Identification and characterization of a novel cell-penetrating peptide of 30Kc19 protein derived from Bombyx mori |
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Affiliation: | 1. The School of Chemical and Biological Engineering, Seoul National University, Seoul 151-744, Republic of Korea;2. Interdisciplinary Program for Bioengineering, Seoul National University, Seoul 151-744, Republic of Korea;3. Division of Bioengineering, Incheon National University, Incheon 406-772, Republic of Korea;4. Advanced Institutes of Convergence Technology, Suwon 443-270, Republic of Korea;1. State Key Laboratory of Silkworm Genome Biology, Southwest University, Chongqing 400716, China;2. Key Laboratory for Sericulture Functional Genomics and Biotechnology of Agricultural Ministry, Southwest University, Chongqing 400716, China;1. Beckman Institute for Advanced Science and Technology, Center for Biophysics and Quantitative Biology, University of Illinois at Urbana-Champaign, Champaign, Illinois;2. Department of Physics and Department of Chemistry, University of Illinois at Urbana-Champaign, Champaign, Illinois;3. Centre for Biodiscovery and Molecular Development of Therapeutics, Australian Institute of Tropical Health and Medicine, James Cook University, Cairns, Queensland, Australia;1. Departament de Fisiologia – Facultat de Farmàcia, Universitat de Barcelona, Avda. Joan XXIII s/n, 08028 Barcelona, Spain;3. Departament de Fisicoquímica – Facultat de Farmàcia, Universitat de Barcelona, Avda. Joan XXIII s/n, 08028 Barcelona, Spain |
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Abstract: | Cell-penetrating peptides (CPPs) or protein transduction domains (PTDs) have attracted increasing attention due to their high potential to deliver various, otherwise impermeable, bioactive agents, such as drugs and proteins across cell membranes. A number of CPPs have been discovered since then. Recently, 30Kc19 protein has attracted attention because it was the first cell-penetrating protein that has been found in insect hemolymph. Here, we report a cell-penetrating peptide derived from 30Kc19 protein, VVNKLIRNNKMNC, which efficiently penetrates cells when supplemented to medium for mammalian cell culture. Moreover, like other CPPs, this “Pep-c19” also efficiently delivered cell-impermeable cargo proteins, such as green fluorescent protein (GFP) into cells. In addition to the in vitro system, Pep-c19 exhibited the cell-penetrating property in vivo. When Pep-c19 was intraperitoneally injected into mice, Pep-c19 successfully delivered cargo proteins into various organ tissues with higher efficiency than the 30Kc19 protein itself, and without toxicity. Our data demonstrates that Pep-c19 has a great potential as a cell-penetrating peptide that can be used as a therapeutic tool to efficiently deliver different cell-impermeable cargo molecules into the tissues of various organs. |
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Keywords: | 30Kc19 protein Cell-penetrating peptide (CPP) Protein delivery |
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