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Phage Assembly Using APTES-Conjugation of Major Coat p8 Protein for Possible Scaffolds
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  • Phage Assembly Using APTES-Conjugation of Major Coat p8 Protein for Possible Scaffolds
  • Phage Assembly Using APTES-Conjugation of Major Coat p8 Protein for Possible Scaffolds
저자명
Kim. Young Jun,Korkmaz. Nuriye,Nam. Chang Hoon
간행물명
Interdisciplinary Bio Central
권/호정보
2012년|4권 3호|pp.9-10 (2 pages)
발행정보
한국생물정보시스템생물학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

Filamentous phages have been in the limelight as a new type of nanomaterial. In this study, genetically and chemically modified fd phage was used to generate a biomimetic phage self-assembly product. Positively charged fd phage (p8-SSG) was engineered by conjugating 3-aminopropyltriethoxysilane (APTES) to hydroxyl groups of two serine amino acid residues introduced at the N-terminus of major coat protein, p8. In particular, formation of a phage network was controlled by changing mixed ratios between wild type fd phage and APTES conjugated fd-SSG phage. Assembled phages showed unique bundle and network like structures. The bacteriophage based self-assembly approach illustrated in this study might contribute to the design of three dimensional microporous structures. In this work, we demonstrated that the positively charged APTES conjugated fd-SSG phages can assemble into microstructures when they are exposed to negatively charged wild-type fd phages through electrostatic interaction. In summary, since we can control the phage self-assembly process in order to obtain bundle or network like structures and since they can be functionalized by means of chemical or genetic modifications, bacteriophages are good candidates for use as bio-compatible scaffolds. Such new type of phage-based artificial 3D architectures can be applied in tuning of cellular structures and functions for tissue engineering studies.