RalA Activation Assay Biochem Kit (bead pull-down format) - 50 Assays

Product Uses Include:
Analysis of in vivo RalA activation

Introduction
The Ras family of small GTPases consists of at least 35 related human proteins that include the oncoproteins HRAS, KRAS and NRAS as the founding members (Colicelli 2004). The Ral proteins, RalA and RalB, share 58% identity to these oncoproteins and 85% identity with each other (Chardin and Tavitian 1986). Ral proteins play an important role in diverse cellular processes including endocytosis, exocytosis, oncogenesis and the regulation of transcription and cell morphology (Feig 2003)Like other small GTPases, Ral proteins become activated when they switch from the GDP-bound state to the GTP-bound state (Takai, Sasaki and Matozaki 2001), and it is the GTP-bound form that specifically interacts with their downstream effector proteins. The fact that Ral family effector proteins will specifically recognize the GTP-bound form of the protein has been exploited experimentally to develop a powerful affinity purification assay that monitors Ral protein activation (Hofer, Berdeaux and Martin 1998). The assay uses the Ral Binding Domain (RBD) of the effector protein RalBP1. The RBD protein motif has been shown to bind specifically to the GTP-bound form of Ral. The fact that the RBD region of RalBP1 has a high affinity for GTP-Ral makes it an ideal tool for affinity purification of GTP-Ral from cell lysates. The RalBP1-RBD protein supplied in this kit has been expressed as an His-tagged fusion protein in E. coli. and bound to colored beads. This allows one to “pulldown” GTP-Ral complexed with Ral-BP1-RBD beads. This assay provides a simple means of analyzing cellular RalA activities in a variety of systems. The amount of activated RalA is determined by a Western blot using a RalA specific antibody.

References
Chardin, P., and A. Tavitian. "The ral gene: a new ras-related gene isolated by the use of a synthetic probe." EMBO J 5 (1986): 2203-2208.
Colicelli, J. "Human RAS Superfamily Proteins and Related GTPases." Sci STKE 250, no. Re13 (2004): 1-53.
Feig, L.A. "Ral-GTPases: approaching their 15 minutes of fame." Trends in Cell Biology 13, no. 8 (2003): 419-425.
Hofer, F., R. Berdeaux, and G.S. Martin. "Ras-independent activation of Ral by a Ca2+-dependent pathway." Current Biology 8 (1998): 839-842.
Takai, Y., T. Sasaki, and T. Matozaki. "Small GTP-binding proteins." Physiol. Rev. 81 (2001): 153-208.

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