홍종광 교수
Jong Kwang Hong
연세대학교 생명공학과 · 생화학·유전·분자생물학
연구실 소개
홍종광 교수의 연구실은 생물의약품 생산을 위한 식물 및 동물세포 발현체계의 당사슬 공학 기반 기술 개발에 주력하고 있습니다. 특히 레이시 셀을 활용한 고순도 망간형 당단쇄(Man7/8/9) 생성 전략과 중국선충우세포(CHO)에서의 NAD+ 대사 조절을 통한 대사 경로 최적화를 통해 바이오의약품의 생산성과 품질을 향상시키는 데 초점을 맞추고 있습니다. 또한 노화 관련 근육량 감소(사르코페니아) 예방을 위한 후생물질(postbiotic) 및 천연물 복합제제의 기능성 평가도 함께 진행하고 있습니다.
연구 현황
연구 성과 추이
표시된 성과는 수집된 데이터 기준으로 산출되며, 일부 차이가 있을 수 있습니다.
주요 논문
15Abstract Glycoengineering of plant expression systems is a prerequisite for the production of biopharmaceuticals that are compatible with animal-derived glycoproteins. Large amounts of high-mannose glycans such as Man 7 GlcNAc 2 , Man 8 GlcNAc 2 , and Man 9 GlcNAc 2 (Man7/8/9), which can be favorably modified by chemical conjugation of mannose-6-phosphate, are desirable for lysosomal enzyme targeting. This study proposed a rice cell-based glycoengineering strategy using two different mannosidase
Abstract In the previous study, the culture medium was treated with nicotinamide adenine dinucleotide (NAD + ) under the hypothesis that NAD + regeneration is a major factor causing excessive lactate accumulation in Chinese hamster ovary (CHO) cells. The NAD + treatment improved metabolism by not only reducing the Warburg effect but also enhancing oxidative phosphorylation, leading to enhanced antibody production. Building on this, four NAD + precursors – nicotinamide mononucleotide (NMN), nicot
Background/Objectives: Sarcopenia is an age-related disease resulting in muscle mass deterioration and declining strength and functional ability. Muscle protein degradation pathways are activated through the ubiquitin–proteasome system, which is integral to the pathogenesis of sarcopenia. This study examined the capability of Lactobacillus plantarum beLP1 as a postbiotic ingredient of kimchi that prevents sarcopenia. Methods: We evaluated cell viability and measured diameters in a C2C12 myotube
Abstract Aerobic glycolysis and its by‐product lactate accumulation are usually associated with adverse culture phenotypes such as poor cell viability and productivity. Due to the lack of knowledge on underlying mechanisms and accompanying biological processes, the regulation of aerobic glycolysis has been an ongoing challenge in culture process development for therapeutic protein productivity. Nicotinamide adenine dinucleotide (NAD + ), a coenzyme and co‐substrate in energy metabolism, promotes
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