appears to be distinct from the stabilizing effects of Mg2+ on GroEL quaternary structure.
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页码:3257 / 3263
页数:7
相关论文
共 26 条
[1]   EVALUATION OF SECONDARY STRUCTURE OF PROTEINS FROM UV CIRCULAR-DICHROISM SPECTRA USING AN UNSUPERVISED LEARNING NEURAL-NETWORK [J].
ANDRADE, MA ;
CHACON, P ;
MERELO, JJ ;
MORAN, F .
PROTEIN ENGINEERING, 1993, 6 (04) :383-390
[2]   PRINCIPLES THAT GOVERN FOLDING OF PROTEIN CHAINS [J].
ANFINSEN, CB .
SCIENCE, 1973, 181 (4096) :223-230
[3]   EFFECT OF DIVALENT-CATIONS ON THE MOLECULAR-STRUCTURE OF THE GROEL OLIGOMER [J].
AZEM, A ;
DIAMANT, S ;
GOLOUBINOFF, P .
BIOCHEMISTRY, 1994, 33 (21) :6671-6675
[4]   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
[5]   Model peptide studies demonstrate that amphipathic secondary structures can be recognized by the chaperonin GroEL (cpn60) [J].
Brazil, BT ;
Cleland, JL ;
McDowell, RS ;
Skelton, NJ ;
Paris, K ;
Horowitz, PM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (08) :5105-5111
[6]   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
[7]   MOLECULAR CHAPERONES [J].
ELLIS, RJ ;
VANDERVIES, SM .
ANNUAL REVIEW OF BIOCHEMISTRY, 1991, 60 :321-347
[8]   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
[9]   PROMOTION OF THE INVITRO RENATURATION OF DODECAMERIC GLUTAMINE-SYNTHETASE FROM ESCHERICHIA-COLI IN THE PRESENCE OF GROEL (CHAPERONIN-60) AND ATP [J].
FISHER, MT .
BIOCHEMISTRY, 1992, 31 (16) :3955-3963
[10]   INDIVIDUAL SUBUNITS OF BACTERIAL LUCIFERASE ARE MOLTEN GLOBULES AND INTERACT WITH MOLECULAR CHAPERONES [J].
FLYNN, GC ;
BECKERS, CJM ;
BAASE, WA ;
DAHLQUIST, FW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (22) :10826-10830