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Submit ReviewTransMoDE 3 Biotin is a biotinylated peptide capable of inducing both the degradation of target protein via lysosomal proteolysis and their bidirectional transcytosis of streptavidin across the blood-brain barrier. TransMoDE 3 Biotin is derived from the peptide Angiopep-2 (Cat. No. 8828).
M. Wt | 2611.88 |
Formula | C118H167N31O35S |
Sequence |
TFFYGGSRGKRNNFKTEEY (Modifications: Thr-1 = N-terminal Ac, Lys-10 = N(ε)-Ac-Lys, Lys-15 = N(ε)-Biotin-Lys |
Storage | Store at -20°C |
Purity | ≥95% (HPLC) |
InChI Key | SDTCWCCIHKRCLZ-MKHRACNQSA-N |
Smiles | O=C(N[C@@H]([C@H](O)C)C(N[C@@H](CC1=CC=CC=C1)C(N[C@@H](CC2=CC=CC=C2)C(N[C@@H](CC3=CC=C(C=C3)O)C(NCC(NCC(N[C@@H](CO)C(N[C@@H](CCCNC(N)=N)C(NCC(N[C@@H](CCCCNC(C)=O)C(N[C@@H](CCCNC(N)=N)C(N[C@@H](CC(N)=O)C(N[C@@H](CC(N)=O)C(N[C@@H](CC4=CC=CC=C4)C(N[C@@H](CCCCNC(CCCC[C@@H]5SC[C@@](N6)([H])[C@]5([H])NC6=O)=O)C(N[C@@H]([C@H](O)C)C(N[C@@H](CCC(O)=O)C(N[C@@H](CCC(O)=O)C(N[C@@H](CC7=CC=C(C=C7)O)C(O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)C |
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Solubility | Soluble to 1 mg/ml in water |
References are publications that support the biological activity of the product.
Howell et al (2024) Bifunctional Molecules That Induce Both Targeted Degradation and Transcytosis of Extracellular Proteins in Brain Cells. J Am Chem Soc 146 16404 PMID: 38855935
If you know of a relevant reference for TransMoDE 3 Biotin, please let us know.
Keywords: TransMoDE 3 Biotin, TransMoDE 3 Biotin supplier, TransMoDE, 3, Biotin, TransMoDE-3-Biotin, Biotinylated, angiopep-2, LRP1, transcytosis, lysosomal, degradation, BBB, brain, Endocytosis, LYTAC, Building, Blocks, 8829, Tocris Bioscience
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GPCRs can interact with multiple distinct transducers or regulatory proteins and these can be preferentially engaged in an agonist-specific manner giving rise to biased agonism. This poster discusses cutting edge GPCR signaling pharmacology and highlights therapeutic applications of biased agonism.