Previous Page  10 / 16 Next Page
Information
Show Menu
Previous Page 10 / 16 Next Page
Page Background

Page 73

conferenceseries

.com

Volume 5, Issue 2 (Suppl)

Transcriptomics, an open access journal

ISSN: 2329-8936

Molecular Biology 2017

August 31-September 01, 2017

2

nd

International Conference on

August 31-September 01, 2017 Philadelphia, USA

Molecular Biology, Nucleic Acids &

Molecular Medicine

Aptamers selection methodology and strategy based on multiple modes of capillary electrophoresis

Feng Qu

Beijing Institute of Technology, China

N

ucleic acid aptamers are short, single-stranded DNA (ssDNA) or RNA molecules that are selected for binding to a

specific target. Aptamers can be used as recognition probes in biomedical, food and environment analysis. Moreover,

they have great potential in disease diagnosis and treatment, drug discovery, medicine research, as well as bioimaging, which

are expected to bring huge economic benefits. However, current aptamers application is far from satisfactory, and has not yet

been fully developed. The complicated selection process with high cost and low efficiency is one of the bottlenecks of their

application. Still universally accepted standard selection methods are not accepted. Capillary electrophoresis (CE) is one of the

most powerful methods for aptamers sieving (known as CE-SELEX), which has the advantages of fast, high resolution, low

sample consumption and smart separation modes of capillary zone electrophoresis (CZE), affinity capillary electrophoresis

(ACE) and capillary isoelectric focus (CIEF). Moreover, the binding of target and synthetic single stranded DNA (ss-DNA)

occurs in free solution, which eliminates the biases caused by stationary support and linker. Some important protein aptamers

have been successfully obtained based on CE, which greatly improves the selection efficiency. In our group, we aim at selection

strategy research of aptamers against multiple targets based on capillary electrophoresis, which has the characteristics of high

efficiency, high speed, low cost and multiple available modes. We propose selection strategies including: the availability of

randomly synthesized ssDNA libraries should be evaluated, the binding evaluation can be made based on fast CE analysis,

which provides more information to guide further selection.

qufengqu@bit.edu.cn

Transcriptomics 2017, 5:2 (Suppl)

DOI: 10.4172/2329-8936-C1-013