S100 Calcium Binding Protein A4, Recombinant, Human (S100A4)

S100A4 (also metastasin, Mtsl and calvasculin) is an 11 kD member of the S100 (soluble in 100% saturated ammonium sulfate) family of proteins (1-5). The S100 family is a further classified as a member of the EF-hand superfamily of Ca++ -binding proteins. These participate in both calcium-dependent and calcium-independent protein-protein interactions. The hallmark of this superfamily is the EF-hand motif that consists of a Ca++ -binding site flanked by two a-helices (helix E and helix F) that were originally identified in a right-handed model of carp muscle calcium-binding protein (6). Human S100A4 is 101 amino acids (aa) in length (1, 2). It contains two EF hand domains, one between aa # 12-47, and a second between aa # 50-85. The first domain has a 14 aa cation-binding motif and binds Ca++ with low affinity. The second Ca++ -binding motif is 12 aa in length and binds Ca++ with high affinity. S100A4 has no classical signal sequence but is secreted from cells (3, 7). Human S100A4 shares 93% and 95% aa identity with mouse and dog S100A4, respectively. S100A4 reportedly exists as dimer (8, 9, 10). Extracellular S100A4 is reported to induce MMP production, activate MMPs, promote neurite outgrowth and stimulate cardiomyocyte proliferation (4, 10, 11, 12, 13). Within the cell, dimers are likely the functional unit. Here, they are constitutive homo- or heterodimers (with S100A1) that interact with Ca++, undergo a conformational change, and subsequently bind to cytoplasmic targets. Known targets include p53, myosin heavy chain II, F-actin and liprin b1 (4, 14). In general, it can be said that S100A4 blocks target phosphorylation and multimerization (4, 7, 14). S100A4 activity has been associated with cell transformation. It seems likely this is either coincidental, or a consequence, rather than a cause of transformation (3).\n\nActivity: \nMeasured by its ability to induce neurite outgrowth from E13 chick dorsal root ganglia neurons. Immobilized rhS100A4 (at a 3uL droplet containing 90ng) on nitrocellulose-coated microplate is sufficient to significantly enhance neurite outgrowth.\n\nStorage and Stability:\nLyophilized powder may be stored at -20 degrees C. Reconstitute with sterile PBS and carrier protein (0.1% HSA or BSA). Aliquot and store at -20 degrees C. Reconstituted product is stable for 6 months at -20 degrees C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.

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SPECIFICATIONS

Catalog Number

S0051-83E

Size

50ug

Form

Supplied as a lyophilized powder from PBS, 1mM DTT. Reconstitute with PBS, carrier protein to (same/more than)0.1mg/ml.

Purity

(same/more than) 95%, as determined by SDS-PAGE and visualized by silver stain. Endotoxin: (same/less than)1.0 EU/1ug

References

1. Engelkamp, D. et al. (1992) Biochemistry 31:10258. 2. Tomida, Y. et al. (1992) Biochem. Biophys. Res. Commun. 189:1310. 3. Garrett, S.C. et al. (2006) J. Biol. Chem. 281:677. 4. Santamaria-Kisiel, L. et al. (2006) Biochem. J. 396:201. 5. Donato, R. (2001) Int. J. Biochem. Mol. Biol. 33:637. 6. Kretsinger, R.H. & C.E. Nockolds (1973) J. Biol. Chem. 248:3313. 7. Helfman, D.M. et al. (2005) Br. J. Cancer 92:1955. 8. Burkitt, W.I. et al. (2003) Biochem. Soc. Trans. 31:985. 9. Vallaly, K.M. et al. (2002) Biochemistry 41:12670. 10. Novitskaya, V. et al. (2000) J. Biol. Chem. 275:41278. 11. Stary, M. et al. (2006) Biochem. Biophys. Res. Commun. 343:555. 12. Semov, A. et al. (2005) J. Biol. Chem. 280:20833. 13. Saleem, M. et al. (2006) Proc. Natl. Acad. Sci. USA 103:14825. 14. Kriajevska, M. et al. (2002) J. Biol. Chem. 277:5229.