Cyclopentenone prostanoids (cyP) arise as important modulators of inflammation
and cellproliferation. Although their physiological significance has not been fully elucidated, their potent biologicaleffects have spurred their study as leads for the development of therapeutic agents. A key determinant ofcyP action is their ability to bind to thiol groups in proteins or in glutathione through Michael addition.Even though several protein targets for cyP addition have been identified, little is known about the structuraldeterminants from the protein or the cyP that drive this modification. The results herein presented providethe first evidence that cyP with different structures target distinct thiol sites in a protein molecule, namely,H-Ras. Whereas 15-deoxy-
12,14-prostagl
andin J
2 (15d-PGJ
2)
and
12-PGJ
2 preferentially target theC-terminal region containing cysteines 181
and 184, PGA
1 and 8-iso-PGA
1 bind mainly to cysteine 118,located in the GTP-binding motif. The biological counterparts of this specificity are the site-selectivemodification
and activation of H-Ras in cells
and the differential interaction of cyP with H, N,
and K-Rasproteins. Cysteine 184 is unique to H-Ras, whereas cysteine 118 is present in the three Ras homologues.Consistent with this, PGA
1 binds to
and activates H-, N-,
and K-Ras, thus differing from the preferentialinteraction of 15d-PGJ
2 with H-Ras. These results put forward the possibility of influencing the selectivityof cyP-protein addition by modifying cyP structure. Furthermore, they may open new avenues for thedevelopment of cyP-based drugs.