• 제목/요약/키워드: MS2

검색결과 7,269건 처리시간 0.034초

A Comprehensive Identification of Synaptic Vesicle Proteins in Rat Brains by cRPLC/MS-MS and 2DE/MALDI-TOF-MS

  • Lee, Won-Kyu;Kim, Hye-Jung;Min, Hye-Ki;Kang, Un-Beom;Lee, Cheol-Ju;Lee, Sang-Won;Kim, Ick-Young;Lee, Seung-Taek;Kwon, Oh-Seung;Yu, Yeon-Gyu
    • Bulletin of the Korean Chemical Society
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    • 제28권9호
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    • pp.1499-1509
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    • 2007
  • Proteomic analyses of synaptic vesicle fraction from rat brain have been performed for the better understanding of vesicle regulation and signal transmission. Two different approaches were applied to identify proteins in synaptic vesicle fraction. First, the isolated synaptic vesicle proteins were treated with trypsin, and the resulting peptides were analyzed using a high-pressure capillary reversed phase liquid chromatography/tandem mass spectrometry (cRPLC/MS/MS). Alternatively, proteins were separated by two-dimensional gel electrophoresis (2DE) and identified by matrix-assisted laser desorption ionization mass spectrometry (MALDI-TOF/MS). Total 18 and 52 proteins were identified from cRPLC/MS-MS and 2DE-MALDI-TOF-MS analysis, respectively. Among them only 2 proteins were identified by both methods. Of the proteins identified, 70% were soluble proteins and 30% were membrane proteins. They were categorized by their functions in vesicle trafficking and biogenesis, energy metabolism, signal transduction, transport and unknown functions. Among them, 27 proteins were not previously reported as synaptic proteins. The cellular functions of unknown proteins were estimated from the analysis of domain structure, expression profile and predicted interaction partners.

조직배양을 이용한 처녀치마[Heloniopsis orientalis (Thunb) C. Tanaka] 대량 증식 (Micropropagation of Heloniopsis orientalis (Thunb.) C. Tanska in vitro)

  • 윤세영;이명선;임상철;신중두
    • 식물조직배양학회지
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    • 제27권3호
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    • pp.197-202
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    • 2000
  • 조직배양을 이용한 처녀치마 대량증식을 위한 적정배지, 생장조절제 및 농도구명을 위해 본 연구를 수행하였다. Shootb 및 roots분화의 경우 zeatin 3.0 mgι$^{-1}$을 첨가한 MS 배지에서 shoots및 roots 형성률이 각각 20, 30%로서 가장 양호한 것으로 나타났다. 1/2 MS배지의 경우 zeatin 1.0mgι$^{-1}$에서 shoots 형성률이 67 %, B5 배지에 있어서 zeatin 3.0 mgι$^{-1}$ 처리에서 33 %로 가장 양호한 것으로 나타났다. 배지에 따른 식물 생장조절제 처리에 따른 식물체 분화율은 MS 배지에서는 2,4-D 0.5 mgι$^{-1}$, 1/2 MS 배지에서 zeatin 1.0 mgι$^{-1}$ 및 B5 배지에서 reatin 3.0 mgι$^{-1}$에서 자장 가장 많은 100, 193, 280 및 310%의 분화된 식물체를 얻을 수 있었다. 전반적으로 야생화인 처녀치마의 잎 조직으로부터 multiple shoots을 유도하여 대량증식을 위한 목적으로는 B5 배지에 생장조절제인 zeatin 3.0 mgι$^{-1}$을 첨가시키는 것이 가장 효과적인 것으로 나타났다.

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MS 배지내 무기물 농도, 당 농도 및 광 조건이 무스카리의 기내 자구 형성과 비대에 미치는 영향 (Effect of MS Medium Strength, Sucrose Concentration, and Light Condition on Bulblet Formation and Growth of Muscari armenicum In Vitro)

  • 정미영;김창길;정재동
    • 화훼연구
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    • 제19권1호
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    • pp.49-54
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    • 2011
  • 본 연구는 우리나라 무스카리 우점품종인 'Early Giant'의 대량증식 체계를 구축하기 위하여 잎 절편으로부터 소인경 형성과 비대에 미치는 MS 무기염 농도, 당 농도 및 광조건의 영향을 조사하였다. 무스카리의 잎 절편을 2주간 암 배양 후 MS 기본배지에 NAA $0.01mg{\cdot}L^{-1}$, kinetin $0.2m{\cdot}L^{-1}$, 자당 $30g{\cdot}L^{-1}$와 gelrite $3g{\cdot}L^{-1}$가 첨가된 배지에 16시간 일장으로 명 배양하였을 때 자구형성 및 생육이 가장 양호하였다. 다만, 자구 비대는 MS 배지 내 $60g{\cdot}L^{-1}$ 당 농도에서 촉진되었다. 온실에서 순화된 식물체는 정상적으로 개화하였으며 정식 2년차에 1.5개 내외의 자구를 가진 구를 생산할 수 있었다.

