• 제목/요약/키워드: proteomic

검색결과 502건 처리시간 0.022초

Dehydroascorbate reductase 과발현 형질전환 감자 식물체의 단백질체 분석 (Proteomic analysis of dehydroascorbate reductase transgenic potato plants)

  • 한은희;구영민;김윤희;이신우
    • Journal of Plant Biotechnology
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    • 제43권2호
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    • pp.223-230
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    • 2016
  • 아스코르빈산(ascorbic acid, AsA)는 강력한 항산화 물질 및 환원제로서 식물에서 산화형 AsA인 dehydroascorbate(DHA)를 활성형인 환원형 AsA로 변환시키는 효소인 dehydroascorbate reductase (DHAR)에 의해 생성된다. 선행연구의 결과로서, 본 연구팀은 참깨의 모상근에서 분리한 DHAR 유전자를 이용하여 항시 발현하는 CaMV 35S 프로모터와 괴경 특이적으로 발현하는 patatin 프로모터의 조절하에 과발현 시킨 형질전환 감자를 개발하였다. 형질전환 감자 식물체들은 비형질전환체 보다 증가된 DHAR 활성과 AsA 함량을 보인 바 있다. 본 연구에서는 단백질체 분석을 통해서 형질전환 감자 식물체에서 DHAR 과발현에 의해 조절되는 단백질들을 조사하였다. 단백질체 분석의 결과로서, 형질전환 감자에서 도입된 DHAR 단백질과 다양한 항산화 관련 단백질들이 식물 생장시기 동안 증가 하였다. 본 연구의 결과로서, 도입된 유전자인 DHAR이 항산화 단백질들의 발현 증가를 통해 형질전환 식물체의 스트레스 내성 기작을 향상 시킬 수 있을 것으로 생각된다.

Identification of the novel substrates for caspase-6 in apoptosis using proteomic approaches

  • Cho, Jin Hwa;Lee, Phil Young;Son, Woo-Chan;Chi, Seung-Wook;Park, Byoung Chul;Kim, Jeong-Hoon;Park, Sung Goo
    • BMB Reports
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    • 제46권12호
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    • pp.588-593
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    • 2013
  • Apoptosis, programmed cell death, is a process involved in the development and maintenance of cell homeostasis in multicellular organisms. It is typically accompanied by the activation of a class of cysteine proteases called caspases. Apoptotic caspases are classified into the initiator caspases and the executioner caspases, according to the stage of their action in apoptotic processes. Although caspase-3, a typical executioner caspase, has been studied for its mechanism and substrates, little is known of caspase-6, one of the executioner caspases. To understand the biological functions of caspase-6, we performed proteomics analyses, to seek for novel caspase-6 substrates, using recombinant caspase-6 and HepG2 extract. Consequently, 34 different candidate proteins were identified, through 2-dimensional electrophoresis/MALDI-TOF analyses. Of these identified proteins, 8 proteins were validated with in vitro and in vivo cleavage assay. Herein, we report that HAUSP, Kinesin5B, GEP100, SDCCAG3 and PARD3 are novel substrates for caspase-6 during apoptosis.

대량의 프로테옴 데이타를 효과적으로 해석하기 위한 기계학습 기반 시스템 (An Effective Data Analysis System for Improving Throughput of Shotgun Proteomic Data based on Machine Learning)

