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      https://www.riss.kr/link?id=A105449509

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      부가정보

      다국어 초록 (Multilingual Abstract)

      Multiple sclerosis is a chronic disorder commonly occurred in the central nervous system and is an autoimmune disease. Corticosteroids are used as a short-term treatment for multiple sclerosis, but they cause side effects. Therefore, interferon beta h...

      Multiple sclerosis is a chronic disorder commonly occurred in the central nervous system and is an autoimmune disease. Corticosteroids are used as a short-term treatment for multiple sclerosis, but they cause side effects. Therefore, interferon beta having antiviral and anti-inflammatory effects, is used for long-term treatment. Interferon beta-1a, produced in Chinese hamster ovary cells, is glycosylated upon biosynthesis and forms glycoform, which is similar to naturally occurring protein. However, its process has disadvantages such as slow cell growth, low yield and high contamination possibility. Also, recombinant Escherichia coli is widely used for the production of interferon beta-1b due to its rapid growth and easy process scale up, but it lacks post-translational modification, leading to low activity. In addition, the produced Interferon beta-1b might cause protein aggregation due to misfolding. Alternatively, yeast can be used as a production host possessing N-glycosylation activity. Therefore, the choice of expression system in the production of interferon beta should be carefully selected in relation to the quality and yield.

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      목차 (Table of Contents)

      • Abstract
      • 1. INTRODUCTION
      • 2. 본론
      • 3. CONCLUSION
      • REFERENCES
      • Abstract
      • 1. INTRODUCTION
      • 2. 본론
      • 3. CONCLUSION
      • REFERENCES
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      참고문헌 (Reference)

      1 Rice, G., "Treatment with interferon beta-1b improves quality of life in multiple sclerosis" 26 : 276-282, 1999

      2 Harde, D. R., "The use of zwittergent 3-14 in the purification of recombinant human interferon-${\beta}$ ser17 (Betaseron)" 15 : 31-37, 1995

      3 Singh, V., "The paradigm of Th1 and Th2 cytokines" 20 : 147-161, 1999

      4 Beck, R. W., "The effect of corticosteroids for acute optic neuritis on the subsequent development of multiple sclerosis" 329 : 1764-1769, 1993

      5 Kieseier, B. C, "The Mechanism of action of interferon-${\beta}$ in relapsing multiple sclerosis" 25 : 491-502, 2011

      6 Mattanovich, D., "Stress in recombinant protein producing yeasts" 113 : 121-135, 2004

      7 Mattanovich, D., "Recombinant Gene Expression. Methods in Molecular Biology (Methods and Protocols)" Humana Press 329-358, 2012

      8 Sahdev, S., "Production of active eukaryotic proteins through bacterial expression systems: A review of the existing biotechnology strategies" 307 : 249-264, 2008

      9 Spearman, M., "Production and glycosylation of recobinant ${\beta}$-interferon in suspension and cytopore microcarrier cultures of CHO cells" 21 : 31-39, 2005

      10 Prisms, S, "PRISMS-4: Long-term efficacy of interferonbeta- 1a in relapsing MS" 56 : 1628-, 2001

      1 Rice, G., "Treatment with interferon beta-1b improves quality of life in multiple sclerosis" 26 : 276-282, 1999

      2 Harde, D. R., "The use of zwittergent 3-14 in the purification of recombinant human interferon-${\beta}$ ser17 (Betaseron)" 15 : 31-37, 1995

      3 Singh, V., "The paradigm of Th1 and Th2 cytokines" 20 : 147-161, 1999

      4 Beck, R. W., "The effect of corticosteroids for acute optic neuritis on the subsequent development of multiple sclerosis" 329 : 1764-1769, 1993

      5 Kieseier, B. C, "The Mechanism of action of interferon-${\beta}$ in relapsing multiple sclerosis" 25 : 491-502, 2011

      6 Mattanovich, D., "Stress in recombinant protein producing yeasts" 113 : 121-135, 2004

      7 Mattanovich, D., "Recombinant Gene Expression. Methods in Molecular Biology (Methods and Protocols)" Humana Press 329-358, 2012

      8 Sahdev, S., "Production of active eukaryotic proteins through bacterial expression systems: A review of the existing biotechnology strategies" 307 : 249-264, 2008

      9 Spearman, M., "Production and glycosylation of recobinant ${\beta}$-interferon in suspension and cytopore microcarrier cultures of CHO cells" 21 : 31-39, 2005

      10 Prisms, S, "PRISMS-4: Long-term efficacy of interferonbeta- 1a in relapsing MS" 56 : 1628-, 2001

      11 Ashnagar, F., "Optimizing primary recovery and refolding of human interferon-b from Escherichia coli inclusion bodies" 12 : 26-34, 2014

