Biotin-PEG3-Azide is a heterobifunctional linker reagent combining a biotin affinity handle with a short, flexible poly(ethylene glycol) spacer terminated by an azide group. Structurally, it provides a biotin moiety for strong binding to streptavidin or avidin, while the PEG3 chain improves solubility and reduces nonspecific interactions by adding conformational flexibility between conjugated partners. The azide functionality enables efficient bioorthogonal labeling via azide–alkyne cycloaddition (CuAAC or strain-promoted variants), allowing researchers to attach the biotin-bearing linker to PROTAC-related components or other targeting ligands bearing complementary alkyne groups. In targeted protein degradation workflows, this reagent is particularly valuable for constructing degraders or assay probes that require site-specific conjugation and subsequent capture or enrichment through biotin–avidin interactions. It supports robust experimental design for monitoring conjugate formation, optimizing linker placement, and facilitating downstream detection or pull-down assays.
Structure of 875770-34-6
* For research and manufacturing use only. Not for human or clinical use.
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Biotin-PEG3-Azide is a polyethylene glycol-based linker bearing a terminal azide functionality and a biotin handle, enabling modular assembly of targeted protein degradation (PROTAC) constructs and related affinity reagents. Its PEG segment improves aqueous solubility and provides conformational flexibility, while the azide group serves as a versatile reaction handle for bioorthogonal conjugation. The biotin moiety can facilitate downstream capture and analytical workflows. Detailed structural and reactivity considerations are provided below.
Structure: Biotin-PEG3-Azide features a biotin scaffold connected through a short PEG chain to a terminal azide group. The linker contains ether linkages within the PEG segment and an azide substituent suitable for click-type chemistry. Overall, it is designed for hydrophilic behavior and flexible presentation of the reactive handle.
Reactivity: The azide enables copper-catalyzed azide–alkyne cycloaddition or related azide-based conjugation strategies commonly used to connect PROTAC components under mild, aqueous-compatible conditions. Reaction design typically follows established click-chemistry principles, where the azide reacts with an appropriate alkyne partner to form a stable triazole linkage. Solvent systems are selected to maintain solubility and preserve protein-binding ligands; catalysts and ligand-free or ligand-assisted copper systems are chosen based on compatibility with sensitive functional groups.
* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2
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