One of the central issues facing the emerging field of nanotechnology is cellular compatibility. Nanoparticles have been proposed for diagnostic and therapeutic applications, including drug delivery, gene therapy, biological sensors, and controlled catalysis. Viruses, liposomes, peptides, and synthetic and natural polymers have been engineered for these applications, yet significant limitations continue to prevent their use. Avoidance of the body's natural immune system, lack of targeting specificity, and the inability to control packaging and release are remaining obstacles. We have explored the use of a naturally occurring cellular nanoparticle known as the vault, which is named for its morphology with multiple arches reminiscent of cathedral ceilings. Vaults are 13-MDa ribonucleoprotein particles with an internal cavity large enough to sequester hundreds of proteins. Here, we report a strategy to target and sequester biologically active materials within the vault cavity. Attachment of a vault-targeting peptide to two proteins, luciferase and a variant of GFP, resulted in their sequestration within the vault cavity. The targeted proteins confer enzymatic and fluorescent properties on the recombinant vaults, both of which can be detected by their emission of light. The modified vaults are compatible with living cells. The ability to engineer vault particles with designed properties and functionalities represents an important step toward development of a biocompatible nanocapsule.capsule ͉ nanoparticle

Mesostructured silica thin films and particles prepared by surfactant‐templated sol–gel techniques are highly versatile substrates for the formation of functional materials. The ability to deliberately place molecules possessing desired activities in specific spatially separated regions of the nanostructure is an important feature of these materials. Such placement utilizes strategies that exploit the physical and chemical differences between the silica framework and the templated pores. As an example of placement of pairs of molecules, donor and acceptor molecules can be targeted to different regions of mesostructured thin films and energy transfer between them can be measured. The results not only demonstrate the spatial separation but also are used as a molecular ruler to measure the average distance between them. Mesostructured silica is also an excellent support for molecular machines. Molecules that undergo large amplitude motion, when attached to the silica, can function as impellers and nanovalves when activated by light, electrical (redox) and chemical (pH, competitive binding) energy. Derivatized azobenzene molecules, attached to pore walls by using one of the placement strategies, function as impellers that can move other molecules through the pores. Rotaxanes and pseudorotaxanes, placed at pore entrances, function as gatekeepers that can trap and release molecules from the pores when stimulated. Deliberately placed functional molecules on and in mesostructured silica offer many possibilities for both fundamental studies on the nanoscale and for applications in fields as diverse as fluidics, biological drug delivery and controlled release.