PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
June 1, 1985Journal of Biological Chemistry59 citationsOpen Access

Two distinct classes of nucleotide binding sites in sarcoplasmic reticulum Ca-ATPase revealed by 2‘,3‘-O-(2,4,6-trinitrocyclohexadienylidene)-ATP.

View Full Paper
YDYves DupontRPRichard PougeoisMRMichel Ronjat

Key Result

The Ca-ATPase enzyme possesses two classes of ATP binding sites whose affinity and interaction are modulated by H+ and Mg2+ concentrations.

Structured PICO

P
Population
Sarcoplasmic reticulum Ca-ATPase enzyme
I
Intervention
2',3'-O-(2,4,6-trinitrocyclohexadienylidene) (TNP)-nucleotides
C
Comparator
ATP
O
Outcome
Nucleotide binding site characteristics (affinity, concentration, and response to H+ and Mg2+ concentrations)surrogate

The sarcoplasmic reticulum Ca-ATPase possesses two distinct classes of ATP binding sites whose affinity and interaction are modulated by H+ and Mg2+ concentrations.

Abstract

It was previously reported that 2',3'-O-(2,4,6-trinitrocyclohexadienylidene) (TNP)-nucleotides bind with high affinity to the sarcoplasmic reticulum Ca-ATPase (Dupont, Y., Chapron, Y., and Pougeois, R. (1982) Biochem. Biophys. Res. Commun. 106, 1272-1279 and Watanabe, T., and Inesi, G. (1982) J. Biol. Chem. 257, 11510-11516). Here we report a study of the Ca-ATPase nucleotide binding sites using TNP-nucleotides. Competition at equilibrium between TNP-nucleotides and ATP was measured in the absence of calcium; it was found that TNP-nucleotides and ATP competitively bind to two classes of sites of equal concentration (3.5 nmol/mg). The ATP dissociation constants for the two classes of sites were found to be sensitive to H+ and Mg2+ concentrations. In the absence of Mg2+ (independently of pH) or at acid pH (independently of Mg2+ concentration), the nucleotide sites behave like one single family of sites of intermediate affinity (Kd = 20 microM). They split into two classes of sites of high (Kd = 2-4 microM) and low (Kd greater than 1 mM) affinity at pH values higher than neutral and in the presence of Mg2+. The calcium-activated ATP hydrolysis is accelerated by TNP-ATP (or TNP-AMP-PNP) binding on the phosphorylated enzyme. It is concluded 1) that the Ca-ATPase enzyme possesses two classes of ATP binding sites, 2) that the affinity of these two sites and the nature of their interaction is modulated by the H+ and Mg2+ concentrations, and 3) that the hydrolytic activity of the high affinity ATP binding site is activated by ATP or TNP-AMP-PNP (or TNP-ATP) binding in a low affinity ATP binding site.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Dupont et al. (1985) studied this question. TNP-nucleotides vs. ATP was evaluated on ATP dissociation constants and binding site classes. The Ca-ATPase enzyme possesses two classes of ATP binding sites whose affinity and interaction are modulated by H+ and Mg2+ concentrations.

synapsesocial.com/papers/6a63a0c84f5ef41b946ae545https://doi.org/10.1016/s0021-9258(17)39599-6
Ask AI
Helpful
Bookmark
Share
View Full Paper