• 제목/요약/키워드: Fluorescence.

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근적외선-II 형광 이미징을 위한 무기 나노입자 (Inorganic Nanoparticles for Near-infrared-II Fluorescence Imaging)

  • 박용일
    • 공업화학
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    • 제33권1호
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    • pp.17-27
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    • 2022
  • 형광 이미징은 시간 분해능과 공간 해상도가 높기 때문에 기초연구에서 세포나 소동물 이미징에 널리 활용된다. 기존의 형광 이미징은 가시광선 영역의 광원을 활용하기 때문에 조직 내 광투과도가 낮고, 광원에 의한 광독성이 생길 수 있으며, 자가형광에 의한 간섭으로 검출 민감도가 떨어지는 한계가 있다. 이러한 점을 개선하기 위해 에너지가 낮은 장파장의 광원을 활용하고자 하며, 700~900 nm 영역을 활용하는 근적외선-I 형광 이미징이 개발되었고, 이미징 성능을 대폭 향상시키기 위해서 1000~1700 nm 영역의 장파장을 이용하는 근적외선-II 이미징이 연구자들의 관심을 받고 있다. 근적외선-II 영역은 광산란이 최소화되어 생체조직 내 투과도를 약 10 mm까지 향상시킬 수 있고, 생체조직의 자가형광도 최소화되어 고민감도와 고해상도의 형광 이미징이 가능하다. 본 총설에서는 다양한 근적외선-II 형광 이미징 탐침 중에서 광안정성이 뛰어나고 발광 파장 조절이 용이한 무기 나노입자 기반 탐침에 대해 살펴보았고, 그 중에서 단층 탄소 나노튜브와 양자점 및 란탄족 나노입자에 대해 중점적으로 기술하였다.

Effect of degumming conditions on the fluorescence intensity of fluorescent silk cocoons: A combined experimental and molecular dynamics study

  • Chan Yeong, Yu;Ezekiel Edward, Nettey-Oppong;Elijah, Effah;Su Min, Han;Seong-Wan, Kim;Seung Ho, Choi
    • International Journal of Industrial Entomology and Biomaterials
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    • 제45권2호
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    • pp.56-69
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    • 2022
  • Silk is a unique natural biopolymer with outstanding biocompatibility, high mechanical strength, and superior optical transparency. Due to its excellent properties, silk has been widely reported as an ideal biomaterial for several biomedical applications. Recently, fluorescent silk protein, a variant of native silk, has been reported as a biophotonic material with the potential for bioimaging and biosensing. Despite the realization of fluorescent silk, the traditional degumming process of fluorescence silk is crude and often results in fluorescence loss. The loss of fluorescent properties is attributed to the sensitivity of silk fibroin to temperature and solvent concentration during degumming. However, there is no comprehensive information on the influence of these processing parameters on fluorescence evolution and decay during fluorescent silk processing. Therefore, we conducted a spectroscopic study on fluorescence decay as a function of temperature, concentration, and duration for fluorescent silk cocoon degumming. Sodium carbonate solution was tested for degumming the fluorescent silk cocoons with different concentrations and temperatures; also, sodium carbonate solution is combined with Alcalase enzyme and triton x-100 to find optimal degumming conditions. Additionally, we conducted a molecular dynamics study to investigate the fundamental effect of temperature on the stability of the fluorescent protein. We observed degumming temperature as the prime source of fluorescent intensity reduction. From the MD study, fluorescence degradation originated from the thermal agitation of fluorescent protein Cα atoms and fluctuations of amino acid residues located in the chromophore region. Overall, degumming fluorescent silk with sodium carbonate and Alcalase enzyme solution at 25 ℃ preserved fluorescence.

