SPPL3 is an aspartyl protease that regulates glycosphingolipid (GSL) metabolism by controlling the enzyme B3GNT5. Its activity impacts HLA-I-mediated immune responses, as demonstrated in genome-wide screens.
Key Research Findings:
Mechanism of Action:
SPPL3 degrades B3GNT5, limiting the synthesis of neolacto-series GSLs (nsGSLs). Elevated nsGSLs in SPPL3-deficient cells sterically hinder HLA-I interactions with immune receptors like CD8+ T cells. SPPL3→B3GNT5 inhibition→nsGSLs↓→HLA-I accessibility↑
Functional Impact:
Reduced SPPL3 expression correlates with impaired T cell activation and tumor immune evasion.
In gliomas, dysregulated SPPL3-B3GNT5 pathways are linked to poorer patient survival.
Parameter
SPPL3-Dependent Effect
Citation
HLA-I accessibility
Enhanced antibody/receptor binding
CD8+ T cell response
Increased IFN-γ/GM-CSF production and cytotoxicity
SCP3/SYCP3 Antibody: Applications in Meiosis Research
SCP3 (SYCP3) is a structural protein critical for synaptonemal complex formation during meiosis. Antibodies against SCP3 are widely used in reproductive biology and cancer research.
Antibody Characteristics:
Host/Isotype: Mouse IgG1 (common across clones like 6F9C5 and 66409-1-Ig).
Applications:
Western Blot: Detects ~30 kDa band in human testis and cancer cell lines.
Immunohistochemistry (IHC): Localizes to spermatogonia and spermatocytes in testis.
Immunofluorescence (IF): Visualizes chromosome synapsis defects in oocytes.
Product Code
Reactivity
Applications
Key Validation Data
NB300-232
Human, Mouse
IHC, IF, WB
Strong nuclear staining in testis
ab181746 (6F9C5)
Human
WB, IHC (1:200 dilution)
Specificity confirmed via HEK293 transfection
66409-1-Ig
Human
WB, ELISA
Detected in DU 145 cells
Clinical Relevance:
Mutations in SYCP3 are associated with male infertility (azoospermia) and recurrent pregnancy loss.
SCP3 overexpression in cervical and kidney cancers suggests potential diagnostic utility.
Comparative Analysis of SPPL3 vs. SCP3 Antibodies
Feature
SPPL3 Antibody
SCP3 Antibody
Target Function
Immune regulation via GSL metabolism
Meiotic chromosome synapsis
Research Focus
Cancer immunology, infectious diseases
Reproductive biology, oncology
Therapeutic Potential
Immune checkpoint modulation
Diagnostic marker for infertility/cancer
Key Citations
Jongsma et al., 2020
Proteintech, Abcam
Future Directions
SPPL3: Explore nsGSL inhibition in combination therapies for glioma.
SCP3: Investigate its role in chemotherapy-induced meiotic defects.