DSPE-PEG (2000) Biotin is an amphiphilic phospholipid–polyethylene glycol conjugate in which the DSPE hydrophobic anchor is connected to a PEG chain of intermediate length, terminating in a biotin moiety. Structurally, it combines a membrane-partitioning lipid domain with a hydrated PEG spacer that improves colloidal stability and reduces nonspecific interactions, while the terminal biotin provides a high-affinity handle for streptavidin/avidin binding. In PROTAC and targeted degradation workflows, such biotinylated PEG–lipids are valuable as modular linkers or surface-functionalization reagents to organize degrader components on protein scaffolds, immobilize or concentrate binding partners, and enable multivalent assembly that can enhance effective local concentration. The PEG spacer length supports flexible presentation of the biotin for robust capture, facilitating experimental designs such as streptavidin-mediated tethering, assay development, and membrane-associated studies of degradation-relevant interactions.
Structure of 385437-57-0
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DSPE-PEG (2000) Biotin is a lipid–polyethylene glycol conjugate designed to serve as a functional linker in targeted protein degradation workflows, enabling biotin-mediated handling and modular assembly of PROTAC-related components. Its amphiphilic DSPE anchor supports membrane or hydrophobic association, while the PEG spacer provides aqueous compatibility and reduced non-specific interactions. This product’s biotin functionality facilitates affinity-based capture and controlled positioning of targeting modules; detailed structural and reactivity considerations are provided below.
Structure: The molecule combines a phospholipid (DSPE) hydrophobic tail with a PEG ether chain and terminal biotin. It contains ester and ether linkages, a phosphodiester headgroup, and multiple heteroatoms that promote hydrogen bonding and water solubility. Overall, it is an amphiphilic conjugate with flexible PEG-mediated spacing.
Reactivity: For PROTAC construction, this linker is typically used in affinity-enabled assembly strategies rather than as a high-reactivity small-molecule coupling partner. Biotin can be exploited for strong streptavidin/avidin binding to organize components, while DSPE supports incorporation into lipid-containing systems. Assembly is commonly performed in buffered aqueous media under gentle mixing; covalent coupling, when required, is generally performed by reacting complementary functional groups on partner molecules using standard amide or thiol–maleimide chemistries with appropriate catalysts and bases.
* 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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