Fluorescence quenching by nucleotides of the plasma membrane H -ATPase from Kluyveromyces lactis Article uri icon

abstract

  • The yeast plasma membrane H -ATPase isolation procedure was improved; a highly pure enzyme (90-95%25) was obtained after centrifugation on a trehalose concentration gradient. H -ATPase kinetics was slightly cooperative: Hill number = 1.5, S0.5 = 800 μM ATP, and turnover number = 36 s-1. In contrast to those of other P-type ATPases, H -ATPase fluorescence was highly sensitive to nucleotide binding; the fluorescence decreased 60%25 in the presence of both 5 mM ADP and AMP-PNP. Fluorescence titration with nucleotides allowed calculation of dissociation constants (Kd) from the binding site; Kd values for ATP and ADP were 700 and 800 μM, respectively. On the basis of amino acid sequence and homology model analysis, we propose that binding of the nucleotide to the N-domain is coupled to the movement of a loop β structure and to the exposure of the Trp505 residue located in the loop. The recombinant N-domain also displayed a large hyperbolic fluorescence quenching when ATP binds; however, it displayed a higher affinity for ATP (Kd = 100 μM). We propose for P-type ATPases that structural movements during nucleotide binding could be followed if a Trp residue is properly located in the N-domain. Further, we propose the use of trehalose in enzyme purification protocols to increase the purity and quality of the isolated protein and to perform structural studies. © 2007 American Chemical Society.
  • The yeast plasma membrane H%2b-ATPase isolation procedure was improved; a highly pure enzyme (90-95%25) was obtained after centrifugation on a trehalose concentration gradient. H%2b-ATPase kinetics was slightly cooperative: Hill number = 1.5, S0.5 = 800 μM ATP, and turnover number = 36 s-1. In contrast to those of other P-type ATPases, H %2b-ATPase fluorescence was highly sensitive to nucleotide binding; the fluorescence decreased 60%25 in the presence of both 5 mM ADP and AMP-PNP. Fluorescence titration with nucleotides allowed calculation of dissociation constants (Kd) from the binding site; Kd values for ATP and ADP were 700 and 800 μM, respectively. On the basis of amino acid sequence and homology model analysis, we propose that binding of the nucleotide to the N-domain is coupled to the movement of a loop β structure and to the exposure of the Trp505 residue located in the loop. The recombinant N-domain also displayed a large hyperbolic fluorescence quenching when ATP binds; however, it displayed a higher affinity for ATP (Kd = 100 μM). We propose for P-type ATPases that structural movements during nucleotide binding could be followed if a Trp residue is properly located in the N-domain. Further, we propose the use of trehalose in enzyme purification protocols to increase the purity and quality of the isolated protein and to perform structural studies. © 2007 American Chemical Society.

publication date

  • 2007-01-01