LC/MS 데이터에서 동위 원소 패턴을 찾는 새로운 방법 (A New Method for Detecting Isotope Patterns in Liquid Chromatography/Mass Spectrometry Data)

  • Kim, Youn-Dong;Han, Joon-Hee;Hwang, Ji-Woon
    • 한국생물정보학회:학술대회논문집
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    • 한국생물정보시스템생물학회 2004년도 The 3rd Annual Conference for The Korean Society for Bioinformatics Association of Asian Societies for Bioinformatics 2004 Symposium
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    • pp.167-177
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    • 2004
  • 본 논문에서는 LC/MS 데이터로부터 동위 원소 패턴(isotope pattern)을 찾는 새로운 방법을 제시하고자 한다. 기존의 분석 방법에서는 LC/MS 데이터를 1차원적으로 분석하고 있기 때문에 2차원에서 적용할 수 있는 알고리즘을 적용하기가 어렵다. LC/MS 데이터를 2차원 영상으로 가시화해 본 결과, 하나의 동위 원소 패턴에 속하는 단일 동위 원소 피크(single isotope peak)는 모양, 크기와 같은 2차원 형태적 특징들도 유사함을 알 수 있다. 따라서, 기존의 방법들이 질량 스펙트럼과 같은 1차원 신호를 분석하는 것에 중점을 둔 것에 비해, 본 논문에서는 LC/MS 데이터를 2차원 신호 즉, 영상(image)으로 간주하고 영상 처리 방법과 객체 인식 방법을 적용하였다. 실험 결과 같은 동위 원소 패턴에 속하는 각각의 단일 동위원소 피크들 사이에 peak maxima position 뿐만 아니라 skewness, variance등도 유사였으며 이러한 유사도를 기반으로 동위 원소 패턴을 찾을 수 있었다.

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더블 샘플링 기법을 사용한 10bit 1MS/s 0.5mW 축차 비교형 아날로그-디지털 변환기 (A 10bit 1MS/s 0.5mW SAR ADC with Double Sampling Technique)

  • 이호규;김무영;김철우
    • 전기학회논문지
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    • 제60권2호
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    • pp.325-329
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    • 2011
  • This paper introduces the 10b 1MS/s SAR ADC with double sampling technique to reduce the power consumption. The SAR ADC is implemented in CMOS 1P8M 65nm technology and occupies 0.11um2. The maximum sampling rate is 1MS/s. The simulated SNDR and SFDR are 55.6dB and 62.7dB at 484kHz input frequency, respectively. The implemented data converter consumes 507uW with 1.2-V supply.

LC-MS/MS 시스템을 이용한 소변 중 N-니트로사민류 분석법 확립 (Analysis Method of N-Nitrosamines in Human Urine by LC-MS/MS System)

  • 박나연;정웅;고영림
    • 대한화학회지
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    • 제61권2호
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    • pp.51-56
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    • 2017
  • N-니트로사민은 이차 아민과 아질산이 산성조건 하에서 니트로소화 반응을 통해 생성되는 니트로소 화합물이다. 약 300여종이 존재하며, 그 중 90%가 동물실험을 통해 발암성이 있음이 확인되었다. 1987년 IARC에서 NDMA와 NDEA를 Group 2A로 지정하였고, NDPA, NDBA, NPYR, NPIP, NMOR을 Group 2B로 지정하였다. 본 연구에서는 N-니트로사민류의 생물학적 모니터링을 위하여 소변 중 N-니트로사민류의 분석법을 확립하였다. 소변시료는 고체상추출(Solid phase extraction, SPE)을 통하여 전처리 한 후, LC-(APCI)-MS/MS를 이용하여 정량분석 하였다. 확립된 분석법의 정확도는 85.8~110.2% 이었고, 정밀도는 1.1~10.5%로 나타났다. 검출한계는 0.0002 (NDBA) ~ 0.0793 (NDMA) ng/ml 이었고, 검량선 회귀식의 상관계수($r^2$)은 0.999 이상으로 우수한 직선성을 보여주었다. 실제 소변 중 N-니트로사민류의 평균 농도는 NDMA 2.645 mg/g creatinine, NDEA 0.067 mg/g creatinine, NMEA 0.009 mg/g creatinine, NDBA 0.011 mg/g creatinine, NPIP 0.271 mg/g creatinine, NPYR 0.413 mg/g creatinine 이고, NDPA와 NMOR은 검출되지 않았다. 추후 N-니트로사민류의 인체 노출량 평가 및 위해평가를 위한 기기분석방법으로 활용될 수 있을 것으로 판단된다.

