Literature DB >> 10079083

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

B L Martin1, L A Jurado, A C Hengge.   

Abstract

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 Vmax/Km 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 pNPP1 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 kcat and kcat/Km decreasing with viscosity. There was an inverse response with Mg2+ as the activator as values of kcat/Km increased with viscosity. From values of the normalized kcat/Km 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.

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Year:  1999        PMID: 10079083     DOI: 10.1021/bi981748l

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  4 in total

1.  A calcineurin docking motif (LXVP) in dynamin-related protein 1 contributes to mitochondrial fragmentation and ischemic neuronal injury.

Authors:  Andrew M Slupe; Ronald A Merrill; Kyle H Flippo; Mark A Lobas; Jon C D Houtman; Stefan Strack
Journal:  J Biol Chem       Date:  2013-03-13       Impact factor: 5.157

2.  Mechanistic study of protein phosphatase-1 (PP1), a catalytically promiscuous enzyme.

Authors:  Claire McWhirter; Elizabeth A Lund; Eric A Tanifum; Guoqiang Feng; Qaiser I Sheikh; Alvan C Hengge; Nicholas H Williams
Journal:  J Am Chem Soc       Date:  2008-09-18       Impact factor: 15.419

3.  Kinetic isotope effects for alkaline phosphatase reactions: implications for the role of active-site metal ions in catalysis.

Authors:  Jesse G Zalatan; Irina Catrina; Rebecca Mitchell; Piotr K Grzyska; Patrick J O'brien; Daniel Herschlag; Alvan C Hengge
Journal:  J Am Chem Soc       Date:  2007-07-14       Impact factor: 15.419

4.  Molecular cloning and characterization of the calcineurin subunit A from Plutella xylostella.

Authors:  Xi'en Chen; Yalin Zhang
Journal:  Int J Mol Sci       Date:  2013-10-15       Impact factor: 5.923

  4 in total

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