• 제목/요약/키워드: shock proteins

검색결과 372건 처리시간 0.024초

CspA의 발현이 저온에서의 재조합 단백질 생산성에 미치는 영향에 관한 연구 (A study on the effect of CspA expression on the productivity of recombinant protein at low temperature)

  • 김수현;허미애;이선구
    • KSBB Journal
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    • 제24권1호
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    • pp.96-100
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    • 2009
  • 본 연구에서는 저온에서의 재조합 단백질 생산성 향상을 위하여 저온에서 RNA 샤페론 활성을 지닌다고 알려진 CspA 단백질의 발현이 서로 다른 온도에서 대장균의 성장 및 GFP의 발현 속도에 어떻게 영향을 미치는지를 살펴보았다. $20^{\circ}C$, $25^{\circ}C$, $37^{\circ}C$에서는 세포 성장 및 GFP의 생산이 CspA의 발현에 영향을 받지 않았으나, $15^{\circ}C$에서는 GFP의 총 생산성이 CspA의 동시 발현에 의해 향상되었으며 이는 세포 성장 속도의 향상에 기인함을 확인하였다. 결론적으로 CspA의 발현은 $15^{\circ}C$에서 세포 당 재조합 단백질 생산량의 증가에는 영향을 미치지 않으나, 즉 재조합 단백질의 번역 효율에는 큰 영향을 미치지 않으나, 대장균 성장 속도에 영향을 미치며, 이를 통해 재조합 단백질의 총 생산량 향상을 유도 할 수 있을 것으로 기대된다.

녹차 카테킨 EGCG의 노출에 따른 식중독 세균인 용혈성 Aeromonas sp. MH-8의 특성조사 (Characterization of Hemolytic Aeromonas sp. MH-8 Responding to the Exposure of Green Tea Catechin, EGCG)

  • 김동민;오계헌
    • KSBB Journal
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    • 제31권4호
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    • pp.228-236
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    • 2016
  • The aim of this study was to characterize the hemolytic Aeromonas sp. MH-8 exposed to green tea catechin, epigallocatechin gallate (EGCG). Initially, the hemolytic Aeromonas sp. MH-8 was enriched and isolated from stale fish. Bactericidal effects of MH-8 exposed to EGCG ranging from 1 mg/mL to 4 mg/mL were monitored, and complete bactericidal effects were achieved within 3 h at 3 mg/mL and higher concentrations. SDS-PAGE with silver staining revealed that the amount of lipopolysaccharides increased or decreased in the strain MH-8 treated to different concentrations and exposing periods of EGCG in exponentially growing cultures. The stress shock proteins (70-kDa DnaK and 60-kDa GroEL), which might contribute to enhancing the cellular resistance to the cytotoxic effect of EGCG, were induced at different concentrations of EGCG exposed to cell culture of MH-8. Scanning electron microscopic analysis demonstrated the presence of irregular rod shapes with umbilicated surfaces for cells treated with EGCG. 2-DE of soluble protein fractions from MH-8 cultures showed 18 protein spots changed by EGCG exposure. These proteins involved in chaperons (e.g., DnaK, GroEL and trigger factor), enterotoxins (e.g., aerolysin and phospholipase C precursor), LPS synthesis (e.g., LPS biosynthesis protein and outer membrane protein A precursor), and various biosynthesis and energy metabolism were identified by peptide mass fingerprinting using MALDI-TOF. In consequence, EGCG was found to have substantial antibacterial effects against food-poisoning causing bacterium, hemolytic Aeromonas sp. MH-8. Also the results provide clues for understanding the mechanism of EGCG-induced stress and cytotoxicity on Aeromonas sp. MH-8.

