Covalently immobilised cytochrome c imaged by in situ scanning tunnelling microscopy

Jens E.T. Andersen, Klaus G. Olesen, Alexey I. Danilov, Carl E. Foverskov, Per Møller, Jens Ulstrup

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21 Citations (Scopus)

Abstract

In situ scanning tunnelling microscopy (STM) imaging of cytochrome c (cyt c) on polycrystalline Pt surfaces and on Au(111) was achieved first by covalent immobilisation of 3-aminopropyltriethoxysilane (3-APTS) brought to react with oxide present on the Pt surfaces. Covalently bound 3-APTS forms a further link to glutaric dialdehyde which immobilises the protein molecules. Cyt c is immobilised on Au(111) by reaction with N-acetylcystein and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide. Imaging by in situ STM in a 20 mM phosphate buffer electrolyte with a Au/AuO(x) reference electrode could then be achieved. Protein was identified as hemispherical features on the surface with close to molecular resolution and with a quite different character compared both to the bare metal surfaces and to metal surfaces with only linker molecules attached. No subunits or side chains were visible, but the protein exhibited a grained surface appearance, possibly caused by mobile subunits or immobilising agent.

Original languageEnglish
Pages (from-to)57-63
Number of pages7
JournalBioelectrochemistry and Bioenergetics
Volume44
Issue number1
DOIs
Publication statusPublished - Nov 1 1997

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All Science Journal Classification (ASJC) codes

  • Biochemistry

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