      12 Soldan, S. S., "Neuroimmune Pharmacol" Springer 239-255, 2008

      13 Cree, B. A. C, "Multiple sclerosis genetics" 122 : 193-209, 2014

      14 Goldenberg, M. M, "Multiple Sclerosis Review" 37 : 175-184, 2012

      15 Arnold, S., "Method for the purification of interferon-B. US Patent, 424/85.6; 530/351"

      16 Sandig, V., "Mammalian cells: Production of recombinant proteins: Novel microbial and eukaryotic expression systems" Wiley-VCH Weinheim 233-252, 2005

      17 Simon, J. H., "Magnetic resonance studies of intramuscular interferon ${\beta}$-1a for relapsing multiple sclerosis" 43 : 79-87, 1998

      18 Li, D. K., "Magnetic resonance imaging results of the PRISMS trial: A randomized, double-blind, placebo-controlled study of interferon-${\beta}$ 1 a in relapsing-remitting multiple sclerosis" 46 : 197-206, 1999

      19 Goffeau, A., "Life with 6000 genes" 274 : 546-567, 1996

      20 Romanov, V. P., "Isolation of human interferon ${\beta}1b$ (Ser17) expressed in E. coli with the use of ion-exchange chromatography" 37 : 292-297, 2011

      21 Dhib-Jalbut S., "Interferon-${\beta}$ mechanisms of action in multiple sclerosis" 74 : S17-S24, 2010

      22 Paty, D., "Interferon beta?1b is effective in relapsing-remitting multiple sclerosis II. MRI analysis results of a multicenter, randomized, double?blind, placebo?controlled trial" 43 : 662-662, 1993

      23 McCormick, F. R. A. N. K., "Inducible expression of amplified human beta interferon genes in CHO cells" 4 : 166-172, 1984

      24 Mastrangeli, R., "In vitro biological characterization of IFN-${\beta}$-1a major glycoforms" 25 : 21-29, 2014

      25 Zago, P., "Improving human interferon-${\beta}$ production in mammalian cell lines by insertion of an intronic sequence within its naturally uninterrupted gene" 52 : 191-198, 2009

      26 Villela Dr. A., "Human interferon Β1ser17: Coding DNA synthesis, expression, purification and characterization of bioactive recombinant protein" 2 : 1948-5948, 2010

      27 Song, K., "Glycoengineering of interferon-${\beta}$ 1a improves its biophysical and pharmacokinetic properties" 9 : e96967-, 2014

      28 Feizi, A., "Genome-scale modeling of the protein secretory machinery in yeast" 8 : e63284-, 2013

      29 Aricescu, A. R., "Expression of recombinant glycoproteins in mammalian cells: Towards an integrative approach to structural biology" 23 : 345-356, 2013

      30 Skoko, N., "Expression and characterization of human interferon-${\beta}1$ in the methylotrophic yeast Pichia pastoris" 38 : 257-265, 2003

      31 Weinshenker, B. G, "Epidemiology of multiple sclerosis" 14 : 291-308, 1996

      32 Han, Y. K., "Enhanced interferon- ${\beta}$ production by CHO cells through elevated osmolality and reduced culture temperature" 25 : 1440-1447, 2009

      33 Rodriguez, J., "Enhanced Production of Monomeric Interferon-${\beta}$ by CHO Cells through the Control of Culture Conditions" 21 : 22-30, 2005

      34 Kamionka, M., "Engineering of therapeutic proteins production in Escherichia coli" 12 : 268-274, 2011

      35 Chernajovsky, Y., "Efficient constitutive production of human fibroblast interferon by hamster cells transformed with the IFN-${\beta}1$ gene fused to an SV40 early promoter" 3 : 297-308, 1984

      36 La Mantia, L., "Double-blind trial of dexamethasone versus methylprednisolone in multiple sclerosis acute relapses" 34 : 199-203, 1994

      37 Calabresi, P. A, "Diagnosis and management of multiple sclerosis" 70 : 1935-1944, 2004

      38 Rao, D. V. K., "Cloning, high expression and purification of recombinant human Intereferon-${\beta}$-1b in Escherichia coli" 158 : 140-154, 2009

      39 Spearman, M., "Cell Technology for Cell Products" Springer 71-85, 2007

      40 Walsh, G, "Biopharmaceutical benchmarks 2014" 32 : 992-1000, 2014

      41 Mohan, C., "Assessment of cell engineering strategies for improved therapeutic protein production in CHO cells" 3 : 624-630, 2008

      42 Lai, T., "Advances in mammalian cell line development technologies for recombinant protein production" 6 : 579-603, 2013

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2022 평가예정 재인증평가 신청대상 (재인증)
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      2016-01-01 평가 등재학술지 선정 (계속평가) KCI등재
      2015-12-01 평가 등재후보로 하락 (기타) KCI등재후보
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-08-28 학술지명변경 한글명 : 한국생물공학회지 -> KSBB Journal
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      KCI등재
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      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2002-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      1999-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 0.37 0.37 0.38
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.37 0.36 0.662 0.02
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