Nitric Oxide as a Pro-apoptotic as well as Anti-apoptotic Modulator

  • Choi, Byung-Min;Pae, Hyun-Ock;Jang, Seon-Il;Kim, Young-Myeong;Chung, Hun-Taeg
    • BMB Reports
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    • 제35권1호
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    • pp.116-126
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    • 2002
  • Nitric oxide (NO), synthesized from L-arginine by NO synthases, is a small, lipophilic, diffusible, highly reactive molecule with dichotomous regulatory roles in many biological events under physiological and pathological conditions. NO can promote apoptosis (pro-apoptosis) in some cells, whereas it inhibits apoptosis (anti-apoptosis) in other cells. This complexity is a consequence of the rate of NO production and the interaction with biological molecules such as metal ion, thiol, protein tyrosine, and reactive oxygen species. Long-lasting overproduction of NO acts as a pro-apoptotic modulator, activating caspase family proteases through the release of mitochondrial cytochrome c into cytosol, up-regulation of the p53 expression, and alterations in the expression of apoptosis-associated proteins, including the Bcl-2 family. However, low or physiological concentrations of NO prevent cells from apoptosis that is induced by the trophic factor withdrawal, Fas, $TNF{\alpha}$/ActD, and LPS. The anti-apoptotic mechanism is understood on the basis of gene transcription of protective proteins. These include: heat shock protein, hemeoxygenase, or cyclooxygenase-2 and direct inhibition of the apoptotic executive effectors caspase family protease by S-nitrosylation of the cysteine thiol group in their catalytic site in a cell specific way. Our current understanding of the mechanisms by which NO exerts both pro- and anti-apototic action is discussed in this review article.

Transcriptome-based identification of water-deficit stress responsive genes in the tea plant, Camellia sinensis

  • Tony, Maritim;Samson, Kamunya;Charles, Mwendia;Paul, Mireji;Richard, Muoki;Mark, Wamalwa;Stomeo, Francesca;Sarah, Schaack;Martina, Kyalo;Francis, Wachira
    • Journal of Plant Biotechnology
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    • 제43권3호
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    • pp.302-310
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    • 2016
  • A study aimed at identifying putative drought responsive genes that confer tolerance to water stress deficit in tea plants was conducted in a 'rain-out shelter' using potted plants. Eighteen months old drought tolerant and susceptible tea cultivars were each separately exposed to water stress or control conditions of 18 or 34% soil moisture content, respectively, for three months. After the treatment period, leaves were harvested from each treatment for isolation of RNA and cDNA synthesis. The cDNA libraries were sequenced on Roche 454 high-throughput pyrosequencing platform to produce 232,853 reads. After quality control, the reads were assembled into 460 long transcripts (contigs). The annotated contigs showed similarity with proteins in the Arabidopsis thaliana proteome. Heat shock proteins (HSP70), superoxide dismutase (SOD), catalase (cat), peroxidase (PoX), calmodulinelike protein (Cam7) and galactinol synthase (Gols4) droughtrelated genes were shown to be regulated differently in tea plants exposed to water stress. HSP70 and SOD were highly expressed in the drought tolerant cultivar relative to the susceptible cultivar under drought conditions. The genes and pathways identified suggest efficient regulation leading to active adaptation as a basal defense response against water stress deficit by tea. The knowledge generated can be further utilized to better understand molecular mechanisms underlying stress tolerance in tea.

염증성 치은조직과 치주인대세포에서 Cytokine에 의해 유도되는 열충격단백 발현에 관한 연구 (Expression of Heat Shock Protein in Cytokine Stimulated PDL Cells and Inflamed Gingival Tissue)

  • 조인호;김덕규;김은철;유형근;신형식
    • Journal of Periodontal and Implant Science
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    • 제28권1호
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    • pp.103-120
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    • 1998
  • Prokaryotic and eukaryotic cells respond to heat stress and other environmental abuses by synthesizing a small set of stress proteins and by inhibiting post-transcription synthesis of normal proteins. The purpose of the present study was to document the stress response produced by inflamed gingival tissue in vivo, and cytokine inducted human periodontal ligament cells. Human PDL cells were exposed to TNF-$\alpha$(1ng/ml), INF-$\gamma$(200 U/ml), LPS(100ug/ml), combination of cytokine, and SDS-PAGE gels running and Western blotting analysis was done. In vivo studies, the healthy gingival tissusse of a control group and inflamed gingival tissue of adult periodontitis were studied by immunohistochemistry and histology. The results were as follows 1. HSP 47 was distributed on basal layer in healthy gingiva, but stronger stained in basal, suprabasal, and spinous layer of inflamed gingiva. 2. HSP 47 was rare on endothelial cells and mononuclear cells in healthy gingiva, but stronger expressed in inflamed gingiva. 3. HSP 70 expression was rare on epihelium and inflammatory cells hi both healthy & inflamed gingiva. 4. HSP 70 was actively expressed on endothelial cells and inflammatory cells of capillary lumen in moderately & mild inflamend gingiva. 5. PDL cells showed low level of HSP 47 protein expression which was significantly induced by cytokine stimulation (LSP only and combination). 6. Maximum HSP 70 protein induction was seen with stimulation by a combination of the cytokine, Combination of TNF-$\alpha$, INF-$\gamma$, LPS have been shown to synergistically effects of HSP 70 expression. On the above findings, HSP Is influenced by cytokine and chronic inflammation in vivo, and may be involved in protection of tissue during periodontal inflammatiom.

