N-Peptide (trifluoroacetate salt)

N-Peptide (Trifluoroacetate Salt) is a short regulatory motif stabilized by TFA counterions for improved solubility. Residue selection enables hydrogen bonding and adaptable secondary structure. Researchers investigate its binding to structured domains and polymer interfaces. Applications include signaling-motif mapping, biophysical analysis, and peptide-material studies.

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

CAT No: R2816

Synonyms/Alias:H-Trp-Glu-Tyr-Ile-Pro-Asn-Val-OH.TFA

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M.F/Formula
C47H62F3N9O14
M.W/Mr.
1034
Sequence
One Letter Code:WEYIPNV
Three Letter Code:H-Trp-Glu-Tyr-Ile-Pro-Asn-Val-OH.TFA

N-Peptide (trifluoroacetate salt) is a synthetic peptide compound widely utilized in biochemical and molecular biology research. As a peptide sequence presented in the trifluoroacetate salt form, it offers enhanced solubility and stability, making it suitable for a variety of experimental contexts. Its defined amino acid composition and robust physicochemical properties support its use in peptide-based investigations, including structure-activity studies, functional assays, and as a tool for probing protein interactions. The availability of N-Peptide in a purified, research-grade format enables precise manipulation in laboratory protocols, facilitating reproducible results and meaningful scientific insights.

Peptide structure-function analysis: N-Peptide is frequently employed in studies aiming to elucidate the relationship between peptide sequence and biological activity. Researchers utilize it as a model substrate to investigate how specific amino acid arrangements influence folding, binding affinities, or receptor interactions. Such applications are fundamental for advancing the understanding of peptide-mediated signaling pathways, molecular recognition events, and the development of structure-based design strategies in peptide science.

Protein-protein interaction mapping: The peptide serves as a valuable probe in the identification and characterization of protein-protein interactions. By incorporating N-Peptide into binding assays, pull-down experiments, or surface plasmon resonance platforms, scientists can dissect the molecular determinants governing complex formation. These insights are critical for unraveling the mechanisms underlying cellular communication, regulatory networks, and the assembly of multiprotein complexes.

Peptide synthesis validation: In synthetic chemistry and peptide engineering, N-Peptide is utilized as a reference standard or benchmarking tool to assess the efficiency and fidelity of solid-phase peptide synthesis protocols. Its well-characterized sequence allows for the calibration of purification systems, optimization of cleavage conditions, and verification of analytical methods such as mass spectrometry or high-performance liquid chromatography. This application supports the advancement of peptide manufacturing technologies and quality control processes.

Immunological assay development: The defined sequence and purity of N-Peptide make it an excellent candidate for use as an antigen or epitope in immunoassay development. It can be employed to generate peptide-specific antibodies, calibrate enzyme-linked immunosorbent assays (ELISAs), or serve as a control in immunodetection workflows. These applications are instrumental in supporting the development of sensitive and specific detection systems for research in immunology, diagnostics, and biomarker discovery.

Cell signaling pathway studies: As a bioactive peptide, N-Peptide can be introduced into cellular systems to probe signaling cascades, receptor activation, or downstream effector responses. Its application in cell-based assays enables researchers to dissect the functional consequences of peptide-receptor engagement, evaluate potential modulators, and explore the dynamics of intracellular signaling networks. This approach provides valuable mechanistic insights and supports the identification of novel targets for further biochemical investigation.

InChI
InChI=1S/C45H61N9O12.C2HF3O2/c1-5-24(4)38(44(64)54-18-8-11-34(54)43(63)51-33(21-35(47)56)42(62)52-37(23(2)3)45(65)66)53-41(61)32(19-25-12-14-27(55)15-13-25)50-40(60)31(16-17-36(57)58)49-39(59)29(46)20-26-22-48-30-10-7-6-9-28(26)30;3-2(4,5)1(6)7/h6-7,9-10,12-15,22-24,29,31-34,37-38,48,55H,5,8,11,16-21,46H2,1-4H3,(H2,47,56)(H,49,59)(H,50,60)(H,51,63)(H,52,62)(H,53,61)(H,57,58)(H,65,66);(H,6,7)/t24-,29-,31-,32-,33-,34-,37-,38-;/m0./s1
InChI Key
ARSBFYVPTHWQLV-ZVBBAADPSA-N

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