posted on 2013-07-09, 00:00authored byRima Budvytyte, Gintaras Valincius, Gediminas Niaura, Vladislava Voiciuk, Mindaugas Mickevicius, Hilary Chapman, Haw-Zan Goh, Prabhanshu Shekhar, Frank Heinrich, Siddharth Shenoy, Mathias Lösche, David J. Vanderah
The
self-assembled monolayers (SAMs) of new lipidic anchor molecule
HC18 [Z-20-(Z-octadec-9-enyloxy)-3,6,9,12,15,18,22-heptaoxatetracont-31-ene-1-thiol]
and mixed HC18/β-mercaptoethanol (βME) SAMs were studied
by spectroscopic ellipsometry, contact angle measurements, reflection–absorption
infrared spectroscopy, and electrochemical impedance spectroscopy
(EIS) and were evaluated in tethered bilayer lipid membranes (tBLMs).
Our data indicate that HC18, containing a double bond in the alkyl
segments, forms highly disordered SAMs up to anchor/βME molar
fraction ratios of 80/20 and result in tBLMs that exhibit higher lipid
diffusion coefficients relative to those of previous anchor compounds
with saturated alkyl chains, as determined by fluorescence correlation
spectroscopy. EIS data shows the HC18 tBLMs, completed by rapid solvent
exchange or vesicle fusion, form more easily than with saturated lipidic
anchors, exhibit excellent electrical insulating properties indicating
low defect densities, and readily incorporate the pore-forming toxin
α-hemolysin. Neutron reflectivity measurements on HC18 tBLMs
confirm the formation of complete tBLMs, even at low tether compositions
and high ionic lipid compositions. Our data indicate that HC18 results
in tBLMs with improved physical properties for the incorporation of
integral membrane proteins (IMPs) and that 80% HC18 tBLMs appear to
be optimal for practical applications such as biosensors where high
electrical insulation and IMP/peptide reconstitution are imperative.