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Lung epithelial binding peptide-linked high mobility group box-1: A box for lung epithelial cell-specific delivery of DNA

Authors
Kim, Hyun AhPark, Ji HwanCho, Su HeeLee, Minhyung
Issue Date
Aug-2011
Publisher
TAYLOR & FRANCIS LTD
Keywords
Lung epithelial cells; gene delivery; high mobility group box-1; recombinant peptide
Citation
JOURNAL OF DRUG TARGETING, v.19, no.7, pp.589 - 596
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF DRUG TARGETING
Volume
19
Number
7
Start Page
589
End Page
596
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/167884
DOI
10.3109/1061186X.2010.547584
ISSN
1061-186X
Abstract
High mobility group box-1 A box (HMGB1A) is an anti-inflammatory peptide originating from HMGB1. A previous report demonstrated that recombinant HMGB1A could deliver DNA into cells. Lung epithelial-specific gene delivery is required for the gene therapy of various lung diseases such as acute lung injury. In this study, a lung epithelial-specific DNA carrier was produced by linking the lung epithelial binding peptide (LEBP) to HMGB1A. An LEBP-linked HMGB1A (LEBP-HMGB1A) expression vector, pET21a-LEBP-HMGB1A, was constructed. LEBP-HMGB1A was expressed in BL21 strain and purified by consecutive applications of nickel affinity chromatography and cationic exchange chromatography. In a gel retardation assay, LEBP-HMGB1A completely retarded DNA at a 5:1 weight ratio (peptide: DNA). LEBP-HMGB1A/DNA complexes were prepared at various weight ratios, to which a fixed amount of polyethylenimine (2 kDa, PEI2k) was added to increase the proton buffering effect of the complex. LEBP-HMGB1A had the highest transfection efficiency to L2 lung epithelial cells at a 20: 1 weight ratio (peptide: DNA). At this ratio, LEBPHMGB1A had a higher transfection efficiency than poly-L-lysine (PLL) as well as HMGB1A without LEBP. A cytotoxicity assay showed that LEBP-HMGB1A was not toxic to L2 cells. Therefore, LEBP-HMGB1A may be useful in developing gene therapies for lung diseases.
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