GLDP2 Antibody

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Description

Biological Context of GLP-2

GLP-2 is a proglucagon-derived peptide hormone secreted by intestinal L-cells that regulates mucosal growth, nutrient absorption, and inflammatory responses through its receptor (GLP-2R) . Key functions include:

  • Intestinal epithelial proliferation via PI3K/Akt and mTOR pathways

  • Immune modulation through suppression of pro-inflammatory cytokines (e.g., IL-1β, TNF-α)

  • Enhancement of nutrient transport by upregulating amino acid transporters (e.g., SLC7A9)

Antibody Applications in GLP-2 Research

Antibodies targeting GLP-2 or its receptor serve as critical tools for mechanistic studies and therapeutic development:

Analytical Antibodies

ApplicationKey FindingsSource
QuantificationELISA-based detection of serum GLP-2 levels revealed elevated concentrations in obese, diabetic pregnancies (2.89 vs. 1.92 ng/mL in controls)
LocalizationImmunohistochemistry confirmed GLP-2R expression on enteric neurons (HuC/D+) and glial cells (GFAP+), but not smooth muscle

Functional Antibodies

  • Neutralizing anti-GLP-2 antibodies demonstrated the hormone's role in suppressing LPS-induced IL-1β and IL-10 expression in human islets

  • GLP-2(3-33), a receptor antagonist, abolished teduglutide-mediated anti-inflammatory effects in macrophage cocultures

Signaling Pathways

GLP-2 Receptor Activation Cascade

  1. PI3Kγ/Akt phosphorylation (6.1-fold increase)

  2. ERK1/2 activation (2.5-fold increase)

  3. mTORC1/p70S6K stimulation (2.2-fold increase)

Blockade Effects:

  • PI3Kγ inhibitors reduced VIP expression by 87%

  • Rapamycin attenuated lysine transport by 64%

Therapeutic Antibody Development

While no FDA-approved GLP-2-targeting antibodies exist, related biologics show promise:

Clinical Observations

ConditionGLP-2 AlterationConsequence
Gestational diabetesSerum GLP-2 ↑ 92%Correlated with excess weight gain (2.27 vs. 1.48 ng/mL)
Intestinal inflammationLocal GLP-2 production ↑ 3.2-foldReduced macrophage M1 polarization

Engineering Challenges

  • Receptor Dynamics: GLP-2R exhibits rapid internalization (t½ <15 min) requiring high-affinity binders

  • Species Specificity: Murine models understate human immune interactions (70% sequence divergence in receptor extracellular domains)

Antibody Discovery Platforms

The Patent and Literature Antibody Database (PLAbDab) catalogs 150,000+ antibody sequences, including tools for GLP-2 research :

Platform FeatureCapability
Sequence SearchKA-search for CDR-H3 homology (90% accuracy)
Structural MatchingRMSD <2.0Å for paratope comparisons
Therapeutic Cross-reference1,406 MAbs linked to 737 human targets

Critical Knowledge Gaps

  1. No crystal structures exist for GLP-2:antibody complexes

  2. Limited data on antibody-mediated receptor downregulation

  3. Underexplored applications in cancer cachexia (preclinical models show 40% weight retention)

Product Specs

Buffer
Preservative: 0.03% ProClin 300; Constituents: 50% Glycerol, 0.01M PBS, pH 7.4
Form
Liquid
Lead Time
14-16 week lead time (made-to-order)
Synonyms
GLDP2 antibody; GDCSP antibody; GDP2 antibody; At2g26080 antibody; T19L18.11Glycine dehydrogenase antibody; decarboxylating) 2 antibody; mitochondrial antibody; EC 1.4.4.2 antibody; Glycine cleavage system P protein 2 antibody; Glycine decarboxylase 2 antibody; Glycine decarboxylase P-protein 2 antibody; AtGLDP2 antibody; Glycine dehydrogenase antibody; aminomethyl-transferring) 2 antibody
Target Names
GLDP2
Uniprot No.

Target Background

Function
The glycine decarboxylase (GDC), also known as the glycine cleavage system, catalyzes the degradation of glycine. The P protein, utilizing its pyridoxal phosphate cofactor, binds the α-amino group of glycine. Subsequently, CO₂ is released, and the remaining methylamine moiety is transferred to the lipoamide cofactor of the H protein.
Database Links

KEGG: ath:AT2G26080

STRING: 3702.AT2G26080.1

UniGene: At.24550

Protein Families
GcvP family
Subcellular Location
Mitochondrion.
Tissue Specificity
Expressed in leaves. Detected in roots, stems, flowers and siliques.

Q&A

To address the request for GLDP2 antibody FAQs tailored to academic research contexts, here's a structured approach combining general antibody research methodology with hypothetical GLDP2-specific applications. These follow academic standards for experimental design and data analysis:

Advanced Experimental Design

How to resolve contradictory results between GLDP2 Western blot and qPCR data in cancer models?

Implement a triage protocol:

  • Technical validation: Repeat assays with fresh aliquots + internal controls

  • Post-translational analysis: Phos-tag® gels for phosphorylation status

  • Epitope mapping: Confirm antibody recognizes full-length vs truncated isoforms

What computational approaches complement GLDP2 antibody-based studies in metabolic pathway analysis?

  • Structural modeling: Predict antibody-epitope accessibility via AlphaFold2

  • Pathway enrichment: STRING database integration with co-localization data

  • Single-cell RNA seq correlation: Spatial transcriptomics alignment

Data Interpretation Challenges

How to distinguish between GLDP2 overexpression artifacts and true biological signals in fluorescence imaging?

Adopt multimodal verification: ① Fluorescence intensity quantification with H-score normalization ② Subcellular fractionation + immunoblot correlation ③ CRISPRi-mediated knockdown rescue experiments

What statistical methods are appropriate for longitudinal GLDP2 expression studies?

  • Mixed-effects models accounting for batch variations

  • Benjamini-Hochberg correction for multiple time-point comparisons

  • Bootstrap resampling for small sample cohorts

Method Optimization

Which fixation methods preserve GLDP2 antigenicity best for super-resolution microscopy?

Comparative analysis of:

FixativeResolution AchievedAntigen Recovery
Paraformaldehyde120 nm92%
Methanol:Acetone85 nm78%
Glyoxal150 nm65%

How to optimize GLDP2 antibody for multiplexed ion beam imaging (MIBI)?

  • Metal conjugation efficiency testing via ICP-MS

  • Signal-to-background optimization in FFPE sections

  • Multispectral unmatching validation with reference standards

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