Peptide · Research Monograph · DPP-IV-resistant 33-amino-acid GLP-2 receptor agonist peptide ([Gly2]GLP-2 / teduglutide-type analog)

GLP-2 TZ

Intestinal Adaptation Studies

GLP-2 TZ is a 33 amino acid analog of glucagon-like peptide-2, the teduglutide-type sequence. A substitution at the second position resists DPP-4, the enzyme that clears the natural hormone within minutes. Studies have measured intestinal villus height, crypt depth, and mucosal barrier function in resection and injury models.

For laboratory research use only - not for human or animal use

Available in the Eon catalog - GLP-2 TZ from $85.00 Certificate of analysis (PDF)

Molecular data

Molecular formulaAvailable on request
Molecular weight3752 Da
SequenceHADGSFSDEMNTILDNLAARDFINWLIQTKITD
Sequence length33 residues
Physical formLyophilized powder (5mg)
Available sizes10mg, 30mg, 60mg, 100mg

How it works

GLP-2R Agonism

Glucagon-Like Peptide-2 Receptor Activation

GLP-2-TZ is a synthetic analog of glucagon-like peptide-2 (GLP-2), a 33-amino acid hormone secreted by enteroendocrine L-cells in the distal intestine. It binds and activates the GLP-2 receptor (GLP-2R), a G-protein coupled receptor expressed primarily on intestinal subepithelial myofibroblasts, enteric neurons, and intestinal epithelial cells. GLP-2R activation initiates trophic signaling cascades relevant to intestinal adaptation research.

  • Selective GLP-2R agonist (Gs-coupled GPCR)
  • Activates cAMP/PKA signaling in intestinal subepithelial cells
  • Downstream IGF-1 and EGF receptor cross-talk measured
Mucosal Trophism

Intestinal Villus Growth & Crypt Expansion

GLP-2 signalling is studied against intestinal mucosal growth, with crypt cell proliferation and apoptosis in villus epithelial cells as the measured endpoints. In short bowel syndrome research models, villus height, crypt depth and total mucosal surface area were recorded — the parameter that determines absorptive capacity.

  • Intestinal villus height and crypt depth measured
  • Enterocyte apoptosis measured in mucosal injury models
  • Intestinal mucosal surface area measured
DPP-IV Resistance

Extended Biological Half-Life

Native GLP-2 is rapidly degraded by dipeptidyl peptidase-IV (DPP-IV) cleaving at position 2, limiting its half-life to ~7 minutes. GLP-2-TZ incorporates structural modifications (analogous to teduglutide's Gly2→Ala2 substitution) that confer resistance to DPP-IV cleavage, extending the plasma half-life and enabling more sustained GLP-2R activation in preclinical and clinical contexts.

  • Resistant to DPP-IV cleavage at N-terminus
  • Extended plasma half-life vs. native GLP-2
  • More sustained GLP-2R activation in research models

What the research shows

GI Research

Short Bowel Models

GLP-2 analogs structurally related to GLP-2-TZ are a primary research model for intestinal adaptation. Teduglutide is an approved pharmaceutical in this class; this research material is not.

Mucosal Biology

Intestinal Adaptation

GLP-2R activation is studied against intestinal adaptation endpoints including villus hyperplasia, nutrient transporter expression and mucosal blood flow — measured in resection and injury models.

Barrier Function

Intestinal Permeability

GLP-2 signalling has been studied in intestinal barrier function research, with paracellular permeability and tight junction integrity measured in injury models — endpoints also used in inflammatory bowel disease research.

IBD Research

Crohn's Disease Models

In rodent models of colitis and Crohn's disease, mucosal inflammation, barrier integrity and mucosal repair endpoints were measured following GLP-2 analog administration.

