Comparison of the reaction progress of calcineurin with Mn2+ and Mg2+

被引:20
作者
Martin, BL
Jurado, LA
Hengge, AC
机构
[1] Univ Tennessee, Dept Biochem, Memphis, TN 38163 USA
[2] Univ Wisconsin, Inst Enzyme Res, Madison, WI 53705 USA
关键词
D O I
10.1021/bi981748l
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
Activation of calcineurin by Mn2+ and Mg2+ was compared using a heavy atom isotope analogue of the substrate p-nitrophenyl phosphate (pNPP), Heavy atom isotope effects were measured for Mg2+ activation and compared to published results of the isotope effects with Mn2+ as the activating metal. Isotope effects were measured for the kinetic parameter V-max/K-m at the nonbridging oxygen atoms [(18)(V/K)(nonbridge)]; at the position of bond cleavage in the bridging oxygen atom [(18)(V/K)(bridge)]; and at the nitrogen atom in the nitrophenol leaving group [(15)(V/K)]. The isotope effects increased in magnitude upon changing from an optimal pH to a nonoptimal pH; the (18)(V/K)(bridge) effect increased from 1.0154 (+/-0.0007) to 1.0198 (+/-0.0002), and the (15)(V/K) effect: increased from 1.0018 (+/-0.0002) to 1.0021 (+/-0.0003). The value for (18)(V/K)(nonbridge) is 0.9910 (+/-0.0003) at pH 7.0. As with Mn2+, the (18)(V/K)(nonbridge) isotope effect indicated that the dianion was the substrate for catalysis, and that a dissociative transition state was operative for the phosphoryl transfer. Comparison to results for Mn2+ activation suggested that chemistry was more rate-limiting with Mg2+ than with Mn2+. Changing the activating metal concentration showed opposite trends with increasing Mg2+ increasing the commitment factor and seemingly making the chemistry less rate-limiting. The influence of viscosity was evaluated as well to gauge the role of chemistry. The activation of calcineurin-catalyzed hydrolysis of pNPP(1) by Mg2+ or Mn2+ at pH 7.0 was compared in the presence of viscogens, glycerol and poly(ethylene glycol). Increasing glycerol caused different effects with the two activators. With Mn2+ as the activator, calcineurin activity showed a normal response with k(cat) and k(cat)/K-m decreasing with viscosity. There was an inverse response with Mg2+ as the activator as values of k(cat)/K-m increased with viscosity. From values of the normalized k(cat)/K-m with Mn2+, the chemistry was found to be partially rate-limiting, consistent with previous heavy atom isotope studies (22). The effect observed for Mg2+ seems consistent with a change in the rate-limiting step for the two different metals at pH 7.0.
引用
收藏
页码:3386 / 3392
页数:7
相关论文
共 44 条
[1]   MAPPING THE TRANSITION-STATE FOR ATP HYDROLYSIS - IMPLICATIONS FOR ENZYMATIC CATALYSIS [J].
ADMIRAAL, SJ ;
HERSCHLAG, D .
CHEMISTRY & BIOLOGY, 1995, 2 (11) :729-739
[2]   CONSERVATION ANALYSIS AND STRUCTURE PREDICTION OF THE PROTEIN SERINE/THREONINE PHOSPHATASES - SEQUENCE SIMILARITY WITH DIADENOSINE TETRAPHOSPHATASE FROM ESCHERICHIA-COLI SUGGESTS HOMOLOGY TO THE PROTEIN PHOSPHATASES [J].
BARTON, GJ ;
COHEN, PTW ;
BARFORD, D .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 220 (01) :225-237
[3]   TRIOSEPHOSPHATE ISOMERASE CATALYSIS IS DIFFUSION CONTROLLED - APPENDIX - ANALYSIS OF TRIOSE PHOSPHATE EQUILIBRIA IN AQUEOUS-SOLUTION BY P-31 NMR [J].
BLACKLOW, SC ;
RAINES, RT ;
LIM, WA ;
ZAMORE, PD ;
KNOWLES, JR .
BIOCHEMISTRY, 1988, 27 (04) :1158-1167
[4]  
BOURNE N, 1984, J ORG CHEM, V49, P1200, DOI 10.1021/jo00181a011
[5]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[6]   INVESTIGATION OF DIFFUSION-LIMITED RATES OF CHYMOTRYPSIN REACTIONS BY VISCOSITY VARIATION [J].
BROUWER, AC ;
KIRSCH, JF .
BIOCHEMISTRY, 1982, 21 (06) :1302-1307
[7]   TRANSITION-STATE STRUCTURES FOR ENZYMATIC AND ALKALINE PHOSPHOTRIESTER HYDROLYSIS [J].
CALDWELL, SR ;
RAUSHEL, FM ;
WEISS, PM ;
CLELAND, WW .
BIOCHEMISTRY, 1991, 30 (30) :7444-7450
[8]   THE USE OF ISOTOPE EFFECTS IN THE DETAILED ANALYSIS OF CATALYTIC MECHANISMS OF ENZYMES [J].
CLELAND, WW .
BIOORGANIC CHEMISTRY, 1987, 15 (03) :283-302
[9]   PROTEIN SERINE THREONINE PHOSPHATASES - AN EXPANDING FAMILY [J].
COHEN, PTW ;
BREWIS, ND ;
HUGHES, V ;
MANN, DJ .
FEBS LETTERS, 1990, 268 (02) :355-359
[10]  
COOK PF, 1991, ENZYME MECHANISM ISO