Title :
Enhances the transdcution efficiency of Tat-catalase protein attenuate neuronal cell damage
Author :
Sohn, Eun Jeong ; Kim, Mi Jin ; Ahn, Eun Hee ; Kwon, Soon Won ; An, Jae Jin ; Kim, Dae Won ; Hwang, Hyun Sook ; Lim, Soon Sung ; Kim, Duk-Soo ; Han, Kyu Hyung ; Park, Jinseu ; Eum, Won Sik ; Choi, Soo Young
Author_Institution :
Dept. of Biomed. Sci., Hallym Univ., Chunchon, South Korea
Abstract :
Though protein transduction domains (PTDs) are well known for the delivery of exogenous therapeutic proteins into cells, the low efficiency of transduction is a serious obstacle to protein transduction by PTD. Catalase (CAT) is one of the major antioxidant enzymes which cells counteract the deleterious effects of Reactive oxygen species (ROS). Among the various materials tested, we found that imipramine is an efficient Tat-catalase protein transduction enhancer into neuronal cells and more protective effects against oxidative stress. In addition, ischemic animal models, combined imipramine with Tat-catalase markedly prevented neuronal cell death in the CA1 region of the hippocampus compared Tat-catalase. Although the mechanism is not fully understood, enhancement of transduction efficiency provides a strategy for therapeutic proteins for a variety of disorders related to ROS.
Keywords :
cellular biophysics; enzymes; molecular biophysics; neurophysiology; PTD; Tat-catalase protein; antioxidant enzymes; exogenous therapeutic protein delivery; hippocampus CA1 region; imipramine; ischemic animal models; neuronal cell damage attenuation; protein transduction domains; reactive oxygen species; transduction efficiency ehancement; Antioxidant; Cell viability; Ischemia; Protein transduction; ROS; Tat-catalase;
Conference_Titel :
Bioinformatics and Biomedicine Workshops (BIBMW), 2010 IEEE International Conference on
Conference_Location :
Hong, Kong
Print_ISBN :
978-1-4244-8303-7
Electronic_ISBN :
978-1-4244-8304-4
DOI :
10.1109/BIBMW.2010.5703917