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1.
Int J Mol Sci ; 14(2): 4066-80, 2013 Feb 18.
Artículo en Inglés | MEDLINE | ID: mdl-23429193

RESUMEN

The supramolecular assembly of proteins on surfaces has been investigated via the site-selective incorporation of a supramolecular moiety on proteins. To this end, fluorescent proteins have been site-selectively labeled with ferrocenes, as supramolecular guest moieties, via SNAP-tag technology. The assembly of guest-functionalized SNAP-fusion proteins on cyclodextrin- and cucurbit[7]uril-coated surfaces yielded stable monolayers. The binding of all ferrocene fusion proteins is specific as determined by surface plasmon resonance. Micropatterns of the fusion proteins, on patterned cyclodextrin and cucurbituril surfaces, have been visualized using fluorescence microscopy. The SNAP-fusion proteins were also immobilized on cyclodextrin vesicles. The supramolecular SNAP-tag labeling of proteins, thus, allows for the assembly of modified proteins via supramolecular host-guest interaction on different surfaces in a controlled manner. These findings extend the toolbox of fabricating supramolecular protein patterns on surfaces taking advantage of the high labeling efficiency of the SNAP-tag with versatile supramolecular moieties.

2.
Chemistry ; 18(22): 6788-94, 2012 May 29.
Artículo en Inglés | MEDLINE | ID: mdl-22511333

RESUMEN

Supramolecular assembly of proteins on surfaces and vesicles was investigated by site-selective incorporation of a supramolecular guest element on proteins. Fluorescent proteins were site-selectively labeled with bisadamantane by SNAP-tag technology. The assembly of the bisadamantane functionalized SNAP-fusion proteins on cyclodextrin-coated surfaces yielded stable monolayers. The binding of the fusion proteins is specific and occurs with an affinity in the order of 10(6) M(-1) as determined by surface plasmon resonance. Reversible micropatterns of the fusion proteins on micropatterned cyclodextrin surfaces were visualized by using fluorescence microscopy. Furthermore, the guest-functionalized proteins could be assembled out of solution specifically onto the surface of cyclodextrin vesicles. The SNAP-tag labeling of proteins thus allows for assembly of modified proteins through a host-guest interaction on different surfaces. This provides a new strategy in fabricating protein patterns on surfaces and takes advantage of the high labeling efficiency of the SNAP-tag with designed supramolecular elements.


Asunto(s)
Ciclodextrinas/química , Sustancias Macromoleculares/química , Proteínas Recombinantes de Fusión/química , Liposomas Unilamelares/química , Inmovilización , Microscopía Fluorescente , Modelos Moleculares , Datos de Secuencia Molecular , Proteínas Recombinantes de Fusión/metabolismo
3.
Adv Mater ; 26(7): 1076-80, 2014 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-24277574

RESUMEN

Dual-responsive soft matter: A soft hybrid material composed of superparamagnetic nanoparticles and cyclodextrin vesicles self-assembles in microscale linear aggregates in water in response to magnetic field as well as light.

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