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Identification of residues crucially involved in soluble guanylate cyclase activation
Author(s) -
Rothkegel Christiane,
Schmidt Peter M.,
Stoll Friederike,
Schröder Henning,
Schmidt Harald H.H.W.,
Stasch Johannes-Peter
Publication year - 2006
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/j.febslet.2006.06.079
Subject(s) - guanylate cyclase , chemistry , identification (biology) , biochemistry , gucy1a3 , gucy1b3 , guanylate cyclase 2c , biology , enzyme , ecology
The ubiquitous heterodimeric nitric oxide (NO) receptor soluble guanylate cyclase (sGC) plays a key role in various signal transduction pathways. Binding of NO takes place at the prosthetic heme moiety at the N‐terminus of the β 1 ‐subunit of sGC. The induced structural changes lead to an activation of the catalytic C‐terminal domain of the enzyme and to an increased conversion of GTP into the second messenger cyclic GMP (cGMP). In the present work we selected and substituted different residues of the sGC heme‐binding pocket based on a sGC homology model. The generated sGC variants were tested in a cGMP reporter cell for their effect on the enzyme activation by heme‐dependent (NO, BAY 41‐2272) stimulators and heme‐independent (BAY 58‐2667) activators. The use of these experimental tools allows the enzyme's heme content to be explored in a non‐invasive manner. Asp 44 , Asp 45 and Phe 74 of the β 1 ‐subunit were identified as being crucially important for functional enzyme activation. β 1 Asp 45 may serve as a switch between different conformational states of sGC and point to a possible mechanism of action of the heme dependent sGC stimulator BAY 41‐2272. Furthermore, our data shows that the activation profile of β 1 IIe 145 Tyr is unchanged compared to the native enzyme, suggesting that Tyr 145 does not confer the ability to distinguish between NO and O 2 . In summary, the present work further elucidated intramolecular mechanisms underlying the NO‐ and BAY 41‐2272‐mediated sGC activation and raises questions regarding the postulated role of Tyr 145 for ligand discrimination.