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Interaction of cysteine and its derivatives with monolayers of dipalmitoylphosphatidylcholine.
Arias, J M; Díaz, S B; Ben Altabef, A; Dupuy, F G.
  • Arias JM; INQUINOA-CONICET-UNT, Instituto de Química Física, Facultad de Bioquímica, Química y Farmacia, Universidad Nacional de Tucumán, San Lorenzo 456, T4000CAN San Miguel de Tucumán, Argentina.
  • Díaz SB; Instituto de Química Física, Facultad de Bioquímica, Química y Farmacia, Universidad Nacional de Tucumán (UNT), San Lorenzo 456, T4000CAN Tucumán, Argentina.
  • Ben Altabef A; Instituto de Química Física, Facultad de Bioquímica, Química y Farmacia, Universidad Nacional de Tucumán (UNT), San Lorenzo 456, T4000CAN Tucumán, Argentina; INQUINOA-CONICET-UNT, Instituto de Química Física, Facultad de Bioquímica, Química y Farmacia, Universidad Nacional de Tucumán, San Lorenzo 45
  • Dupuy FG; Instituto Superior de Investigaciones Biológicas (INSIBIO), CONICET-UNT and Instituto de Química Biológica "Dr. Bernabé Bloj", Facultad de Bioquímica, Química y Farmacia, UNT, Chacabuco 461, T4000ILI Tucumán, Argentina. Electronic address: fdupuy@fbqf.unt.edu.ar.
Colloids Surf B Biointerfaces ; 184: 110548, 2019 Dec 01.
Article en En | MEDLINE | ID: mdl-31614252
ABSTRACT
Molecular interactions between l-cysteine (Cys) and its ester derivatives (Cysx); l-cysteine ethyl ester (CE), l-cysteine methyl ester (CM) and N-acetyl l-cysteine (NAC) with 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) monolayers were investigated using Langmuir film balance technique. The effect of charge on monolayers made of cysteine and three ester derivatives with DPPC was investigated by working with un-buffered and buffered subphases. Also, the effects of cysteine derivatives interaction with DPPC monolayers were studied measuring the change in the surface tension upon aminoacid injection in the subphase whilst keeping lipid molecular density and lateral packing controlled. Cysteine and its ester derivatives showed interfacial activity reducing the air/water surface tension (πi) by 4 mN m-1. However, ester derivatives were able to insert into preformed DPPC monolayers at much higher surface pressures (Δπ), indicating a preferential interaction of Cysx with DPPC. The results indicate that, although the different derivatives of cysteine presented low surface activity, they were able to favourably interact with DPPC monolayers. Also, compression isotherms experiments in binary mixtures indicate that the more surface active compounds stabilized the gel phase of DPPC. The charge on cysteine and its derivatives did not increase the observed effects.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: 1,2-Dipalmitoilfosfatidilcolina / Cisteína Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: 1,2-Dipalmitoilfosfatidilcolina / Cisteína Idioma: En Año: 2019 Tipo del documento: Article