Inhibition of LPS-induced nitric oxide production by transduced Tat-arginine deiminase fusion protein in Raw 264.7 cells

  • Lee, Min Jung; 
  • Kim, Dae Won; 
  • Lee, Yeom Pyo; 
  • Jeong, Hoon Jae; 
  • Kang, Hye Won; 
  • ... Min, Bon-Hong; 
  • 외 11명
Citations

WEB OF SCIENCE

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SCOPUS

3

초록

Arginine deiminase (ADI), an arginine-degrading enzyme, has anti-proliferative and anti-tumor activities and is capable of inhibiting the production of nitric oxide (NO). Modulation of nitric oxide (NO) production is considered a promising approach for the treatment of various diseases including cancer, inflammation and neuronal disorders. In this study, an ADI gene was fused with an HIV-1 Tat peptide in a bacterial expression vector to produce an genetic in-frame Tat-ADI fusion protein. When added exogenously to the culture media, the expressed and purified Tat-ADI fusion proteins were efficiently transduced into macrophage Raw 264.7 cells in a time- and dose-dependent manner. Furthermore, transduced Tat-ADI fusion proteins markedly increased cell viability in cells treated with lipopolysaccharide (LPS). This increase in viability was mediated by an inhibition of NO production. These results suggest that this Tat-ADI fusion protein can be used in protein therapies of NO-related disorders such as cancer, inflammation and neuronal diseases. [BMB reports 2009; 42(5): 286-292]

키워드

Arginine deiminase (ADI); HIV-1 Tat peptide; Inflammation; Nitric oxide synthase; Protein transduction; CU,ZN-SUPEROXIDE DISMUTASE; EFFICIENTLY PROTECTS; IN-VITRO; MICE; NEUROTOXICITY; ASPARAGINASE; RESISTANCE; DEFICIENT; MECHANISM; DELIVERY
제목
Inhibition of LPS-induced nitric oxide production by transduced Tat-arginine deiminase fusion protein in Raw 264.7 cells
저자
Lee, Min Jung; Kim, Dae Won; Lee, Yeom Pyo; Jeong, Hoon Jae; Kang, Hye Won; Shin, Min Jae; Sohn, Eun Jeong; Kim, Mi Jin; Jang, Sang Ho; Kang, Tae-Cheon; Won, Moo Ho; Min, Bon-Hong; Cho, Sung-Woo; Lee, Kil Soo; Park, Jinseu; Eum, Won Sik; Choi, Soo Young
DOI
10.5483/BMBRep.2009.42.5.286
발행일
2009-05-31
유형
Article
저널명
BMB Reports
권
42
호
5
페이지
286 ~ 292