Biophysical characterization of S100A8 and S100A9 in the absence and presence of bivalent cations.

Article Details

Citation

Vogl T, Leukert N, Barczyk K, Strupat K, Roth J

Biophysical characterization of S100A8 and S100A9 in the absence and presence of bivalent cations.

Biochim Biophys Acta. 2006 Nov;1763(11):1298-306. Epub 2006 Aug 25.

PubMed ID
17050004 [ View in PubMed
]
Abstract

S100A8 and S100A9 are two proinflammatory molecules belonging to the S100 family of calcium-binding proteins. Common to all S100 proteins S100A8 and S100A9 form non-covalently associated complexes which have been shown to exhibit different functional properties. Besides dimerization, recent research is focused on the importance of higher oligomeric structures of S100 proteins induced by bivalent cations. While S100A8/S100A9-heterodimers are formed in the absence of calcium, tetramerization is strictly calcium-dependent. Heterodimer formation is not a simple process and our biophysical analyses (FRET, ESI-MS) demonstrate that simply mixing both subunits is not sufficient to induce complex formation. Steps of denaturation/renaturation are necessary for the recombinant complex to show identical biophysical properties as S100A8/S100A9 obtained from granulocytes. In addition to calcium both proteins are able to bind zinc with high affinity. Here we demonstrate for the first time by different biophysical methods (MALDI-MS, ESI-MS, fluorescence spectroscopy) that zinc-binding, like calcium, induces (S100A8/S100A9)(2)-tetramers. Using mass spectrometric investigations we demonstrate that zinc triggers the formation of (S100A8/S100A9)(2)-tetramers by zinc-specific binding sites rather than by interactions with calcium-specific EF-hands. The zinc-induced tetramer is structurally very similar to the calcium-induced tetramer. Thus, like calcium, zinc acts as a regulatory factor in S100A8/S100A9-dependent signaling pathways.

DrugBank Data that Cites this Article

Drug Targets
DrugTargetKindOrganismPharmacological ActionActions
CalciumProtein S100-A8ProteinHumans
Unknown
Not AvailableDetails
CalciumProtein S100-A9ProteinHumans
Unknown
Not AvailableDetails
ZincProtein S100-A8ProteinHumans
Unknown
Not AvailableDetails
ZincProtein S100-A9ProteinHumans
Unknown
Not AvailableDetails
Zinc acetateProtein S100-A8ProteinHumans
Unknown
Not AvailableDetails
Zinc acetateProtein S100-A9ProteinHumans
Unknown
Not AvailableDetails
Zinc chlorideProtein S100-A8ProteinHumans
Unknown
Regulator
Details
Zinc chlorideProtein S100-A9ProteinHumans
Unknown
Regulator
Details
Zinc sulfate, unspecified formProtein S100-A8ProteinHumans
Unknown
Regulator
Details
Zinc sulfate, unspecified formProtein S100-A9ProteinHumans
Unknown
Regulator
Details