TY - JOUR
T1 - Peptide-Membrane Interactions Monitored by Fluorescence Lifetime Imaging
T2 - A Study Case of Transportan 10
AU - Anselmo, Sara
AU - Sancataldo, Giuseppe
AU - Mørck Nielsen, Hanne
AU - Foderà, Vito
AU - Vetri, Valeria
N1 - Funding Information:
The authors thank the University of Palermo for financial support (FFR─PROMETA project). Part of microscopy was performed at the Advanced Technologies Network (ATeN) Center, University of Palermo. G.S. has received funding from PON AIM1809078-1.
Publisher Copyright:
©
PY - 2021
Y1 - 2021
N2 - The interest on detailed analysis of peptide-membrane interactions is of great interest in both fundamental and applied sciences as these may relate to both functional and pathogenic events. Such interactions are highly dynamic and spatially heterogeneous, making the investigation of the associated phenomena highly complex. The specific properties of membranes and peptide structural details, together with environmental conditions, may determine different events at the membrane interface, which will drive the fate of the peptide-membrane system. Here, we use an experimental approach based on the combination of spectroscopy and fluorescence microscopy methods to characterize the interactions of the multifunctional amphiphilic peptide transportan 10 with model membranes. Our approach, based on the use of suitable fluorescence reporters, exploits the advantages of phasor plot analysis of fluorescence lifetime imaging microscopy measurements to highlight the molecular details of occurring membrane alterations in terms of rigidity and hydration. Simultaneously, it allows following dynamic events in real time without sample manipulation distinguishing, with high spatial resolution, whether the peptide is adsorbed to or inserted in the membrane.
AB - The interest on detailed analysis of peptide-membrane interactions is of great interest in both fundamental and applied sciences as these may relate to both functional and pathogenic events. Such interactions are highly dynamic and spatially heterogeneous, making the investigation of the associated phenomena highly complex. The specific properties of membranes and peptide structural details, together with environmental conditions, may determine different events at the membrane interface, which will drive the fate of the peptide-membrane system. Here, we use an experimental approach based on the combination of spectroscopy and fluorescence microscopy methods to characterize the interactions of the multifunctional amphiphilic peptide transportan 10 with model membranes. Our approach, based on the use of suitable fluorescence reporters, exploits the advantages of phasor plot analysis of fluorescence lifetime imaging microscopy measurements to highlight the molecular details of occurring membrane alterations in terms of rigidity and hydration. Simultaneously, it allows following dynamic events in real time without sample manipulation distinguishing, with high spatial resolution, whether the peptide is adsorbed to or inserted in the membrane.
U2 - 10.1021/acs.langmuir.1c02392
DO - 10.1021/acs.langmuir.1c02392
M3 - Journal article
C2 - 34714654
AN - SCOPUS:85118797590
VL - 37
SP - 13148
EP - 13159
JO - Langmuir
JF - Langmuir
SN - 0743-7463
IS - 44
ER -