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DOI 10.1016/j.bbrc.2010.11.009

Медицинская библиотека · Biochemical and biophysical research communications · 2010

Alkaline earth metals are not required for the restoration of the apoform of anthrax lethal factor to its holoenzyme state.

Säbel Crystal E, St-Denis Sylvie, Neureuther Joseph M, Carbone Ryan, Siemann Stefan

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Anthrax lethal factor (LF) is a zinc-dependent metalloendopeptidase previously shown to require calcium and magnesium for the restoration of its catalytic function upon exposure of the apoprotein (apoLF) to Zn(2+). Since concrete Ca(2+)/Mg(2+) binding sites have not been identified in LF, the effects of alkaline earth metals on the enzymatic function of holoLF (ZnLF) and on the reconstitution of apoLF were reinvestigated. The current study reveals alkaline earth metals to be inhibitory at concentrations higher than 1mM. A combination of activity/inhibition assays and Tb(3+) luminescence spectroscopy was employed to unequivocally establish the presence of at least one inhibitory low-affinity Ca(2+)-site in LF. A comparative analysis of apoLF preparations obtained by dialysis and centrifugal filtration (following treatment of ZnLF with chelators) revealed the exposure of apoLF to low equimolar amounts of Zn(2+) to be sufficient for the full restoration of the protein's catalytic competence, a finding constistent with the picomolar dissociation constant of ZnLF determined in this study. The previously documented requirement of Ca(2+) and Mg(2+) in apoLF reconstitution may be explicable on the basis of contamination of dialyzed apoprotein preparations with residual chelator, a phenomenon not encountered with apoLF obtained by centrifugal filtration.

Для цитирования: Säbel Crystal E, St-Denis Sylvie, Neureuther Joseph M, Carbone Ryan, Siemann Stefan. Alkaline earth metals are not required for the restoration of the apoform of anthrax lethal factor to its holoenzyme state.. Biochemical and biophysical research communications. 2010. DOI: 10.1016/j.bbrc.2010.11.009.

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