Ras GTPase

Error creating thumbnail:

An overview of Ras GTPase, its function, and significance in cellular processes

Ras GTPase is a family of proteins involved in transmitting signals within cells (cellular signal transduction). These proteins are a subfamily of the small GTPase superfamily and play a crucial role in the regulation of cell division, differentiation, and survival. Ras proteins are often referred to as molecular switches because they cycle between an active GTP-bound state and an inactive GDP-bound state.

Structure and Function

Ras proteins are small, approximately 21 kDa, and are composed of a single polypeptide chain. They have a highly conserved structure that includes a GTP-binding domain and a C-terminal hypervariable region that undergoes post-translational modifications, such as prenylation, which is essential for their membrane localization and function.

GTPase Activity

Ras proteins possess intrinsic GTPase activity, which allows them to hydrolyze GTP to GDP. This activity is crucial for their function as molecular switches. In their GTP-bound form, Ras proteins are active and can interact with various downstream effectors to propagate signaling pathways. The conversion to the GDP-bound form inactivates Ras, terminating the signal.

Regulation

Ras activity is tightly regulated by two main types of regulatory proteins:

• Guanine nucleotide exchange factors (GEFs): These proteins facilitate the exchange of GDP for GTP, activating Ras.
• GTPase-activating proteins (GAPs): These proteins enhance the intrinsic GTPase activity of Ras, promoting the hydrolysis of GTP to GDP and inactivating Ras.

Role in Signal Transduction

Ras proteins are key players in several signaling pathways, most notably the MAPK/ERK pathway. Upon activation by upstream signals, such as growth factors binding to receptor tyrosine kinases, Ras activates a cascade of kinases that ultimately lead to changes in gene expression and cellular responses.

Clinical Significance

Mutations in Ras genes, such as HRAS, KRAS, and NRAS, are implicated in various human cancers. These mutations often result in constitutively active Ras proteins that drive uncontrolled cell proliferation and survival, contributing to oncogenesis. KRAS mutations are particularly common in pancreatic cancer, colorectal cancer, and non-small cell lung cancer.

Research and Therapeutic Approaches

Given the role of Ras in cancer, it is a significant target for therapeutic intervention. However, directly targeting Ras has been challenging due to its high affinity for GTP/GDP and the lack of suitable binding pockets for small molecules. Recent advances include the development of inhibitors targeting specific mutant forms of Ras, such as KRAS G12C inhibitors.

Also see

• MAPK/ERK pathway
• GTPase
• Oncogene
• Signal transduction
• Cancer biology