Disorder in Order-Related Membrane Biophysical Parameters: An In-Depth Analysis of Di-4-ANEPPDHQ Generalized
Rosemary Chandrakanthi Kothalawala1, Csenge Makay1, Lajos Szente2
1Department of Biophysics and Cell Biology, Faculty of Medicine, University of Debrecen and MTA Centre of Excellence, Hungarian Academy of Sciences, Egyetem tér 1, Debrecen H-4032, Hungary.
Abstract:
Molecular order-related bulk membrane properties that substantially modulate protein functions can be examined with environment-sensitive probes, such as the prototypical and most widely applied solvatochromic Laurdan, whose spectral parameters change depending on the local hydrophobicity. Di-4-ANEPPDHQ is a widely accepted Laurdan alternative with more favorable spectral properties suitable for standard imaging, and information provided by the two fluorophores is generally considered equivalent. In our study, using fluorescence-based experimental approaches, we demonstrate that different sterols distinctly alter di-4-ANEPPDHQ spectral properties, and these changes do not correlate with those observed with Laurdan. Our molecular dynamics simulations reveal that this may be caused by their distinct depth localization in bilayers since the sensor moiety of di-4-ANEPPDHQ is localized in the vicinity of the membrane-water interface as opposed to that of Laurdan lying near the hydrophobic core. Therefore, di-4-ANEPPDHQ can be considered as a complementary tool rather than an equivalent substitute of Laurdan.
Related Concept Videos
Asymmetric Lipid Bilayer
Potential Due to a Polarized Object
Induced Electric Dipoles
Since the absolute value of potential energy holds no physical meaning, its zero value can be chosen as per...
¹³C NMR: Distortionless Enhancement by Polarization Transfer (DEPT)
π Molecular Orbitals of 1,3-Butadiene
The simplest conjugated diene is 1,3-butadiene: a four-carbon system where each carbon is sp2-hybridized and has an unhybridized p orbital that contains an unpaired electron. According to molecular orbital theory, atomic orbitals combine to form molecular orbitals such that the number...
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds