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Proteomic Analysis of Differentially Expressed Proteins in Bovine Endometrium with Endometritis

  • Choe, Chang-Yong;Park, Jeong-Won;Kim, Eun-Suk;Lee, Sung-Gyu;Park, Sun-Young;Lee, Jeong-Soon;Cho, Myung-Je;Kang, Kee-Ryeon;Han, Jae-Hee;Kang, Da-Won
    • The Korean Journal of Physiology and Pharmacology
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    • 제14권4호
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    • pp.205-212
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    • 2010
  • Endometritis is one of the primary reasons for reproductive failure. In order to investigate endometritis-associated marker proteins, proteomic analysis was performed on bovine endometrium with endometritis. In bovine endometritis, desmin, $\alpha$-actin-2, heat-shock protein (HSP) 27, peroxiredoxin-6, luteinizing hormone receptor isoform 1, collectin-43 precursor, deoxyribonuclease-I (DNase-I), and MHC class I heavy chain (MHC-Ih) were up-regulated. In contrast, transferrin, interleukin-2 precursor, hemoglobin $\beta$ subunit, and potassium channel tetramerisation domaincontaining 11 (KCTD11) were down-regulated in comparison to normal endometrium. The proteomic results were validated by semiquantitative-PCR and immunoblot analysis. The mRNA levels of desmin, transferrin, $\alpha$-actin-2, HSP27, KCTD11, and MHC-Ih were up-regulated by over 1.5-fold, and showed a pattern similar to their proteomic profiles. Desmin and $\alpha$-actin-2 protein showed positive correlations between proteomic analysis and immunoblot analysis. These results suggest that desmin and $\alpha$-actin-2 may play important roles in endometritis-related function, and could be useful markers for the diagnosis of bovine endometritis.

황련 열수추출물을 처치한 인간 대장암 세포 SNU-81에서의 단백질 발현 변화 (Monitoring the Change of Protein Expression in Human Colon Cancer Cell SNU-81 treated with the Water-Extract of Coptis japonica)

  • 유태모;김병수;유병철;유화승
    • 대한약침학회지
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    • 제12권1호
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    • pp.5-12
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    • 2009
  • Background : Anticancer effects of herbal medicine have been reported in various types of cancer, but the systematic approaches to explain molecular mechanism(s) are not established yet. Objective : To find the anticancer-effect and mechanism(s) of Water Extract of Coptis japonica (WECJ) colon cancer cell (SNU-81). Methods : We first selected 11 herbals, and anti-cancer effects of water-extracts from those herbals have been tested in human colon cancer cell line, SNU-81. Among the tested herbals, the WECJ significantly reduced proliferation of SNU-81. To establish a basis of understanding for anti-cancer mechanism, whole proteins have been obtained from SNU-81 harvested at 48 and 96 hrs after the treatment of WECJ, protein expression has been profiled by 2DE-based proteomic approach. Results : Various changes of the protein expression have been monitored, and most frequent dysregulation was found in the molecular chaperons including heat shock protein 90-alpha (Hsp90-alpha), 14-3-3 protein epsilon, T-complex protein 1 subunit alpha, protein disulfide-isomerase A3, and calreticulin. Interestingly, proliferation-associated protein 2G4 has been up-regulated, and it suggests the possible effect of Coptis japonica on ErbB3-regulated signal transduction pathway and growth control of human colon cancer cells. Conclusion : Based upon the present findings, the further study will focus on monitoring various cancer survival factors after artificial regulation of the proteins identified, and it would be the basis for the understanding of the Coptis japonica anti-cancer effect(s) at the molecular level.

