dc.contributor.authorLi, Xuesong
dc.contributor.authorWang, Rong
dc.contributor.authorTang, Chuyang Y.
dc.contributor.authorVararattanavech, Ardcharaporn
dc.contributor.authorZhao, Yang
dc.contributor.authorTorres, Jaume
dc.contributor.authorFane, Anthony Gordon
dc.date.accessioned2013-06-27T06:06:30Z
dc.date.available2013-06-27T06:06:30Z
dc.date.copyright2012en_US
dc.date.issued2012
dc.identifier.citationLi, X., Wang, R., Tang, C., Vararattanavech, A., Zhao, Y., Torres, J., et al. (2012). Preparation of supported lipid membranes for aquaporin Z incorporation. Colloids and Surfaces B: Biointerfaces, 94, 333-340.en_US
dc.identifier.issn0927-7765en_US
dc.identifier.urihttp://hdl.handle.net/10220/10801
dc.description.abstractThere has been a recent surge of interest to mimic the performance of natural cellular membranes by incorporating water channel proteins-aquaporins (AQPs) into various ultrathin films for water filtration applications. To make biomimetic membranes one of the most crucial steps is preparing a defect-free platform for AQPs incorporation on a suitable substrate. In this study two methods were used to prepare supported lipid membranes on NF membrane surfaces under a benign pH condition of 7.8. One method was direct vesicle fusion on a hydrophilic membrane NF-270; the other was vesicle fusion facilitated by hydraulic pressure on a modified hydrophilic NF-270 membrane whose surface has been spin-coated with positively charged lipids. Experiments revealed that the supported lipid membrane without AQPs prepared by the spin coating plus vesicle fusion had a much lower defect density than that prepared by vesicle fusion alone. It appears that the surface roughness and charge are the main factors determining the quality of the supported lipid membrane. Aquaporin Z (AqpZ) proteins were successfully incorporated into 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) liposomes and its permeability was measured by the stopped-flow experimental procedure. However, after the proteoliposomes have been fused onto the modified substrate, the AqpZ function in the resultant membrane was not observed and AFM images showed distinct aggregations of unfused proteoliposomes or AqpZ proteins on the substrate surface. It is speculated that the inhibition of AqpZ function may be caused by the low lipid mobility on the NF membrane surface. Further investigations to evaluate and optimize the structure-performance relationship are required.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesColloids and surfaces B : biointerfacesen_US
dc.rights© 2012 Elsevier B.V.en_US
dc.titlePreparation of supported lipid membranes for aquaporin Z incorporationen_US
dc.typeJournal Article
dc.contributor.researchSingapore Membrane Technology Centreen_US
dc.contributor.schoolSchool of Civil and Environmental Engineeringen_US
dc.contributor.schoolSchool of Biological Sciencesen_US
dc.identifier.doihttp://dx.doi.org/10.1016/j.colsurfb.2012.02.013


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