Utilizing adsorbed proteoliposomes trapped in a non-ruptured state on SiO2 for amplified detection of membrane proteins
Journal article, 2004

The quartz crystal microbalance with dissipation (QCM-D) technique was used to monitor the formation of supported phospholipid bilayers (SPBs) on SiO2 using proteoliposomes with reconstituted proton translocating nicotinamide nucleotide transhydrogenase (TH). Exposure of the surface to such proteoliposomes creates a lipid film composed of a mixture of proteolipid bilayers and adsorbed non-ruptured proteoliposomes, where the fraction of the latter is reduced if the TH-liposomes are pretreated with trypsin to remove the water soluble domains of TH [Langmuir 19 (2003) 842]. In the present work, the latter study is complemented by investigating the influence of trypsin treatment of the mixed adlayer (proteolipid bilayer + non-ruptured proteoliposomes) after adsorption on the surface. This demonstrates how trypsin-cleavage induced rupture of adsorbed TH-liposomes can be utilized to detect the presence of less than 0.04 pmol/cm2 of immobilized TH.




Transmembrane proteins

Supported membranes


Annette Granéli

Chalmers, Applied Physics

Jan Rydström

University of Gothenburg

Bengt Herbert Kasemo

Chalmers, Applied Physics, Chemical Physics

Fredrik Höök

Chalmers, Applied Physics, Chemical Physics

Biosensors and Bioelectronics

0956-5663 (ISSN)

Vol. 20 3 498-504

Subject Categories

Biochemistry and Molecular Biology

Physical Sciences





More information