| Literature DB >> 29956230 |
Zhengjian Lv1,2, Siddhartha Banerjee1, Karen Zagorski1, Yuri L Lyubchenko3.
Abstract
Nanoimaging methods, atomic force microscopy (AFM) in particular, are widely used to study the interaction of biological molecules with the supported lipid bilayer (SLB), which itself is a traditional model for cellular membranes. Success in these studies is based on the availability of a stable SLB for the required observation period, which can extend several hours. The application of AFM requires that the SLB have a smooth morphology, thus enabling visualization of proteins and other molecules on its surface. Herein, we describe protocols for SLB assembly by using 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) and 1-palmitoyl-2-oleoyl-sn-glycero-3-phospho-L-serine (POPS) on a mica support. Our methodology enables us to assemble defect-free POPC and POPS SLBs that remain stable for at least 8 h. The application of such smooth and stable surfaces is illustrated by monitoring of the on-surface aggregation of amyloid proteins with the use of time-lapse AFM.Entities:
Keywords: Amyloid aggregation; Atomic force microscope; Nanoimaging; Supported lipid bilayer; Time-lapse imaging
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Year: 2018 PMID: 29956230 PMCID: PMC6045422 DOI: 10.1007/978-1-4939-8591-3_8
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745