Pep1-AGL

Pep1-AGL is analog of Pep1-TGL (Cat. No. 1601), and a peptide containing the 'TGL' motif that corresponds to the C-terminus of the AMPA receptor GluA1 subunit.

Designed for biological research and industrial applications, not intended for individual clinical or medical purposes.

CAT No: R0833

Custom Peptide Synthesis
cGMP Peptide
  • Registration of APIs
  • CMC information required for an IND
  • IND and NDA support
  • Drug master files (DMF) filing
M.F/Formula
C40H69N11O14S
M.W/Mr.
960.11
Sequence
SSGMPLGAAGL
Labeling Target
AMPA receptor
Appearance
White lyophilised solid
Purity
>98 %

Pep1-AGL is a synthetic peptide compound recognized for its utility in biochemical and molecular biology research. Structurally, it belongs to the class of cell-penetrating peptides (CPPs), which are short amino acid sequences designed to facilitate the intracellular delivery of various molecular cargos. The sequence and physicochemical properties of Pep1-AGL allow it to interact with cellular membranes, making it an effective tool for studying membrane translocation mechanisms and intracellular trafficking. Its relevance extends to applications in protein delivery, peptide-functional studies, and the development of advanced research tools for probing cellular processes.

Cellular delivery research: Pep1-AGL is widely employed in investigations focused on the translocation of biomolecules across cellular membranes. By forming non-covalent complexes with proteins, nucleic acids, or other bioactive molecules, the peptide enables efficient intracellular delivery without compromising the integrity of the cargo. Researchers utilize it to study the kinetics, efficiency, and specificity of cellular uptake mechanisms, providing valuable insights into endocytosis-independent transport pathways and the fundamental principles governing cell-penetrating peptide function.

Protein transduction studies: In functional proteomics and cell signaling research, Pep1-AGL serves as a carrier for the intracellular delivery of recombinant proteins, enzymes, or functional peptides. Its ability to transport biologically active macromolecules into the cytoplasm or subcellular compartments allows scientists to investigate protein function in live cells, modulate signaling cascades, and dissect protein-protein interactions in their native cellular context. This application is particularly significant in elucidating the role of specific proteins in complex cellular networks.

Peptide engineering and structure-activity analysis: The modular nature of Pep1-AGL makes it an ideal template for peptide engineering studies. Researchers often modify its sequence to explore the relationship between amino acid composition, structural conformation, and membrane-penetrating efficiency. Such investigations contribute to the rational design of next-generation CPPs with enhanced specificity, reduced cytotoxicity, or tailored delivery profiles, advancing the broader field of peptide-based delivery systems.

Biochemical assay development: The unique properties of Pep1-AGL support its use in the development and optimization of cell-based assays. By facilitating the direct introduction of molecular probes, reporters, or inhibitors into living cells, the peptide enables precise monitoring of intracellular events, enzyme activities, or signal transduction pathways. This functionality is instrumental in high-throughput screening platforms, where reliable and reproducible delivery of assay components is critical to data quality and interpretability.

Intracellular imaging and molecular tracking: Labeling Pep1-AGL with fluorescent tags or other detectable markers allows researchers to visualize peptide uptake, intracellular localization, and trafficking dynamics in real time. Such studies inform the spatial and temporal aspects of membrane translocation and cargo release, supporting the development of advanced imaging protocols and the validation of delivery strategies. This approach contributes to a deeper understanding of cellular dynamics and the optimization of peptide-mediated delivery for research applications.

Solubility
-20 °C
InChI
InChI=1S/C40H69N11O14S/c1-20(2)13-26(36(60)43-15-30(54)45-23(6)34(58)46-22(5)33(57)42-16-32(56)48-27(40(64)65)14-21(3)4)49-38(62)29-9-8-11-51(29)39(63)25(10-12-66-7)47-31(55)17-44-37(61)28(19-53)50-35(59)24(41)18-52/h20-29,52-53H,8-19,41H2,1-7H3,(H,42,57)(H,43,60)(H,44,61)(H,45,54)(H,46,58)(H,47,55)(H,48,56)(H,49,62)(H,50,59)(H,64,65)/t22-,23-,24-,25-,26-,27-,28-,29-/m0/s1
InChI Key
DKRJFJKDHRZRQJ-PJYAFMLMSA-N
Isomeric SMILES
C[C@@H](C(=O)N[C@@H](C)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)O)NC(=O)CNC(=O)[C@H](CC(C)C)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCSC)NC(=O)CNC(=O)[C@H](CO)NC(=O)[C@H](CO)N

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