TY - CHAP
T1 - Synthesis of chain-end functionalized glycopolymers via cyanoxyl-mediated free radical polymerization (Cmfrp)
AU - Gruzdys, Valentinas
AU - Tang, Jinshan
AU - Chaikof, Elliot
AU - Sun, Xue
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Glycopolymers are often used as glyco-macroligands for biological research and biomedical applications in carbohydrate recognitions. Chain-end functionalized glycopolymers show more potential for practical applications, such as protein modification and solid-phase bioassays. In particular, the chain-end group allows for direct one-to-one attachment or facilitates site-specifi c and oriented immobilization onto solid surfaces. A series of derivatized arylamine initiators are used to generate chain-end functionalized glycopolymers by cyanoxyl-mediated free radical polymerization (CMFRP). Important features of this strategy include the capacity to produce polymers of low polydispersity (PDI <1.5) under aqueous conditions using unprotected monomers bearing a wide range of functional groups. In addition, it provides a one-pot method to synthesize α, ω-telechelic glycopolymers with derivatized arylamine at one site and O -cyanate at the other site. In the process, the capacity to orthogonally label glycopolymers or otherwise conjugate them to proteins and other molecules is greatly enhanced.
AB - Glycopolymers are often used as glyco-macroligands for biological research and biomedical applications in carbohydrate recognitions. Chain-end functionalized glycopolymers show more potential for practical applications, such as protein modification and solid-phase bioassays. In particular, the chain-end group allows for direct one-to-one attachment or facilitates site-specifi c and oriented immobilization onto solid surfaces. A series of derivatized arylamine initiators are used to generate chain-end functionalized glycopolymers by cyanoxyl-mediated free radical polymerization (CMFRP). Important features of this strategy include the capacity to produce polymers of low polydispersity (PDI <1.5) under aqueous conditions using unprotected monomers bearing a wide range of functional groups. In addition, it provides a one-pot method to synthesize α, ω-telechelic glycopolymers with derivatized arylamine at one site and O -cyanate at the other site. In the process, the capacity to orthogonally label glycopolymers or otherwise conjugate them to proteins and other molecules is greatly enhanced.
KW - Biotin
KW - Carbohydrate
KW - Chain-end functionalized
KW - Cyanoxyl-mediated free radical polymerization
KW - Glycopolymer
KW - Lactose
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84946429880&origin=inward
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=84946429880&origin=inward
U2 - 10.1007/978-1-4939-3130-9_1
DO - 10.1007/978-1-4939-3130-9_1
M3 - Chapter
C2 - 26537460
VL - 1367
T3 - Methods in Molecular Biology
SP - 3
EP - 12
BT - Methods in Molecular Biology
PB - Humana Press [email protected]
CY - usa
ER -