CBLB - E3 ubiquitin-protein ligase | Elisa - Clia - Antibody - Protein

Background

CBL (Casitas B-lineage Lymphoma) proteins are a family of E3 ubiquitin ligases that play a crucial role in the regulation of cell signaling pathways. These proteins are essential for targeting specific substrates for ubiquitination, a process that marks proteins for degradation by the proteasome, alters their cellular location, affects their activity, or promotes/prevents protein interactions. The CBL family includes CBL, CBL-b, and CBL-c (also known as CBL-3), all of which share a common structural framework and functional properties. CBL proteins are involved in a variety of cellular processes, including signal transduction, cell growth, and differentiation, by regulating receptor tyrosine kinases (RTKs) and other signaling proteins. Their function is critical for maintaining cellular homeostasis and preventing aberrant signaling that can lead to diseases such as cancer.

Protein Structure

CBL proteins have a complex domain architecture that enables their function as E3 ubiquitin ligases:

• N-terminal Tyrosine Kinase Binding (TKB) domain: This domain consists of a four-helix bundle (4H), a calcium-binding EF-hand, and a variant SH2 domain, which collectively allow CBL to bind phosphorylated tyrosine residues on target proteins.
• RING Finger domain: This domain mediates the transfer of ubiquitin from an E2 ubiquitin-conjugating enzyme to the substrate, a key step in the ubiquitination process.
• Proline-rich region: This area interacts with SH3 domain-containing proteins, facilitating the assembly of signaling complexes.
• C-terminal Ubiquitin-Associated (UBA) domain: This domain binds to ubiquitin chains, which may help in substrate recognition and processivity of ubiquitination.

Classification and Subtypes

CBL proteins are classified based on their structural and functional characteristics:

• CBL (also known as c-CBL): The prototype member of the family, involved in ubiquitination and degradation of activated RTKs.
• CBL-b: Similar to c-CBL but with distinct expression patterns and some functional differences, particularly in immune cells.
• CBL-c (CBL-3): A less well-studied member with roles similar to c-CBL and CBL-b but with unique tissue distribution and possibly distinct substrates.

Function and Biological Significance

CBL proteins perform several critical functions:

• Regulation of RTKs: CBL proteins ubiquitinate activated RTKs, leading to their internalization and degradation, thus terminating signal transduction pathways that promote cell proliferation and survival.
• Signal Transduction: By ubiquitinating various signaling proteins, CBL proteins modulate pathways such as the Ras/MAPK and PI3K/Akt pathways, which are important for cell growth, differentiation, and survival.
• Immune Response: CBL-b is particularly important in immune cells, where it regulates the activation of T-cells and other immune responses, maintaining immune homeostasis and preventing autoimmunity.

Clinical Issues

Alterations in CBL function are linked to various diseases:

• Cancer: Mutations in the CBL gene can lead to its loss of function or gain of aberrant functions, contributing to uncontrolled cell growth and resistance to apoptosis, commonly seen in hematological malignancies like leukemia and some solid tumors.
• Immune Disorders: Dysregulation of CBL-b can lead to immune system dysfunctions, including autoimmune diseases and impaired immune responses.
• Developmental Disorders: Abnormal CBL activity can affect developmental signaling pathways, leading to developmental anomalies.

Summary

CBL proteins are vital E3 ubiquitin ligases involved in the regulation of key signaling pathways by targeting specific proteins for ubiquitination. They consist of multiple domains that facilitate substrate recognition and ubiquitin transfer, playing crucial roles in signal transduction, cell growth, and immune regulation. Dysregulation of CBL proteins is associated with various diseases, particularly cancers and immune disorders, underscoring their importance in maintaining cellular homeostasis. Understanding the precise mechanisms by which CBL proteins function and their role in disease pathogenesis continues to be a critical area of biomedical research, offering potential avenues for therapeutic intervention.