Premium
Cobalt(III)‐Mediated Permanent and Stable Immobilization of Histidine‐Tagged Proteins on NTA‐Functionalized Surfaces
Author(s) -
Wegner Seraphine V.,
Schenk Franziska C.,
Spatz Joachim P.
Publication year - 2016
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201504465
Subject(s) - nitrilotriacetic acid , imidazole , chemistry , cobalt , ethylenediaminetetraacetic acid , histidine , combinatorial chemistry , monolayer , chelation , thiol , organic chemistry , biochemistry , enzyme
We present the cobalt(III)‐mediated interaction between polyhistidine (His)‐tagged proteins and nitrilotriacetic acid (NTA)‐modified surfaces as a general approach for a permanent, oriented, and specific protein immobilization. In this approach, we first form the well‐established Co 2+ ‐mediated interaction between NTA and His‐tagged proteins and subsequently oxidize the Co 2+ center in the complex to Co 3+ . Unlike conventionally used Ni 2+ ‐ or Co 2+ ‐mediated immobilization, the resulting Co 3+ ‐mediated immobilization is resistant toward strong ligands, such as imidazole and ethylenediaminetetraacetic acid (EDTA), and washing off over time because of the high thermodynamic and kinetic stability of the Co 3+ complex. This immobilization method is compatible with a wide variety of surface coatings, including silane self‐assembled monolayers (SAMs) on glass, thiol SAMs on gold surfaces, and supported lipid bilayers. Furthermore, once the cobalt center has been oxidized, it becomes inert toward reducing agents, specific and unspecific interactions, so that it can be used to orthogonally functionalize surfaces with multiple proteins. Overall, the large number of available His‐tagged proteins and materials with NTA groups make the Co 3+ ‐mediated interaction an attractive and widely applicable platform for protein immobilization.