Intracellular protein delivery activity of peptides derived from insulin-like growth factor binding proteins 3 and 5.

Abstract:

:Insulin-like growth factor binding proteins (IGFBPs) have various IGF-independent cellular activities, including receptor-independent cellular uptake followed by transcriptional regulation, although mechanisms of cellular entry remain unclear. Herein, we focused on their receptor-independent cellular entry mechanism in terms of protein transduction domain (PTD) activity, which is an emerging technique useful for clinical applications. The peptides of 18 amino acid residues derived from IGFBP-3 and IGFBP-5, which involve heparin-binding regions, mediated cellular delivery of an exogenous protein into NIH3T3 and HeLa cells. Relative protein delivery activities of IGFBP-3/5-derived peptides were approximately 20-150% compared to that of the HIV-Tat peptide, a potent PTD. Heparin inhibited the uptake of the fusion proteins with IGFBP-3 and IGFBP-5, indicating that the delivery pathway is heparin-dependent endocytosis, similar to that of HIV-Tat. The delivery of GST fused to HIV-Tat was competed by either IGFBP-3 or IGFBP-5-derived synthetic peptides. Therefore, the entry pathways of the three PTDs are shared. Our data has shown a new approach for designing protein delivery systems using IGFBP-3/5 derived peptides based on the molecular mechanisms of IGF-independent activities of IGFBPs.

journal_name

Exp Cell Res

authors

Goda N,Tenno T,Inomata K,Shirakawa M,Tanaka T,Hiroaki H

doi

10.1016/j.yexcr.2008.05.008

subject

Has Abstract

pub_date

2008-08-01 00:00:00

pages

2352-61

issue

13

eissn

0014-4827

issn

1090-2422

pii

S0014-4827(08)00210-3

journal_volume

314

pub_type

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