Filipin-induced lesions in planar phospholipid bilayers imaged by atomic force microscopy

Nuno C. Santos, Evgeny Ter-Ovanesyan, Joseph A. Zasadzinski, Manuel Prieto, Miguel A.R.B. Castanho

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Filipin is a macrolide polyene with antifungal activity belonging to the same family of antibiotics as amphotericin B and nystatin. Despite the spectroscopy and electron microscopy studies of its interaction with natural membranes and membrane model systems, several aspects of its biochemical action, such as the role of membrane sterols, remain to be completely understood. We have used atomic force microscopy (AFM) to study the effect of filipin on dipalmitoylphosphatidylethanolamine bilayers in the presence and absence of cholesterol. The bilayers were prepared by Langmuir-Blodgett deposition over mica and imaged under water. It was shown that filipin- induced lesions could only be found in membranes with cholesterol. In close agreement with electron microscopy results, we have reported the presence of densely packed circular protrusions in the membrane with a mean diameter of 19 nm (corrected for convolution with AFM tip) and 0.4 nm height. Larger circular protrusions (90 nm diameter and 2.5 nm height) and doughnut-shaped lesions were also detected. These results demonstrate that filipin-induced lesions in membranes previously observed by electron microscopy are not biased by artifacts resulting from sample preparation. Filipin aggregates in aqueous solution could also be imaged for the first time. These polydisperse spherical structures were observed in samples with and without cholesterol.

Original languageEnglish (US)
Pages (from-to)1869-1873
Number of pages5
JournalBiophysical journal
Issue number4
StatePublished - Oct 1998

Bibliographical note

Funding Information:
The work of NCS, MP, and MARBC was supported by projects PECS/SAU/144/95 and PCNA/C/BIO/56/96 (Program PRAXIS XXI, Ministério da Ciência e Tecnologia, Portugal). The work of ET and JAZ was supported by the Materials Science and Engineering Research Center program of the National Science Foundation under grant OMR-96-32716 and National Institutes of Health grant GM47334. NCS also acknowledges grant BD 5935/95 from PRAXIS XXI.


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