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Ajou University

Functional stability of a nucleic acid-hydrolyzing single chain antibody in various biochemical and biophysical environments

Abstract

dc:description

3D8 single chain variable fragment (scFv) antibody has cell-penetrating activity, nucleic acid-binding activity, nucleic acid-hydrolyzing activity, and antiviral activity. As a first step toward development of antiviral reagent using 3D8 scFv, functional stability based on DNA-binding and -hydrolyzing activity of 3D8 scFv was analyzed under biochemical and biophysical conditions such as different temperature, pH, storage period, reducing environment, lyophilization, and repetitive freeze-thaw. The DNA-binding activity and -hydrolyzing activity were maintained for 6 h at 50°C. The optimal pH showing the DNA-binding activity and -hydrolyzing activity was exhibited for 2 h at pH 7-11. The DNA-binding and -hydrolyzing activity were fully retained in the presence of reducing agent, 2 mM dithiothreitol (DTT). Moreover, DNA-hydrolyzing activity of 3D8 scFv was maintained after lyophilization and 30 cycles of freeze-thaw. When the 3D8 scFv was stored in pH 3-12 for a month at 37°C, DNA-hydrolyzing activity was retained at pH 4-8. In addition, we defined the unit for DNA-hydrolyzing activity and investigated antiviral activity against influenza A virus according to the unit. Our study would provide the basic information in developing an antiviral reagent with 3D8 scFv.

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • 이, 정민
Contributors dc:contributor
  • 권, 명희
  • 대학원 의생명과학과
  • 201424106

Subjects

dc:subject × 5

Rights

Language dc:language
en

Identifiers

dc:identifier.*
OAI identifier oai:identifier
oai:repository.ajou.ac.kr:201003/13024

Chain of custody

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Harvested from
Ajou University
Base URL
repository.ajou.ac.kr/oai/request
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

이, 정민. Functional stability of a nucleic acid-hydrolyzing single chain antibody in various biochemical and biophysical environments. 2016. http://repository.ajou.ac.kr/handle/201003/13024