Your browser doesn't support javascript.
loading
Controlling Protein Surface Orientation by Strategic Placement of Oligo-Histidine Tags.
Wasserberg, Dorothee; Cabanas-Danés, Jordi; Prangsma, Jord; O'Mahony, Shane; Cazade, Pierre-Andre; Tromp, Eldrich; Blum, Christian; Thompson, Damien; Huskens, Jurriaan; Subramaniam, Vinod; Jonkheijm, Pascal.
Afiliación
  • O'Mahony S; Department of Physics, Bernal Institute, University of Limerick , Limerick V94 T9PX, Ireland.
  • Cazade PA; Department of Physics, Bernal Institute, University of Limerick , Limerick V94 T9PX, Ireland.
  • Thompson D; Department of Physics, Bernal Institute, University of Limerick , Limerick V94 T9PX, Ireland.
  • Subramaniam V; Free University of Amsterdam , De Boelelaan 1105, 1081 HV Amsterdam, The Netherlands.
ACS Nano ; 11(9): 9068-9083, 2017 09 26.
Article en En | MEDLINE | ID: mdl-28850777
We report oriented immobilization of proteins using the standard hexahistidine (His6)-Ni2+:NTA (nitrilotriacetic acid) methodology, which we systematically tuned to give control of surface coverage. Fluorescence microscopy and surface plasmon resonance measurements of self-assembled monolayers (SAMs) of red fluorescent proteins (TagRFP) showed that binding strength increased by 1 order of magnitude for each additional His6-tag on the TagRFP proteins. All TagRFP variants with His6-tags located on only one side of the barrel-shaped protein yielded a 1.5 times higher surface coverage compared to variants with His6-tags on opposite sides of the so-called ß-barrel. Time-resolved fluorescence anisotropy measurements supported by polarized infrared spectroscopy verified that the orientation (and thus coverage and functionality) of proteins on surfaces can be controlled by strategic placement of a His6-tag on the protein. Molecular dynamics simulations show how the differently tagged proteins reside at the surface in "end-on" and "side-on" orientations with each His6-tag contributing to binding. Also, not every dihistidine subunit in a given His6-tag forms a full coordination bond with the Ni2+:NTA SAMs, which varied with the position of the His6-tag on the protein. At equal valency but different tag positions on the protein, differences in binding were caused by probing for Ni2+:NTA moieties and by additional electrostatic interactions between different fractions of the ß-barrel structure and charged NTA moieties. Potential of mean force calculations indicate there is no specific single-protein interaction mode that provides a clear preferential surface orientation, suggesting that the experimentally measured preference for the end-on orientation is a supra-protein, not a single-protein, effect.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oligopéptidos / Anémonas de Mar / Proteínas Inmovilizadas / Histidina / Proteínas Luminiscentes / Níquel / Ácido Nitrilotriacético Límite: Animals Idioma: En Revista: ACS Nano Año: 2017 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Oligopéptidos / Anémonas de Mar / Proteínas Inmovilizadas / Histidina / Proteínas Luminiscentes / Níquel / Ácido Nitrilotriacético Límite: Animals Idioma: En Revista: ACS Nano Año: 2017 Tipo del documento: Article Pais de publicación: Estados Unidos