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Zhen, G., Eggli, V., V?r?s, J., Zammaretti, P., Textor, M., Glockshuber, R. and Kuennemann, E. (2004) Immobilization of the enzyme beta-lactamase on biotin- derivatized poly(L-lysine)-g-poly(ethylene glycol)-coated sensor chips: a study on oriented attachment and surface activity by enzyme kinetics and in situ optical sensing. Langmuir, 20, 10464-10473. doi:10.1021/la0482812

has been cited by the following article:

• TITLE: Immobilization of antibodies on the self-assembled monolayer by antigen-binding site protection and immobilization kinetic control

  AUTHORS: Myungok Yoon, Hyun Jin Hwang, Jeong Hee Kim

  KEYWORDS: Antibody; Oriented Immobilization; Antigen-Binding Site Protection; Self-Assembled Monolayer; Kinetic Control

  JOURNAL NAME: Journal of Biomedical Science and Engineering, Vol.4 No.4, April 20, 2011

  ABSTRACT: The orientation of the biological molecule immobi-lized on a solid surface has been critical in devel-opment of various applications. In this study, ori-entation of antibody was retained by protecting the antigen-binding site of the antibody prior to immo-bilization to -functionalized mixed self-assembled monolayer (SAM) of 12-mercaptododecanoic acid and 1-heptanethiol. More importantly, the number of immobilization bonds formed between each an-tigen-binding site protected antibody molecule and the solid surface was controlled by optimizing the mole fraction of the activated carboxyl group of the linker molecules in the mixed SAM. The amount of antibody used in this study was approximately equivalent to the amount for one monolayer surface coverage. The resulting activity of protected immo-bilized antibody was about 10 fold higher than that of random immobilized antibody