Proteo-lipobeads to encapsulate cytochrome c oxidase from Paracoccus denitrificans

Andreas Geiss, Christina Bliem, Pinar Frank, C Reiner-Rozman, Justin Kewney, Michael Boersch, Renate L. C. Naumann

Research output: Contribution to journalArticlepeer-review

Abstract

Proteo-lipobeads (PLBs) are investigated as cell-free model systems to encapsulate membrane proteins such as ion channels and transporters. PLBs are based on nickel nitrile tri-acetic acid (Ni-NTA)- functionalized agarose beads, onto which membrane proteins (MP) are bound via histidine(his)-tag. Composite beads thus obtained (subsequently called proteobeads) are dialyzed in the presence of lipid micelles to form PLBs. As an example we employed cytochrome c oxidase from P. denitrificans with a his-tag fused to the C-terminus of subunit I. In this orientation the P side of CcO faces the outside of the PLB and hence protons are released to the outer aqueous phase, when electron transfer is initiated by light excitation of Ru complexes. Proton release kinetics was probed by fluorescence microscopy using the pH-sensitive sensor molecule fluorescein DHPE inserted into the lipid layer. In order to monitor the generation of membrane potentials we performed a FLIPR assay on the CcO embedded in PLBs using the FRET pair CC2-DMPE/DiSBAC2(3). The combined results show that PLBs can be used as a model system
Original languageEnglish
Pages (from-to)119-125
Number of pages7
JournalJournal of Colloid & Interface Science
Volume500
DOIs
Publication statusPublished - 2017

Research Field

  • Biosensor Technologies

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