LC-MS/MS를 이용한 곽향정기산(藿香正氣散) 추출물 중 20종 성분의 함량분석 (Quantitative Analysis of the Twenty Marker Components in Gwakhyangjeonggi-san using Ultra-Performance Liquid Chromatography with Mass Spectrometer)

  • 서창섭;신현규
    • 생약학회지
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    • 제45권2호
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    • pp.113-120
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    • 2014
  • Generally, Gwakhyangjeonggi-san has been used for treatment of diarrhea-predominant irritable bowel syndrome. In this study, an ultra-performance liquid chromatography-electrospray ionization-mass spectrometer method was established for the simultaneous quantification of marker compounds 1-20 in Gwakhyangjeonggi-san water extract. All analytes were separated by gradient elution using two mobile phases on a UPLC BEH $C_{18}$ ($100{\times}2.1mm$, $1.7{\mu}m$) column and maintained at $45^{\circ}C$. The injection volume was $2.0{\mu}L$ and the flow rate was 0.3 mL/min with detection at mass spectrometer. Regression equations of the compounds 1-20 were acquired with $r^2$ values ${\geq}0.9950$. The values of limit of detection and quantification of all analytes were 0.01-2.79 ng/mL and 0.03-8.37 ng/mL, respectively. The amounts of the compounds 1-20 in Gwakhyangjeonggi-san water extract were not detected $-3,236.67{\mu}g/g$. The established LC-MS/MS methods will be valuable to improve quality control of traditional herbal formula, Gwakhyangjeonggi-san.

Simultaneous Quantification of 13 Ginsenosides by LC-MS/MS and its Application in Diverse Ginseng Extracts

  • Jo, Jung Jae;Cho, Pil Joung;Lee, Sangkyu
    • Mass Spectrometry Letters
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    • 제9권2호
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    • pp.41-45
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    • 2018
  • Ginseng (Panax ginseng Meyer) has been used as traditional herbal drug in Asian countries. Ginsenosides are major components having pharmacological and biological efficacy like anti-inflammatory, anti-diabetic and anti-tumor effects. To control the quality of the components in diverse ginseng products, we developed a new quantitative method using LC-MS/MS for 13 ginsenosides; Rb1, Rb2, Rc, Rd, Re, Rf, 20(S)-Rh1, 20(S)-Rh2, Rg1, 20(S)-Rg3, F1, F2, and compound K. This method was successfully validated for linearity, precision, and accuracy. This quantification method applied in four representative ginseng products; fresh ginseng powder, white ginseng powder, red ginseng extract powder, and red ginseng extract. Here the amounts of the 13 ginsenosides in the various type of ginseng samples could be analyzed simultaneously and expected to be suitable for quality control of ginseng products.

Effect of Plant Growth Regulators on Plant Regeneration and in vitro Flowering Through Somatic Embryogenesis of Gentiana scabra

  • Kim Young-Sook;Choi Chang-Hak;Kim Hyun-Soon;Ko Jeong-Ae
    • Plant Resources
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    • 제8권2호
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    • pp.81-86
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    • 2005
  • An efficient plant regeneration system of Gentiana scabra through somatic embryogenesis was established. Leaves and roots of seedlings of Gentiana scabra excised after germination were cultured on MS basal medium with 2,4-D, NAA or BA. Embryogenic callus was obtained on MS medium with 0.5 mg/L 2,4-D alone or 0.1 mg/L 2,4-D combimation with 1.0 mg/L BA after 45 days of culture. These embryogenic calli gave rise to somatic embryos, which subsequently developed into plantlets on MS medium without PGRs. Also, shoots were effectively differentiated from embryogenic callus when root segments were cultured on MS medium supplement with 0.1 mg/L 2,4-D and 1.0 mg/L BA. Shoots were effectively rooted on MS medium without PGRs. In vitro flowers were formed from plantlets cultured on MS medium with $5\%$ sucrose after 60 days of culture.

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LC-MS/MS를 이용한 담배 중 Amadori Compounds의 분석 (Analysis of Amadori Compounds in Tobacco Leaf by LC-MS/MS)

  • 민혜정;김영회;이정민;장기철
    • 한국연초학회지
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    • 제33권1호
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    • pp.21-27
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    • 2011
  • Amadori compounds(1-deoxy-1-amino-2-ketoses) are important precursors of color, flavor and aroma produced in foods. Amadori compounds occur naturally in tobacco. The contribution of amadori compounds to smoke quality has been (of) interest because of their roles of the Maillard reaction in the leaf chemistry. The amounts of these compound in tobacco are affected by the processes of aging, drying and storage conditions. In this study, eight compounds were chemically synthesized because amadori compounds (have not been sold commercially these days.) were not available for obtaining commercially. The aim of this study was to develop the analytical method of amadori compounds in tobacco leaf by the liquid chromatography mass spectrometry using triple quadrupole analyzer(LC-MS/MS). This method was simple, rapid, selective and sensitive, and eight amadori compounds were simultaneously and quantitatively analyzed within 20 minutes. This method showed excellent accuracy and precision. Recovery rates of amadori compounds ranged from 86% to 102%, with relative standard deviation(RSD) ranged from 2.6% to 5.9%. This method was applied to analysis of amadori compounds contents of tobacco leaves in different varieties. Furthermore, it was expected that the method could be extended to the analysis of other amadori compounds.