  • 나승진;백은옥
    • 한국정보과학회논문지:소프트웨어및응용
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    • 제34권10호
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    • pp.889-899
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    • 2007
  • 최근 프로테오믹스 분야에서 단백질의 추출, 분리기술의 발전과 고성능 질량분석 장비로 인하여 대량으로, 또 빠르게 샘플을 분석하는 것이 가능해짐에 따라서, 한번의 실험으로부터 얻어지는 실험데이타의 양이 대폭 늘어나게 되었다. 따라서 대량의 데이타를 어떻게 처리하여 필요한 정보만을 얻어내는가가 큰 이슈가 되고 있다. 하지만 기존의 데이타 해석과정은 불필요하게 계산자원을 낭비하는 요소를 상당 부분을 포함하고 있고, 이로 인해 데이타 해석 시간이 증가함은 물론, 종종 옳지 않은 해석 결과를 생성함으로써 결과에 대한 신뢰도의 저하를 초래했다. 본 논문에서는 기존의 데이타 해석 과정에서의 문제점을 지적하고, 데이타 처리의 효율을 높임과 동시에 해석 결과의 신뢰도를 제고하기 위한 SIFTER 시스템을 제안한다. SIFTER 시스템은 본격적인 데이타 해석에 앞서, 질량 스펙트럼의 질을 평가하고 하전량을 결정하는 소프트웨어를 제공한다. 탠덤 질량 스펙트럼에 나타나는 단편 이온의 특성을 고려하여 스펙트럼의 질과 하전량을 정확하게 결정하는 방법을 제공함으로써, 데이타 해석에 앞서 스펙트럼의 질이 낮아 해석이 불가능할 것이 분명한 경우 이들을 미리 제거하고 스펙트럼 해석과정에 잘못된 정보가 사용되지 않도록 한다. 결과적으로 데이타 해석과정에서의 효율과 해석결과의 정확성에 있어 대폭적인 개선을 기대할 수 있다.

Proteomic Changes in Chick Brain Proteome Post Treatment with Lathyrus Sativus Neurotoxin, β-N-Oxalyl-L-α,β-Diaminopropionic Acid (L-ODAP): A Better Insight to Transient Neurolathyrism

  • Anil Kumar, D;Natarajan, Sumathi;Omar, Nabil A M Bin;Singh, Preeti;Bhimani, Rohan;Singh, Surya Satyanarayana
    • Toxicological Research
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    • 제34권3호
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    • pp.267-279
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    • 2018
  • Neurolathyrism is a neurodegenerative disorder characterized by spastic paraplegia resulting from the excessive consumption of Lathyrus sativus (Grass pea). ${\beta}$-N-Oxalyl-L-${\alpha},{\beta}$-diaminopropionic acid (L-ODAP) is the primary neurotoxic component in this pea. The present study attempted to evaluate the proteome-wide alterations in chick brain 2 hr and 4 hr post L-ODAP treatment. Proteomic analysis of chick brain homogenates revealed several proteins involved in cytoskeletal structure, signaling, cellular metabolism, free radical scavenging, oxidative stress and neurodegenerative disorders were initially up-regulated at 2 hr and later recovered to normal levels by 4 hr. Since L-ODAP mediated neurotoxicity is mainly by excitotoxicity and oxidative stress related dysfunctions, this study further evaluated the role of L-ODAP in apoptosis in vitro using human neuroblastoma cell line, IMR-32. The in vitro studies carried out at $200{\mu}M$ L-ODAP for 4 hr indicate minimal intracellular ROS generation and alteration of mitochondrial membrane potential though not leading to apoptotic cell death. L-ODAP at low concentrations can be explored as a stimulator of various reactive oxygen species (ROS) mediated cell signaling pathways not detrimental to cells. Insights from our study may provide a platform to explore the beneficial side of L-ODAP at lower concentrations. This study is of significance especially in view of the Government of India lifting the ban on cultivation of low toxin Lathyrus varieties and consumption of this lentil.

Proteomic Analysis of Haptoglobin and Amyloid A Protein Levels in Patients with Vivax Malaria

  • Bahk, Young-Yil;Na, Byoung-Kuk;Cho, Shin-Hyeong;Kim, Jung-Yeon;Lim, Kook-Jin;Kim, Tong-Soo
    • Parasites, Hosts and Diseases
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    • 제48권3호
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    • pp.203-211
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    • 2010
  • Advancements in the field of proteomics have provided great opportunities for the development of diagnostic and therapeutic tools against human diseases. In this study, we analyzed haptoglobin and amyloid A protein levels of vivax malaria patients with combinations of depletion of the abundant plasma proteins, 2-dimensional gel electrophoresis (2-DE), image analysis, and mass spectrometry in the plasma between normal healthy donors and vivax malaria patients. The results showed that the expression level of haptoglobin had become significantly lower or undetectable in the plasma of vivax malaria patients due to proteolytic cleavage when compared to healthy donors on 2-DE gels. Meanwhile, serum amyloid A protein was significantly increased in vivax malaria patient's plasma with high statistical values. These 2 proteins are common acute phase reactants and further large scale evaluation with a larger number of patient's will be necessary to establish the possible clinical meaning of the existential changes of these proteins in vivax malaria patients. However, our proteomic analysis suggests the feasible values of some plasma proteins, such as haptoglobin and serum amyloid A, as associating factor candidates for vivax malaria.