Structural resemblance of the DNAJA-family protein, Tid1, to the DNAJB-family Hsp40

  • Jang, Jinhwa;Lee, Sung-Hee;Kang, Dong-Hoon;Sim, Dae-Won;Ryu, Kyung-Suk;Jo, Ku-Sung;Lee, Jinhyuk;Ryu, Hyojung;Kim, Eun-Hee;Won, Hyung-Sik;Kim, Ji-Hun
    • BMB Reports
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    • 제55권10호
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    • pp.488-493
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    • 2022
  • The specific pair of heat shock protein 70 (Hsp70) and Hsp40 constitutes an essential molecular chaperone system involved in numerous cellular processes, including the proper folding/refolding and transport of proteins. Hsp40 family members are characterized by the presence of a conserved J-domain (JD) that functions as a co-chaperone of Hsp70. Tumorous imaginal disc 1 (Tid1) is a tumor suppressor protein belonging to the DNAJA3 subfamily of Hsp40 and functions as a co-chaperone of the mitochondrial Hsp70, mortalin. In this work, we performed nuclear magnetic resonance spectroscopy to determine the solution structure of JD and its interaction with the glycine/phenylalanine-rich region (GF-motif) of human Tid1. Notably, Tid1-JD, whose conformation was consistent with that of the DNAJB1 JD, appeared to stably interact with its subsequent GF-motif region. Collectively with our sequence analysis, the present results demonstrate that the functional and regulatory mode of Tid1 resembles that of the DNAJB1 subfamily members rather than DNAJA1 or DNAJA2 subfamily proteins. Therefore, it is suggested that an allosteric interaction between mortalin and Tid1 is involved in the mitochondrial Hsp70/Hsp40 chaperone system.

잎들깨 수량과 단백질체 발현에 미치는 UV-B의 영향 (Effect of Elevated Ultraviolet-B Radiation on Yield and Differential Expression of Proteome in Perilla (perilla frutescens L.))

  • 홍성창;황선웅;장안철;신평균;장병춘;이철원
    • 한국환경농학회지
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    • 제25권1호
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    • pp.7-13
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    • 2006
  • 비닐하우스는 노지보다 UV-B 선량이 적고 외기와 차단되어 노지와 다른 생육환경 하에서 작물이 생육하게 된다. 본 연구는 UV-B 저선량 상태인 비닐하우스 재배 잎들깨에 UV-B를 처리하여 수량과 생리변화를 검토하고자 수행하였다. UV-B는 형광램프를 이용하여 잎들깨 수관으로부터 150, 120, 90 cm에서 처리하여 각각 노지자연량, 노지자연량+50% 증가량, 노지자연량+100% 증가량을 다른 광의 간섭이 없는 밤 9시부터 2시간씩 30일간 처리하였다. UV-B 처리에 의한 잎들깨 수량은 비닐하우스, 노지 자연량 150% 증가량, 노지자연량, 노지자연량+100% 증가량 처리 순이었다. 7월 20일의 자연 UV-B 선량은 노지 13.6 kJ/일, 비닐하우스 4.9 kJ/일로 비닐하우스의 UV-B 선량은 노지보다 64% 감소되는 것으로 측정되었다. UV-B가 균일하게 처리된 잎들깨의 단백질을 추출하여 2차원전기영동으로 분리하고, 이미지분석하여 발현량을 분석한 결과 UV-B에 의해 33개의 단백질 발현이 변화되었으며 이중 10개가 동정되었다. 동정된 단백질의 기능별로 분류하면 광합성과 관련된 것이 40%, 스트레스 및 스트레스 방어와 관련된 것이 60%였다. UV-B에 의해 발현이 감소한 단백질은 광합성과 관련된 ATP synthase CF1 alpha chain이었고 발현이 증가한 단백질은 DNA recombination and repair protein recF, Heat shock protein 21, Catalase, Galactinol synthase, S-adenosyl-L-methionine, Calcium-dependent protein kinase(CDPK)-like 로 주로 스트레스 및 스트레스 방어와 관련된 단백질들로서 UV-B는 잎들깨 세포내 DNA와 광합성기구를 손상시켜 광합성에 저해적으로 작용하여 수량을 감소시킨 것으로 판단되었다.

