ASS1 (Argininosuccinate Synthase 1) is a urea cycle enzyme that catalyzes the synthesis of argininosuccinate from citrulline and aspartate. Recent studies highlight its antitumor role in triple-negative breast cancer (TNBC):
Mechanism: ASS1 binds to PHGDH (phosphoglycerate dehydrogenase), promoting its ubiquitination-mediated degradation. This suppresses serine synthesis, critical for cancer proliferation ( ).
Therapeutic Antibody Implications:
ASS1 loss correlates with poor prognosis in cancers.
Antibodies targeting ASS1-associated pathways (e.g., PHGDH inhibitors) are under investigation.
Asialoglycoprotein Receptor 1 (ASGR1) is a hepatic receptor studied for its role in SARS-CoV-2 entry:
Function: ASGR1 facilitates SARS-CoV-2 pseudovirus infection in hepatocytes independent of ACE2 ( ).
Antibody Applications:
Anti-ASGR1 antibodies block viral entry in vitro.
siRNA targeting ASGR1 reduces infection rates in hepatic cells.
While not specific to ASAT1, foundational antibody biology informs its potential applications:
Structure: Y-shaped glycoproteins with variable (antigen-binding) and constant (effector function) regions ( ).
Functional Mechanisms:
ASAT1 Clarification: The term "ASAT1" is not defined in current literature; potential typographical errors (e.g., ASS1, ASGR1) require verification.
Therapeutic Development: Antibodies targeting metabolic enzymes (e.g., ASS1) or viral entry receptors (e.g., ASGR1) represent emerging frontiers in oncology and virology.