Proteomic Analysis of Toxoplasma gondii KI-1 Tachyzoites

  • Choi, Si-Hwan;Kim, Tae-Yun;Park, Sung-Goo;Cha, Guang-Ho;Shin, Dae-Whan;Chai, Jong-Yil;Lee, Young-Ha
    • Parasites, Hosts and Diseases
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    • 제48권3호
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    • pp.195-201
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    • 2010
  • We studied on the proteomic characteristics of Toxoplasma gondii KI-1 tachyzoites which were originally isolated from a Korean patient, and compared with those of the well-known virulent RH strain using 2-dimensional electrophoresis (2-DE), mass spectrometry, and quantitative real-time PCR. Two-dimensional separation of the total proteins isolated from KI-1 tachyzoites revealed up to 150 spots, of which 121 were consistent with those of RH tachyzoites. Of the remaining 29 spots, 14 showed greater than 5-fold difference in density between the KI-1 and RH tachyzoites at a pH of 5.0-8.0. Among the 14 spots, 5 from the KI-1 isolate and 7 from the RH strain were identified using MALDI-TOF mass spectrometry and database searches. The spots from the KI-1 tachyzoties were dense granule proteins (GRA 2,3,6, and 7), hypoxanthine-guanine-xanthine phosphoribosyltransferase (HGRPTase), and uracil phosphoribosyltransferase (UPRTase). The spots from the RH strain were surface antigen 1 (SAG 1), L-lactate dehydrogenase (LDH), actin, chorismate synthase, peroximal catalase, hexokinase, bifunctional dihydrofolate reductase-thymidylate synthase (DHTR-TS), and nucleosidetriphosphatases (NTPases). Quantitative real-time PCR supported our mass spectrometric results by showing the elevated expression of the genes encoding GRA 2,3, and 6 and UPRTase in the KI-1 tachyzoites and those encoding GRA 7, SAG 1, NTPase, and chorismate synthase in the RH tachyzoites. These observations demonstrate that the protein compositions of KI-1 and RH tachyzoites are similar but differential protein expression is involved in virulence.

Comparative proteomic analysis of plant responses to sound waves in Arabidopsis

  • Kwon, Young Sang;Jeong, Mi-Jeong;Cha, Jaeyul;Jeong, Sung Woo;Park, Soo-Chul;Shin, Sung Chul;Chung, Woo Sik;Bae, Hanhong;Bae, Dong-Won
    • Journal of Plant Biotechnology
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    • 제39권4호
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    • pp.261-272
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    • 2012
  • Environmental factors greatly influence the growth, development, and even genetic characteristics of plants. The mechanisms by which sound influences plant growth, however, remain obscure. Previously, our group reported that several genes were differentially regulated by specific frequenciesof sound treatmentusing a sound-treated subtractive library. In this study, we used a proteomic approach to investigate plant responses to sound waves in Arabidopsis. The plants were exposed to 250-Hz or 500-Hz sound waves, and total proteins were extracted from leaves 8 h and 24 h after treatment. Proteins extracted from leaves were subjected to 2-DE analysis. Thirty-eight spots were found to be differentially regulated in response to sound waves and were identified using MALDI-TOF MS and MALDI-TOF/TOF MS. The functions of the identified proteins were classified into photosynthesis, stress and defense, nitrogen metabolism, and carbohydrate metabolism. To the best of our knowledge, this is the first report on the analysis of protein changes in response to sound waves in Arabidopsis leaves. These findings provide a better understanding of the molecular basis of responses to sound waves in Arabidopsis.

