Infrared Spectroscopic Study of Multi-Component Lipid Systems: A Closer Approximation to Biological Membrane Fluidity

被引:11
作者
Klaiss-Luna, Maria C. [1 ]
Manrique-Moreno, Marcela [1 ]
机构
[1] Univ Antioquia, Fac Exact & Nat Sci, Chem Inst, AA 1226, Medellin 050010, Colombia
关键词
lipid model membranes; supported lipid bilayers; LL-37; thermal behavior; membrane fluidity; infrared spectroscopy; ANTIMICROBIAL PEPTIDE LL-37; PHASE-BEHAVIOR; CELL-MEMBRANES; HEADGROUP STRUCTURE; CHAIN-LENGTH; MODEL; BILAYER; PHOSPHATIDYLSERINE; PHOSPHOLIPIDS; ORGANIZATION;
D O I
10.3390/membranes12050534
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Membranes are essential to cellular organisms, and play several roles in cellular protection as well as in the control and transport of nutrients. One of the most critical membrane properties is fluidity, which has been extensively studied, using mainly single component systems. In this study, we used Fourier transform infrared spectroscopy to evaluate the thermal behavior of multi-component supported lipid bilayers that mimic the membrane composition of tumoral and non-tumoral cell membranes, as well as microorganisms such as Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus. The results showed that, for tumoral and non-tumoral membrane models, the presence of cholesterol induced a loss of cooperativity of the transition. However, in the absence of cholesterol, the transitions of the multi-component lipid systems had sigmoidal curves where the gel and fluid phases are evident and where main transition temperatures were possible to determine. Additionally, the possibility of designing multi-component lipid systems showed the potential to obtain several microorganism models, including changes in the cardiolipin content associated with the resistance mechanism in Staphylococcus aureus. Finally, the potential use of multi-component lipid systems in the determination of the conformational change of the antimicrobial peptide LL-37 was studied. The results showed that LL-37 underwent a conformational change when interacting with Staphylococcus aureus models, instead of with the erythrocyte membrane model. The results showed the versatile applications of multi-component lipid systems studied by Fourier transform infrared spectroscopy.
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页数:13
相关论文
共 72 条
[1]   Vesicles mimicking normal and cancer cell membranes exhibit differential responses to the cell-penetrating peptide Pep-1 [J].
Almarwani, Bashiyar ;
Phambu, Esther Nzuzi ;
Alexander, Christopher ;
Nguyen, Ha Aimee T. ;
Phambu, Nsoki ;
Sunda-Meya, Anderson .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES, 2018, 1860 (06) :1394-1402
[2]  
Aloia R.C., 2013, Membrane Fluidity in Biology: Disease Processes
[3]   Liposomes as biomembrane models: Biophysical techniques for drug-membrane interaction studies [J].
Andrade, Stephanie ;
Ramalho, Maria J. ;
Loureiro, Joana A. ;
Pereira, Maria Carmo .
JOURNAL OF MOLECULAR LIQUIDS, 2021, 334
[4]   Phase behavior of palmitoyl and egg sphingomyelin [J].
Arsov, Zoran ;
Gonzalez-Ramirez, Emilio J. ;
Goni, Felix M. ;
Tristram-Nagle, Stephanie ;
Nagle, John F. .
CHEMISTRY AND PHYSICS OF LIPIDS, 2018, 213 :102-110
[5]   Updates on the pathogenicity status of Pseudomonas aeruginosa [J].
Azam, Mohd W. ;
Khan, Asad U. .
DRUG DISCOVERY TODAY, 2019, 24 (01) :350-359
[6]   Hydration of phospholipid bilayers in the presence and absence of cholesterol [J].
Bach, D ;
Miller, IR .
CHEMISTRY AND PHYSICS OF LIPIDS, 2005, 136 (01) :67-72
[7]  
Bagatolli LA, 1999, PHOTOCHEM PHOTOBIOL, V70, P557, DOI 10.1562/0031-8655(1999)070<0557:AMFTIO>2.3.CO
[8]  
2
[9]  
Bergman P, 2007, CURR HIV RES, V5, P410
[10]   Erythrocyte membrane fluidity as a marker of diabetic retinopathy in type 1 diabetes mellitus [J].
Bianchetti, Giada ;
Viti, Luca ;
Scupola, Andrea ;
Di Leo, Mauro ;
Tartaglione, Linda ;
Flex, Andrea ;
De Spirito, Marco ;
Pitocco, Dario ;
Maulucci, Giuseppe .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2021, 51 (05)