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H. Ge, “UPA, a Universal Protein Array System for Quantitative Detection of Protein-Protein, Protein-DNA, Protein-RNA and Protein-Ligand Interactions,” Nucleic Acid Research, Vol. 28, No. 2, 2000, p. e3. doi:10.1093/nar/28.2.e3

has been cited by the following article:

• TITLE: Immobilization of His-Tagged Proteins on Various Solid Surfaces Using NTA-Modified Chitosan

  AUTHORS: Masahiko Oshige, Kazuhiro Yumoto, Hidefumi Miyata, Shunsuke Takahashi, Masaki Nakada, Kanako Ito, Miwa Tamegai, Hiroki Kawaura, Shinji Katsura

  KEYWORDS: Protein Immobilization; Chitosan; Ni-NTA (Nickel-Nitrilotriacetic Acid); Solid Surface

  JOURNAL NAME: Open Journal of Polymer Chemistry, Vol.3 No.1, February 28, 2013

  ABSTRACT: Continued advancement of protein array, bioelectrode, and biosensor technologies will necessitate development of methods that allow for increased protein immobilization capacity and more control over protein orientation. Toward these ends, we developed a method involving modification of chitosan with nitrilotriacetic acid (NTA) to achieve immobilization of a larger amount of His-tagged protein than is possible with current methods. The immobilization capacity of our method was evaluated using His-tagged GFP (Green Fluorescent Protein) as a model protein. The average immobilization density on modified glass was about 32 ng/mm2. Our method is suitable for use on a variety of solid surfaces, including glassy carbon, silicon wafers, polycarbonate, and beaten gold.