Engineered protein nanoparticles for invivo tumor detection

Keum Young Ahn, Ho Kyung Ko, Bo Ram Lee, Eun Jung Lee, Jong Hwan Lee, Youngro Byun, Ick Chan Kwon, Kwang Meyung Kim, Jeewon Lee

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Two different protein nanoparticles that are totally different in shape and surface structure, i.e. Escherichia coli DNA-binding protein (eDPS) (spherical, 10nm) and Thermoplasma acidophilum proteasome (tPTS) (cylindrical, 12×15nm) were engineered for invivo optical tumor detection: arginine-glycine-aspartic acid (RGD) peptide (CDCRGDCFC) was genetically inserted to the surface of each protein nanoparticle, and also near-infrared fluorescence dye was chemically linked to the surface lysine residues. The specific affinity of RGD for integrin (αvβ3) facilitated the uptake of RGD-presenting protein nanoparticles by integrin-expressing tumor cells, and also the protein nanoparticles neither adversely affected cell viability nor induced cell damage. After intravenously injected to tumor-bearing mice, all the protein nanoparticles successfully reached tumor with negligible renal clearance, and then the surface RGD peptides caused more prolonged retention of protein nanoparticles in tumor and accordingly higher fluorescence intensity of tumor image. In particular, the fluorescence of tumor image was more intensive with tPTS than eDPS, which is due presumably to longer invivo half-life and circulation of tPTS that originates from thermophilic and acidophilic bacterium. Although eDPS and tPTS were used as proof-of-concept in this study, it seems that other protein nanoparticles with different size, shape, and surface structure can be applied to effective invivo tumor detection.

Original languageEnglish
Pages (from-to)6422-6429
Number of pages8
JournalBiomaterials
Volume35
Issue number24
DOIs
Publication statusPublished - 2014 Jan 1

Fingerprint

Nanoparticles
Tumors
Proteins
Proteasome Endopeptidase Complex
Neoplasms
Fluorescence
Cells
Integrins
Surface structure
Peptides
Bearings (structural)
Arginine
Escherichia coli Proteins
DNA-Binding Proteins
Aspartic Acid
Glycine
Escherichia coli
Lysine
Half-Life
Amino acids

ASJC Scopus subject areas

  • Biomaterials
  • Bioengineering
  • Ceramics and Composites
  • Mechanics of Materials
  • Biophysics

Cite this

Ahn, K. Y., Ko, H. K., Lee, B. R., Lee, E. J., Lee, J. H., Byun, Y., ... Lee, J. (2014). Engineered protein nanoparticles for invivo tumor detection. Biomaterials, 35(24), 6422-6429. https://doi.org/10.1016/j.biomaterials.2014.04.041

Engineered protein nanoparticles for invivo tumor detection. / Ahn, Keum Young; Ko, Ho Kyung; Lee, Bo Ram; Lee, Eun Jung; Lee, Jong Hwan; Byun, Youngro; Kwon, Ick Chan; Kim, Kwang Meyung; Lee, Jeewon.

In: Biomaterials, Vol. 35, No. 24, 01.01.2014, p. 6422-6429.

Research output: Contribution to journalArticle

Ahn, KY, Ko, HK, Lee, BR, Lee, EJ, Lee, JH, Byun, Y, Kwon, IC, Kim, KM & Lee, J 2014, 'Engineered protein nanoparticles for invivo tumor detection', Biomaterials, vol. 35, no. 24, pp. 6422-6429. https://doi.org/10.1016/j.biomaterials.2014.04.041
Ahn KY, Ko HK, Lee BR, Lee EJ, Lee JH, Byun Y et al. Engineered protein nanoparticles for invivo tumor detection. Biomaterials. 2014 Jan 1;35(24):6422-6429. https://doi.org/10.1016/j.biomaterials.2014.04.041
Ahn, Keum Young ; Ko, Ho Kyung ; Lee, Bo Ram ; Lee, Eun Jung ; Lee, Jong Hwan ; Byun, Youngro ; Kwon, Ick Chan ; Kim, Kwang Meyung ; Lee, Jeewon. / Engineered protein nanoparticles for invivo tumor detection. In: Biomaterials. 2014 ; Vol. 35, No. 24. pp. 6422-6429.
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