TY - JOUR
T1 - Location, orientation and dynamics of two molecules with mitochondrial activity dissolved in anionic lyomesophase. A 2H-NMR and MD study
AU - Bahamonde-Padilla, Víctor E.
AU - Martínez-Cifuentes, Maximiliano
AU - Muñoz-Masson, Daniel
AU - Ruiz, Álvaro
AU - Ahumada, Hernán
AU - Araya-Maturana, Ramiro
AU - Soto-Delgado, Jorge
AU - Weiss-López, Boris E.
PY - 2012
Y1 - 2012
N2 - 4,4-Dimethyl-5,8-dihydroanthracene-1,9,10(4H)-trione (Q1) and 9,10-Dihydroxy-4,4-dimethyl-5,8-dihydro-1(4H)-anthracenone (Q2), two molecules that inhibit cancer cell respiration, were selectively deuterated and dissolved in an anionic discotic nematic lyotropic liquid crystal (dnllc) solution. The solution provides a magnetic field oriented anisotropic medium, where the location, average orientation and dynamics of Q1 and Q2 were examined by measuring 2H-NMR quadrupole splittings (DnQ) and 2H longitudinal relaxation times (T1). The NMR data shows that both molecules are strongly attached to the aggregate and, when dissolved, increase the alignment of the interface components with the magnetic field. However they present different average orientations. To assist with the interpretation of the experimental results, 300ns Molecular Dynamics (MD) trajectories of a bilayer model of the aggregate were calculated. The results show that both molecules spontaneously diffuse inside the bilayer, to locate in the limit between the hydrophobic core and the interface. The orientations of both molecules in the aggregate are determined by the formation of H-bonds with water.
AB - 4,4-Dimethyl-5,8-dihydroanthracene-1,9,10(4H)-trione (Q1) and 9,10-Dihydroxy-4,4-dimethyl-5,8-dihydro-1(4H)-anthracenone (Q2), two molecules that inhibit cancer cell respiration, were selectively deuterated and dissolved in an anionic discotic nematic lyotropic liquid crystal (dnllc) solution. The solution provides a magnetic field oriented anisotropic medium, where the location, average orientation and dynamics of Q1 and Q2 were examined by measuring 2H-NMR quadrupole splittings (DnQ) and 2H longitudinal relaxation times (T1). The NMR data shows that both molecules are strongly attached to the aggregate and, when dissolved, increase the alignment of the interface components with the magnetic field. However they present different average orientations. To assist with the interpretation of the experimental results, 300ns Molecular Dynamics (MD) trajectories of a bilayer model of the aggregate were calculated. The results show that both molecules spontaneously diffuse inside the bilayer, to locate in the limit between the hydrophobic core and the interface. The orientations of both molecules in the aggregate are determined by the formation of H-bonds with water.
KW - Deuterium Quadrupole Splitting
KW - Hydroquinones
KW - Longitudinal Relaxation Time
KW - Lyomesophase
KW - Quinones
UR - http://www.scopus.com/inward/record.url?scp=84873694907&partnerID=8YFLogxK
U2 - 10.4067/S0717-97072012000300021
DO - 10.4067/S0717-97072012000300021
M3 - Article
AN - SCOPUS:84873694907
SN - 0717-9324
VL - 57
SP - 1295
EP - 1300
JO - Journal of the Chilean Chemical Society
JF - Journal of the Chilean Chemical Society
IS - 3
ER -