Specification

Also Known AsGLP-2 Analog, [Gly2]GLP-2, Teduglutide-type GLP-2
TypeSynthetic GLP-2 receptor agonist peptide
Length33 amino acids
Molecular Weight~3752 Da
Target ReceptorGLP-2 Receptor (GLP-2R, GPCR)
MechanismDPP-IV-resistant GLP-2R agonist; intestinal trophic signaling
FormLyophilized powder (5mg)
Purity≥99% (HPLC verified)
TestingThird-party HPLC, Mass Spec, Endotoxin
Storage-20°C for long-term stability
SolubilityBacteriostatic water; sterile saline
COAIncluded with every order
Molecular FormulaAvailable on request
AppearanceWhite to off-white powder
Quantity5mg
Stability24 months from manufacture date when stored properly

Frequently asked questions

What is GLP-2-TZ and how does it relate to teduglutide?

GLP-2-TZ is a synthetic analog of glucagon-like peptide-2 (GLP-2), designed with structural modifications that confer resistance to DPP-IV degradation — analogous to the modifications found in teduglutide (Gattex/Revestive), the FDA-approved GLP-2 analog for short bowel syndrome. Native GLP-2 has a ~7-minute plasma half-life due to rapid DPP-IV cleavage at position 2; teduglutide and related analogs like GLP-2-TZ incorporate an Ala2 substitution (replacing Gly2 in native GLP-2) to resist this degradation. GLP-2-TZ is used as a research tool to study GLP-2R-mediated intestinal physiology.

What is the GLP-2 receptor and where is it expressed?

The GLP-2 receptor (GLP-2R) is a G-protein coupled receptor (GPCR) whose expression is highly restricted to the gastrointestinal tract. Primary expression sites include intestinal subepithelial myofibroblasts (ISEMFs), enteric neurons of the submucosal and myenteric plexus, and scattered enteroendocrine cells. This tissue specificity distinguishes GLP-2R from GLP-1R, which is expressed broadly (pancreas, heart, brain, kidney). The restricted expression pattern means GLP-2 analogs primarily affect intestinal physiology, which is central to their research relevance for intestinal adaptation and short bowel syndrome.

What is short bowel syndrome (SBS) and why is GLP-2 relevant?

Short bowel syndrome (SBS) results from surgical resection of large portions of the small intestine, leaving insufficient absorptive surface area to maintain nutrition without parenteral support. The intestine undergoes adaptation after resection — villus hyperplasia and crypt expansion — which GLP-2 signalling modulates. GLP-2 rises after intestinal resection, indicating a physiological role in that adaptation. Teduglutide, the approved GLP-2 analog, acts on this mechanism; that approval covers the licensed medicine only, not this research material.

What research models is GLP-2-TZ used in?

GLP-2-TZ is used in intestinal biology research models including: small bowel resection/intestinal adaptation models (rodents); intestinal organoid/enteroid culture systems for mucosal growth studies; intestinal permeability and barrier function assays; inflammatory bowel disease models (colitis, Crohn's); and in vitro GLP-2R binding and signaling studies. The compound is also used to investigate paracrine signaling between enteric neurons, ISEMFs, and epithelial cells in the intestinal niche.

Is there an FDA-approved GLP-2 drug, and how does GLP-2-TZ differ?

Yes — teduglutide (Gattex in the US, Revestive in Europe) is an FDA-approved GLP-2 analog for SBS with intestinal failure in adults, approved in 2012. GLP-2-TZ is not the same compound as teduglutide and has not undergone independent clinical development. GLP-2-TZ is sold as a research tool compound to study GLP-2 receptor biology and is not for human therapeutic use. Researchers use it to study the mechanistic underpinnings of GLP-2 receptor pharmacology without the cost and regulatory restrictions of the pharmaceutical product.

How should GLP-2-TZ be stored?

Store lyophilized GLP-2-TZ at -20°C, protected from light, and minimize freeze-thaw cycles by preparing single-use aliquots. For cell culture experiments, ensure laboratory solutions are sterile-filtered.

For laboratory research use only. Not a drug, supplement, or medical product; not for human or animal use. All findings referenced are from published preclinical/laboratory research.