Ras: structural details to guide direct targeting

These proteins are mutated in about 20% of all human cancers and are thus important targets for drug discovery [1]. Major efforts over the last 20 years have not yielded drugs, promoting the notion that Ras is undruggable [2]. Recent advances in the structural biology of Ras provide new venues to be explored. The crystal structure of Ras has been known for over 25 years. Structural rearrangements that occur in the transition from Ras-GTP to Ras-GDP have been well studied, as GTP hydrolysis is at the center of how signaling through Ras is turned off. By the year 2000 we had the structures of several oncogenic mutants and the Ras/GAP complex revealing the transition state of the GAP-catalyzed reaction. Whether intrinsic or GAP-catalyzed, the hydrolysis reaction has traditionally been studied from the perspective of the active site without consideration of long-rage, global effects on catalysis. More recent focus has turned to the involvement of dynamics and conformational states of Ras-GTP with intrinsic hydrolysis on Ras. The study of allosteric modulation of the active site has revealed that in addition to known catalytic residues, switch II, helix 3, loop 7 and helix 4 may modulate hydrolysis, particularly in the complex with Raf [3]. These structural elements are affected by Ca2+ binding at an allosteric site remote from the nucleotide-binding pocket and thought to interact with the membrane [4]. Thus, within the context of allosteric modulation, hydrolysis of GTP on Ras is a global endeavor. However, given the existing framework of hydrolysis as being local to the active site, we have constructed an understanding of the effects of oncogenic mutants as a local phenomenon as well, focusing on the active site to study how it is perturbed in these mutants. In the context of global involvement of the Ras structure in catalysis, we must consider global effects due to oncogenic mutations. Indeed, our group has recently shown that the highly oncogenic Q61L mutant affects not only distal portions of Ras, but also of Raf-RBD in the complex [5]. Remarkably, the binding of Raf-RBD to wild type HRas promotes a decrease in flexibility of residues that coordinate Ca2+ at the remote allosteric site, adding to our proposed mechanism that interaction with the membrane primes the site for calcium binding Editorial to enhance intrinsic hydrolysis in the complex with Raf [3]. Thus, our current hypothesis is that Raf-RBD works synergistically with the membrane to …