Woo‐Jae Chung
성균관대학교 의과대학 생화학과 · 생화학·유전·분자생물학
우재청 교수의 연구실은 생체모방적 나노소재 및 생체재료를 중심으로, 나노입자, 바이러스 유도 구조체, 고분자 복합체를 활용한 조직공학 및 단백질 정제 기술을 개발하고 있습니다. 특히 M13 박테리오파지 기반의 정렬된 나노섬유 구조를 통해 세포의 행동을 정밀하게 유도하는 생체적합성 재료를 설계하며, 자기성 나노입자나 실리카 코팅을 통한 기능화도 진행하고 있습니다. 이는 뼈, 신경 등 다양한 조직 재생 응용에 기여할 수 있는 첨단 생체재료의 설계 원리를 확립하는 데 초점이 맞춰져 있습니다.
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
This paper presents a facile method for preparation of silica coated monodisperse superparamagnetic microsphere. Herein, monodisperse porous polystyrene-divinylbenzene microbeads were prepared by seeded emulsion polymerization and subsequently sulfonated with acetic acid/H 2 SO 4 . The as-prepared sulfonated macroporous beads were magnetized in presence of Fe 2+ /Fe 3+ under alkaline condition and were subjected to silica coating by sol-gel process, providing water compatibility, easily modifiab
The biogenesis of inorganic/organic composite materials such as bone typically involves the process of templated mineralization. Biomimetic synthesis of bone-like materials therefore requires the development of organic scaffolds that mediate mineralization of hydroxyapatite (HAP), the major inorganic component of bone. Using phage display, we identified a 12-residue peptide that bound to single-crystal HAP and templated the nucleation and growth of crystalline HAP mineral in a sequence- and comp
Designing biomimetic matrices with precisely controlled structural organization that provides biochemical and physical cues to regulate cell behavior is critical for the development of tissue-regenerating materials. We have developed novel liquid-crystalline film matrices made from genetically engineered M13 bacteriophages (viruses) that exhibit the ability to control and guide cell behavior for tissue-regenerating applications. To facilitate adhesion between the viruses and cells, 2700 copies o
We report on a novel method to utilize genetically engineered M13 phages as functional nano building blocks that can form structurally aligned film and fiber matrices for tissue engineering scaffolds. Two- and three-dimensional directionally aligned long range ordered structures were constructed using shearing and polyionic complexation with cationic polymers. Further we have demonstrated that aligned phage-based tissue engineering materials can guide and stimulate the growth of the target fibro
A bead affinity chromatography system, which was based on the photolytic elution method, was integrated into a glass-silicon microchip to purify specific target proteins. CutiCore beads, which were coupled with a photo-cleavable ligand, such as biotin and an RNA aptamer, were introduced into a filter chamber in the microchip. The protein mixture containing target protein labeled with fluorescein isothiocyanate (FITC) was then passed through the packed affinity beads in the microchamber by pressu
As the M13 bacteriophage, which has integrin binding and calcium binding sites, provides topological cues from the nanofibrous shape and biochemical cues from the Arg-Gly-Asp (RGD) sequence attached to the surface of fibrous phage, it has been recommended as a bioactive component for use in bone tissue engineering. However, although it has good biological activities, its low mechanical properties and low processing ability represent major issues that must be overcome before its use as a tissue e
A hybrid scaffold (M13-phage/alginate and PCL) was proposed as a biomedical scaffold.