posted on 2007-09-01, 00:00authored byYongwon Jung, Jeong Min Lee, Hyungil Jung, Bong Hyun Chung
A versatile biolinker for efficient antibody immobilization
was prepared by site-specific coupling of protein G to DNA
oligonucleotide. This protein G−DNA conjugate ensures
the controlled immobilization of an antibody to the intended area on the surface of bioassay chips or particles,
while maintaining the activity and orientation of the bound
antibody. Streptococcus protein G tagged with a cysteine
residue at the N-terminus was chemically linked to amine-modified, single-stranded DNA. SPR analysis indicated
that the protein G−DNA conjugates sequence-specifically
bind to complementary surface-bound DNA probes. More
importantly, the resulting protein G, which is hybridized
onto the DNA surface, possesses a greater antibody/antigen binding ability than even properly oriented protein
G linked on the chip surface by chemical bonding.
Antibody targeting on glass slides could also be achieved
by using this linker system without modifying or spotting
antibodies. Moreover, the protein G−DNA conjugate
provided a simple but effective method to label DNA-functionalized gold nanoparticles with target antibodies.
The DNA-linked protein G construct introduced in this
study offers a useful strategy to manage antibody immobilization in many immunoassay systems.