Abstract
Aqueous Diels–Alder chemistry combined with a poly(ethylene glycol) (PEG) spacer was used to immobilize a diverse group of biomolecules onto a solid surface. Briefly, α, ω linear PEG conjugates were synthesized containing cyclopentadiene in the α position and either biotin, lactose, or protein A in the ω position. Linkers were coupled to N -maleimide (EMC)-functionalized glass substrates, and surface immobilization of biomolecules was confirmed by confocal fluorescence imaging.
| Original language | American English |
|---|---|
| Journal | Tetrahedron Letters |
| Volume | 49 |
| DOIs | |
| State | Published - Apr 14 2008 |
Keywords
- Diels–Alder reaction; Chemical selective immobilization; Poly(ethylene glycol)
- Biomolecule
Disciplines
- Medicinal-Pharmaceutical Chemistry
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