Abstract
Full-length human tyrosine hydroxylase 1 (hTH1) and a truncated enzyme lacking the 150 N-terminal amino acids were expressed in Escherichia coil and purified either with or without (6 x histidine) N-terminal tags. After reconstitution with 57Fe(II), the Mossbauer and X-ray absorption spectra of the enzymes were compared before and after dehydration by lyophilization. Before dehydration, >90% of the iron in hTH1 had Mossbauer parameters typical for highspin Fe(II) in a six-coordinate environment [isomer shift δ(1.8- 77K)=1.26-1.24mm s-1 and quadrupole splitting ΔE(Q)=2.68mm s-1]. After dehydration, the Mossbauer spectrum changed and 63% of the area could be attributed to five-coordinate high-spin Fe(II) (δ=1.07mm s-1 and ΔE(Q)=2.89 mm s-1 at 77K), whereas 28% of the iron remained as six- coordinate high-spin Fe(II) (δ=l.24 mm s-1 and ΔE(Q)=2.87 mm s-1 at 77 K). Similar changes upon dehydration were observed for truncated TH either with or without the histidine tag. After rehydration of hTH1 the spectroscopic changes were completely reversed. The X-ray absorption spectra of hTH1 in solution and in lyophilized form, and for the truncated protein in solution, corroborate the findings derived from the Mossbauer spectra. The pre-edge peak intensity of the protein in solution indicates six-coordination of the iron, while that of the dehydrated protein is typical for a five- coordinate iron center. Thus, the active-site iron can exist in different coordination states, which can be interconverted depending on the hydration state of the protein, indicating the presence or absence of a water molecule as a coordinating ligand to the iron. The present study explains the difference in iron coordination determined by X-ray crystallography, which has shown a five-coordinate iron center in rat TH, and by our recent spectroscopic study of human TH in solution, which showed a six-coordinated iron center.
| Originalsprache | Englisch |
|---|---|
| Zeitschrift | Journal of Biological Inorganic Chemistry |
| Jahrgang | 4 |
| Ausgabenummer | 2 |
| Seiten (von - bis) | 223-231 |
| Seitenumfang | 9 |
| ISSN | 0949-8257 |
| DOIs | |
| Publikationsstatus | Veröffentlicht - 01.04.1999 |
Fördermittel
the Research Council of Norway and the German Ministry for Education, Science, Research and Technology (BMBF). We are grateful for the technical assistance of Philip Antoniesen, Kathrin Uhlemann, and Sidsel E. Riise.