대두 열처리 담금 용액의 특성 (Characteristics of Soybean Soaking Water after Heat Treatment)

  • 윤혜현;전은재
    • 한국식품과학회지
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    • 제35권6호
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    • pp.1098-1103
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    • 2003
  • 열처리에 의한 대두 단백질의 용출 변화를 조사하기 위하여 만리, 태광, 은하, 풍산나물, 검정콩 1호와 일품검정의 6가지 장려품종 대두를 온도와 시간에 따라 열처리를 달리하여 침치액의 pH와 가용성 고형물함량과 단백질 특성을 살펴보았다. $60^{\circ}C$에서 90분 동안 열처리 후 침지액의 pH는 열처리 전보다 높았으며 $60^{\circ}C$에서 열처리 시간이 증가함에 따라 pH는 감소하였다. 침지액의 가용성고형물 함량은 열처리 온도에 따라서 $50^{\circ}C$ 이후 급격한 증가를 보였으며, 열처리 시간에 따라서 용출량의 증가를 보였다. 다른 대두에 비해 풍산나물과 은하의 경우 시간에 따라 비례적인 증가경향을 보였으며 검정콩 1호와 일품검정은 낮은 당도를 나타내었다. 단백질함량은 열처리 온도와 시간이 증가함에 따라 증가하였는데 검정콩1호와 일품검정은 다른 대두에 비해 각각 2배와 4배 정도 높은 단백질 농도를 나타내었다. 검정콩1호, 만리 및 은하 품종의 SDS-PAGE 특성은 모든 대두에서 비슷한 분리대를 보였다. 열처리 온도가 증가함에 따라 전체적으로 단백질 용출량이 증가하였고, $50^{\circ}C$$60^{\circ}C$에서 대략 31kDa과 16kDa의 새로운 단백질이 뚜렷하게 증가하였다. 열처리 시간이 증가함에 따라서도 단백질 용출량은 증가하였고 새로운 단백질 분획은 다른 단백질 보다 용출량이 더 증가하였다. 선행연구와의 비교로 열처리에 의해 나타난 31kDa와 16kDa의 단백질은 장려품종 대두에서 합성된 열충격 단백질(heat shock protein, HSP)이 용출된 것으로 판단하였다.養素) 이용율중(利用率中) 지방이용율은 대체로 일반식이 내의 륵지방(肋脂肪)보다는 지방질(脂肪質) 첨가식이내(添加食餌內)의 륵지방(肋脂肪)이 흡수율(吸收率)이나 이용률(利用率)이 더 우수함을 보여주었고, 근소축적률(筋素蓄積率)은 쥐에 있어서는 어유(魚油)군이 73.5%, 병아리에 있어서는 채종유군이 52.1%로 가장 높았으며 또한 쥐에서는 참기름군이 66.0%, 병아리에서는 대조구가 33.4로 가장 낮았으나 각 구별 통계적(統計的)인 차이는 없었다. 4. 쥐 실험(實驗)에서만 실시된 간지방(肝脂防) 함량측정(含量測定)은 채종유군의 그것이 다른 군보다 높았으며 옥수수기름, 콩기름, 참기름, 들기름, 동물유, 어유의 순서였으나 통계적(統計的)인 유의성(留意性)은 인정(認定)되지 않았고 일반적(一般的)으로 식물성 유지급여군의 간지방함량(肝脂肪含量)이 다른 군보다 높았다. 5. 혈청(血淸)콜레스테롤 함량(含量)은 쥐에 있어서는 채종유군이 가장 높았으며 참기름군이 비교적(比較的) 높은 수치(數値)를 나타냈고, 병아리실험에서는 동물유군이 어유, 콩기름, 참기름, 들기름, 옥수수기름, 채종유, 대조군보다 높았으나 통계적(統計的)인 유의차(留意差)는 없었다.6. 지방산조성(脂肪酸造成)은 동물성유지는 대체로 palmitic acid, myristic acid함량이 많았으며 식물성유는 Linoleic acid 와 oleic acid가 많았고 옥수수기름이 필수지방산인 Linoleic acid 함량이 54.7%로 가장많았으며 특히 들기름이 2중 결합 3개인 Linolenic acid가 58.4%로 다른 식물성기름보다 월등히 높았다. 한편 식물성 기름에는 Arachidonic acid 가 소량있으나 동물유(動物油)나 어유(魚油)에서는 분석(分析)되지 못했다.