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1.
Org Biomol Chem ; 16(20): 3726-3731, 2018 05 23.
Artículo en Inglés | MEDLINE | ID: mdl-29565089

RESUMEN

Two fluorescent dyes covalently attached in diagonal interstrand orientation to siRNA undergo energy transfer and thereby enable a dual color fluorescence readout (red/green) for hybridization. Three different structural variations were carried out and compared by their optical properties, including (i) the base surrogate approach with an acyclic linker as a substitute of the 2-deoxyriboside between the phosphodiester bridges, (ii) the 2'-modification of conventional ribofuranosides and (iii) the arabino-configured 2'-modification. The double stranded siRNA with the latter type of modification delivered the best energy transfer efficiency, which was explained by molecular dynamics simulations that showed that the two dyes are more flexible at the arabino-configured sugars compared to the completely stacked situation at the ribo-configured ones. Single molecule fluorescence lifetime measurements indicate their application in fluorescence cell imaging, which reveals a red/green fluorescence contrast in particular for the arabino-configured 2'-modification by the two dyes, which is key for tracking of siRNA transport into HeLa cells.


Asunto(s)
Colorantes Fluorescentes/química , Microscopía Confocal , ARN Interferente Pequeño/química , ARN Interferente Pequeño/metabolismo , Secuencia de Bases , Transporte Biológico , Color , Células HeLa , Humanos , Simulación de Dinámica Molecular , Conformación de Ácido Nucleico , ARN Interferente Pequeño/genética
2.
J Phys Chem B ; 123(8): 1770-1779, 2019 02 28.
Artículo en Inglés | MEDLINE | ID: mdl-30706705

RESUMEN

TisB is a short amphiphilic α-helical peptide from Escherichia coli that induces a breakdown of the pH gradient across the inner membrane when the bacteria are under stress and require to form persister cells to turn into a biofilm. A computational-experimental approach combining all-atom and coarse-grained molecular dynamics simulation with circular dichroism spectroscopy and gel electrophoresis was used to reveal its structure and oligomeric assembly in a phospholipid bilayer. TisB is found to be inserted upright in the membrane as a tetrameric bundle with a left-handed sense of supercoiling, best described as an antiparallel dimer-of-dimers. The tetramer is stabilized by means of a regular but dynamically interchanging pattern of salt bridges and hydrogen bonds, in accordance with the recently proposed "charge-zipper" motif.


Asunto(s)
Toxinas Bacterianas/química , Membrana Celular/metabolismo , Proteínas de Escherichia coli/química , Simulación de Dinámica Molecular , Multimerización de Proteína , Toxinas Bacterianas/metabolismo , Proteínas de Escherichia coli/metabolismo , Conformación Proteica en Hélice alfa
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