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1.
Nucleic Acids Res ; 45(19): 11459-11465, 2017 Nov 02.
Artigo em Inglês | MEDLINE | ID: mdl-28977499

RESUMO

DNA serves as nature's information storage molecule, and has been the primary focus of engineered systems for biological computing and data storage. Here we combine recent efforts in DNA self-assembly and toehold-mediated strand displacement to develop a rewritable multi-bit DNA memory system. The system operates by encoding information in distinct and reversible conformations of a DNA nanoswitch and decoding by gel electrophoresis. We demonstrate a 5-bit system capable of writing, erasing, and rewriting binary representations of alphanumeric symbols, as well as compatibility with 'OR' and 'AND' logic operations. Our strategy is simple to implement, requiring only a single mixing step at room temperature for each operation and standard gel electrophoresis to read the data. We envision such systems could find use in covert product labeling and barcoding, as well as secure messaging and authentication when combined with previously developed encryption strategies. Ultimately, this type of memory has exciting potential in biomedical sciences as data storage can be coupled to sensing of biological molecules.


Assuntos
Computadores Moleculares , DNA Viral/química , Armazenamento e Recuperação da Informação/métodos , Nanoestruturas/química , Bacteriófago M13/genética , DNA Viral/genética , Eletroforese em Gel de Ágar , Reprodutibilidade dos Testes
2.
Rev Sci Instrum ; 87(8): 083705, 2016 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-27587129

RESUMO

The centrifuge force microscope (CFM) was recently introduced as a platform for massively parallel single-molecule manipulation and analysis. Here we developed a low-cost and self-contained CFM module that works directly within a commercial centrifuge, greatly improving accessibility and ease of use. Our instrument incorporates research grade video microscopy, a power source, a computer, and wireless transmission capability to simultaneously monitor many individually tethered microspheres. We validated the instrument by performing single-molecule force shearing of short DNA duplexes. For a 7 bp duplex, we observed over 1000 dissociation events due to force dependent shearing from 2 pN to 12 pN with dissociation times in the range of 10-100 s. We extended the measurement to a 10 bp duplex, applying a 12 pN force clamp and directly observing single-molecule dissociation over an 85 min experiment. Our new CFM module facilitates simple and inexpensive experiments that dramatically improve access to single-molecule analysis.


Assuntos
DNA/química , Imagem Molecular/métodos , Tecnologia sem Fio , Centrifugação/métodos , Microscopia de Vídeo/métodos , Imagem Molecular/instrumentação
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