In:
Protein Science, Wiley, Vol. 11, No. 3 ( 2002-03), p. 659-668
Kurzfassung:
The two amino acid residues, Asp 99 and Asp 201, involved in the coordination of the two calcium atoms in the X‐ray structure of bovine pancreatic (bp) DNase, were individually changed by site‐directed mutagenesis. The two altered proteins, brDNase(D99A) and brDNase(D201A) were expressed in Escherichia coli and purified by anion exchange chromatography. Equilibrium dialysis showed that mutation destroyed one Ca 2+ ‐binding site each in brDNase(D99A) and brDNase(D201A). Compared with bpDNase, the Vmax value for brDNase(D99A) remained unchanged and that for brDNase(D201A) was decreased, whereas the K m values for the two variants were increased two‐ to threefold when the DNA hydrolytic hyperchromicity assay was used. Like bpDNase, brDNase(D99A) was able to make double scission on duplex DNA with Mg 2+ plus Ca 2+ and was effectively protected by Ca 2+ from the trypsin inactivation. But under the same conditions, brDNase(D201A) lost the double‐scission ability and was not protected by Ca 2+ . Nevertheless, the two variant proteins retained the characteristics of the Ca 2+ ‐induced conformational changes and the Ca 2+ protection against the β‐mercaptoethanol disruption of the essential disulfide bond, suggesting that other weaker Ca 2+ ‐binding sites not found in the X‐ray structure were responsible for these properties. Therefore, the two structural calcium atoms are not for maintaining the overall conformation of the active DNase, as it has been indicated in the X‐ray analysis, but rather play the role in the fine‐tuning of the DNase activity.
Materialart:
Online-Ressource
ISSN:
0961-8368
,
1469-896X
Sprache:
Englisch
Verlag:
Wiley
Publikationsdatum:
2002
ZDB Id:
2000025-X
SSG:
12
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