Annexin A5 as a New Potential Biomarker for Cisplatin-Induced Toxicity in Human Kidney Epithelial Cells

  • Kwon, Yeo-Jung;Jung, Jin-Joo;Park, Na-Hee;Ye, Dong-Jin;Kim, Donghak;Moon, Aree;Chun, Young-Jin
    • Biomolecules & Therapeutics
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    • 제21권3호
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    • pp.190-195
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    • 2013
  • Cisplatin is a member of platinum-containing anti-cancer drugs that causes cross-linking of DNA and ultimately cancer cell apoptosis. The therapeutic function of cisplatin on various types of cancers has been widely reported but the side effects have been discovered together and nephrotoxicity has been regarded as major side effect of cisplatin. To select candidates for new sensitive nephrotoxicity biomarker, we performed proteomic analysis using 2-DE/MALDI-TOF-MS followed by cisplatin treatment in human kidney cell line, HK-2 cells, and compared the results to the gene profile from microarray composed of genes changed in expression by cisplatin from formerly reported article. Annexin A5 has been selected to be the most potential candidate and it has been identified using Western blot, RT-PCR and cell viability assay whether annexin A5 is available to be a sensitive nephrotoxic biomarker. Treatment with cisplatin on HK-2 cells caused the increase of annexin A5 expression in protein and mRNA levels. Over-expression of annexin A5 blocked HK-2 cell proliferation, indicating correlation between annexin A5 and renal cell toxicity. Taken together, these results suggest the possibility of annexin A5 as a new biomarker for cisplatin-mediated nephrotoxicity.

Proteomic analysis of rice mutants susceptible to Magnaporthe oryzae

  • Ryu, Hak-Seung;Song, Min-Young;Kim, Chi-Yeol;Han, Muho;Lee, Sang-Kyu;Ryoo, Nayeon;Cho, Jung-Il;Hahn, Tae-Ryong;Jeon, Jong-Seong
    • Plant Biotechnology Reports
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    • 제3권2호
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    • pp.167-174
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    • 2009
  • To identify genes involved in rice Pi5-mediated disease resistance to Magnaporthe oryzae, we compared the proteomes of the RIL260 rice strain carrying the Pi5 resistance gene with its susceptible mutants M5465 and M7023. Proteins were extracted from the leaf tissues of both RIL260 and the mutant lines at 0, 24, and 48 h after M. oryzae inoculation and separated by two-dimensional polyacrylamide gel electrophoresis (2-DE). Matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis identified eight proteins that were differently expressed between the resistant and susceptible plants (three down- and five up-regulated proteins in the mutants). The down-regulated proteins included a triosephosphate isomerase (spot no. 2210), a 2,3-bisphosphoglycerate-independent phosphoglycerate mutase (no. 3611), and an unknown protein (no. 4505). In addition, the five up-regulated proteins in the mutants were predicted to be a fructokinase I (no. 313), a glutathione S-transferase (no. 2310), an atpB of chloroplast ATP synthase (no. 3616), an aminopeptidase N (no. 3724), and an unknown protein (no. 308). These results suggest that proteomic analysis of rice susceptible mutants is a useful method for identifying novel proteins involved in resistance to the M. oryzae pathogen.

2H-Gel 이미지의 정렬 및 클러스터링 (Clustering of 2D-Gel images)

  • 허원
    • KSBB Journal
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    • 제20권2호
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    • pp.71-75
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    • 2005
  • 2D-Gel 이미지간의 유사성을 기준으로 생물학적인 시료가 프로테옴 수준에서 유사성의 정도와 서로 다른 단백질 스팟을 파악해 낼 수 있다. 그러나 생물학적인 시료는 개체간 변화가 크고 2차원 전기영동장치의 재현성의 한계로 인하여 비교가 어려운 경우가 많고 의미 없는 차이점만 발견되는 경우 또한 비일비재하다. 이를 극복하기 위해서는 프로테옴 이미지간의 정렬을 통하여 정확한 비교가 가능하게 하여야한다. 본 연구에서는 이미지상의 단백질 스팟을 일일이 찾지 않고 여러 개의 원시 이미지를 동시에 정렬시키는 multiresolution-multilevel algorithm을 활용하여 소프트웨어를 개발하였다. 또 이렇게 정렬된 이미지들이 서로 얼마나 유사한지 보여주는 Phylogenetic tree를 자동으로 생성시키는 소프트웨어를 개발하였다. 이 방법을 이용하여 Fetal Alcohol Syndrome의 case와 control의 10개의 프로테옴 이미지에 대하여 클러스터링을 시도하였다. 이와 같이 2D-Gel 프로테옴 전체의 이미지를 비교하여 유사한 정도에 따라 모으는 클러스터링은 FAS 시료의 경우 case와 control 보다는 시료원의 외연적인 특징인 나이 혹은 성별에 더 의하여 의존하는 것으로 나타났다.