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Title: Arginine-rich intracellular delivery peptides noncovalently transport protein into living cells

Journal Article · · Biochemical and Biophysical Research Communications
 [1];  [1];  [2];  [1];  [1];  [2];  [2];  [1];  [1]
  1. Department of Life Science, National Dong Hwa University, Hualien 97401, Taiwan (China)
  2. Institute of Pharmacology and Toxicology, Tzu Chi University, Hualien 97004, Taiwan (China)

Plasma membranes of plant or animal cells are generally impermeable to peptides or proteins. Many basic peptides have previously been investigated and covalently cross-linked with cargoes for cellular internalization. In the current study, we demonstrate that arginine-rich intracellular delivery (AID) peptides are able to deliver fluorescent proteins or {beta}-galactosidase enzyme into animal and plant cells, as well as animal tissue. Cellular internalization and transdermal delivery of protein could be mediated by effective and nontoxic AID peptides in a neither fusion protein nor conjugation fashion. Therefore, noncovalent AID peptides may provide a useful strategy to have active proteins function in living cells and tissues in vivo.

OSTI ID:
20854388
Journal Information:
Biochemical and Biophysical Research Communications, Vol. 346, Issue 3; Other Information: DOI: 10.1016/j.bbrc.2006.05.205; PII: S0006-291X(06)01238-1; Copyright (c) 2006 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0006-291X
Country of Publication:
United States
Language:
English