A Label-Free Multitechnique Approach to Characterize the Interaction of Bioactive Compounds with Biomimetic Interfaces

被引:1
作者
Fernandes, Eduarda [1 ]
Costa, Rui R. [2 ,3 ]
Machado, Raul [4 ,5 ]
Reis, Rui L. [2 ,3 ]
Pashkuleva, Iva [2 ,3 ]
Lucio, Marlene [1 ,6 ]
机构
[1] Univ Minho, Ctr Fis Univ Minho & Porto, CF UM UP, P-4710057 Braga, Portugal
[2] Univ Minho, Headquarters European Inst Excellence Tissue Engn, I3Bs Res Inst Biomat Biodegradables & Biomimet, 3Bs Res Grp, AvePk,Parque Ciencia & Tecnol, P-4805017 Braga, Portugal
[3] ICVS 3Bs, PT Govt Associate Lab, P-4805017 Braga, Portugal
[4] Univ Minho, CBMA Ctr Biol Mol & Ambiental, Aquat Res Network ARNET Associate Lab, P-4710057 Braga, Portugal
[5] Univ Minho, IB S Inst Sci & Innovat Biosustainabil, Campus Gualtar, P-4710057 Braga, Portugal
[6] Univ Minho, CBMA Ctr Biol Mol & Ambiental, P-4710057 Braga, Portugal
来源
SMALL SCIENCE | 2024年 / 4卷 / 04期
基金
美国国家科学基金会;
关键词
biomimetic models; label-free interaction characterizations; quartz-crystal microbalances; small and wide-angle X-Ray scattering; supported lipid bilayers; surface plasmon resonances; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; QUARTZ-CRYSTAL MICROBALANCE; 1,2-DIMYRISTOYL-SN-GLYCERO-3-PHOSPHOCHOLINE DMPC LIPOSOMES; SURFACE-PLASMON RESONANCE; SUPPORTED LIPID-BILAYERS; PHASE-TRANSITIONS; IN-VITRO; INFRARED-SPECTROSCOPY; BIOPHYSICAL APPROACH; MOLECULAR PARTITION;
D O I
10.1002/smsc.202300271
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Extensive research has been conducted on biomimetic interfaces mimicking the complex and diverse microenvironment of cell membranes to gain insights into bioactive compound interactions and membrane biophysics modulation. The present study proposes an innovative approach that combines five prospective label-free methodologies (derivative spectroscopy, synchrotron small- and wide-angle X-Ray scattering, attenuated total reflection-Fourier-transform infrared spectroscopy, quartz-crystal microbalance with dissipation, and surface plasmon resonance) to showcase their synergistic capabilities and complementarity in investigating drug-membrane interactions. This multitechnique approach combines the real-time monitoring of the adsorption process under continuous flow conditions with the steady-state perspective of this process. As a proof of concept, the interaction of three bioactive compounds (caffeine, testosterone, and diclofenac) with two biomimetic membrane interfaces (multistacked lipid bilayers and supported lipid bilayers) mimicking the more ordered lipid transient phases, with and without cholesterol (lo and so), that are responsible for a variety of membrane-associated biological activities, is investigated. The biophysical effects of the bioactives are discussed using complementary data from real-time and steady-state experiments, including membrane adsorption and distribution, predicted location, and induced changes in order and fluidity, encompassing bilayer thickness, hydration, and area per lipid molecule. This work introduces a label-free multitechnique approach to explore the biophysics underlying the interactions between bioactives and biomimetic models of the often-overlooked solid- and liquid-ordered phases. The combination of real-time continuous flow with equilibrium steadystate techniques was successful in providing comprehensive molecular insight into drug-membrane interactions while overcoming the limitations of conventional fluorescence-based techniques.image (c) 2024 WILEY-VCH GmbH
引用
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页数:16
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