» Articles » PMID: 12678854

Protein Therapy: in Vivo Protein Transduction by Polyarginine (11R) PTD and Subcellular Targeting Delivery

Overview
Specialty Biochemistry
Date 2003 Apr 8
PMID 12678854
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

Protein Therapy is a newly developed method, which allows proteins, peptides and biologically active compounds to penetrate across the plasma membrane of eukaryotic cells by a polyarginine (most efficiently by 11-arginine, 11R) protein transduction domain. This method enables us to control the localization of targeted substances in subcellular compartments, such as the nuclei, mitochondria and post-synaptic density. The method is very efficient and applicable not only to cultured cells but also to tissue slices and the whole animal. Brain, heart, skeletal muscle, liver, pancreas and lymphocytes are efficient target organs and tissues for Protein Therapy. The method is therefore a very useful strategy in the post-genomic era. In this mini-review, the development of Protein Therapy and its application for cancer cells and neuroscience study will be shown.

Citing Articles

Cellular protection from HO toxicity by Fv-Hsp70: protection via catalase and gamma-glutamyl-cysteine synthase.

Hino C, Chan G, Jordaan G, Chang S, Saunders J, Bashir M Cell Stress Chaperones. 2023; 28(4):429-439.

PMID: 37171750 PMC: 10352194. DOI: 10.1007/s12192-023-01349-6.


Molecular targeting of cell-permeable peptide inhibits pancreatic ductal adenocarcinoma cell proliferation.

Sato S, Nakamura T, Katagiri T, Tsuchikawa T, Kushibiki T, Hontani K Oncotarget. 2018; 8(69):113662-113672.

PMID: 29371937 PMC: 5768354. DOI: 10.18632/oncotarget.21939.


Regeneration of hyaline-like cartilage in situ with SOX9 stimulation of bone marrow-derived mesenchymal stem cells.

Zhang X, Wu S, Naccarato T, Prakash-Damani M, Chou Y, Chu C PLoS One. 2017; 12(6):e0180138.

PMID: 28666028 PMC: 5493350. DOI: 10.1371/journal.pone.0180138.


Protein therapy using MafA fused to a polyarginine transduction domain attenuates glucose levels of streptozotocin‑induced diabetic mice.

Lu J, Lin L, Dong H, Meng X, Fang F, Wang Q Mol Med Rep. 2017; 15(6):4041-4048.

PMID: 28487936 PMC: 5436157. DOI: 10.3892/mmr.2017.6536.


A cell-permeable gadolinium contrast agent for magnetic resonance imaging of copper in a Menkes disease model.

Que E, New E, Chang C Chem Sci. 2014; 3(6):1829-1834.

PMID: 25431649 PMC: 4243178. DOI: 10.1039/C2SC20273E.