Photoinhibition Induced Alterations in Energy Transfer Process in Phycobilisomes of PS II in the Cyanobacterium, Spirulina platensis

  • Kumar, Duvvuri Prasanna;Murthy, Sistla D.S.
    • BMB Reports
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    • 제40권5호
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    • pp.644-648
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    • 2007
  • Exposure of algae or plants to irradiance from above the light saturation point of photosynthesis is known as high light stress. This high light stress induces various responses including photoinhibition of the photosynthetic apparatus. The degree of photoinhibition could be clearly determined by measuring the parameters such as absorption and fluorescence of chromoproteins. In cyanobacteria and red algae, most of the photosystem (PS) II associated light harvesting is performed by a membrane attached complex called the phycobilisome (PBS). The effects of high intensity light (1000-4000 ${\mu}mol$ photons $m^{-2}s^{-1}$) on excitation energy transfer from PBSs to PS II in a cyanobacterium Spirulina platensis were studied by measuring room temperature PC fluorescence emission spectra. High light (3000 ${\mu}mol$ photons $m^{-2}s^{-1}$) stress had a significant effect on PC fluorescence emission spectra. On the other hand, light stress induced an increase in the ratio of PC fluorescence intensity of PBS indicating that light stress inhibits excitation energy transfer from PBS to PS II. The high light treatment to 3000 ${\mu}mol$ photons $m^{-2}s^{-1}$ caused disappearance of 31.5 kDa linker polypeptide which is known to link PC discs together. In addition we observed the similar decrease in the other polypeptide contents. Our data concludes that the Spirulina cells upon light treatment causes alterations in the phycobiliproteins (PBPs) and affects the energy transfer process within the PBSs.

모바일용 형광이미지 분석 통합관리 시스템 개발 (Development of An Integration Management System of Analyzing Fluorescence Images on Smart Phone)

  • 조미경;심재술
    • 한국정보통신학회:학술대회논문집
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    • 한국정보통신학회 2012년도 춘계학술대회
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    • pp.916-919
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    • 2012
  • 분자 수준의 크기인 세포 내에서 일어나는 현상들을 영상화하는 바이오 이미징 분야는 단백질이나 DNA 등에서 일어나는 현상까지도 공초점 형광현미경을 이용하여 영상으로 또렷이 관찰할 수 있는 수준으로 발전하였다. 따라서 생체 형광 이미징 분야는 진단과 치료를 위해 의료 임상 분야에서 필수적으로 사용되고 있다. 본 논문에서는 시공간의 제약을 받지 않고 형광 이미지를 분석할 수 있는 모바일용 형광이미지 분석통합 관리 시스템을 개발하였다. 개발된 시스템은 서버 클라이언트 기반이며 형광이미지의 강도 값을 분석하고 통합 관리하기 위한 기능을 제공한다. 본 시스템은 의료인이 언제 어디에서나 응급환자의 형광이미지 사진을 분석하여 진단을 내릴 수 있도록 돕기 때문에 유비쿼터스 헬스를 구현하기 위한 수단이 된다.

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Acridine Fluorescence Behaviors in Different Polymeric Microenvironments Directed by C2-Proton-Acidity of Imidazolium-Based Ionic Liquids

  • Ji, Myoung-Jin;Kim, Jong-Gyu;Shin, Ueon-Sang
    • Bulletin of the Korean Chemical Society
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    • 제33권8호
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    • pp.2489-2493
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    • 2012
  • A new fluorescent system (acridine/RTIL hybrid gel) confined in the 3D micro-structure of a poly(lactic acid) membrane were prepared from 1-butyl-3-methylimidazolium-based ionic liquids ([bmim]X (X = $SbF_6$, $NTf_2$, Cl); RTILs), poly(lactic acid) (PLA), and acridine via the sol-gel route. SEM images showed that, in the presence of [bmim]$SbF_6$ and [bmim]$NTf_2$, 3D-ly paticulated structures were created inside the PLA membranes and acridine/RTIL hybrid gels were confined in gabs of particulates. However, the use of [bmim]Cl induced the formation of a 3D-ly porous structure containing the hybrid gel of acridine/[bmimCl in the micropores. The three fluorescent systems exhibited different fluorescence behaviors (fluorescence maximum and intensity) depending on the C2-H acidity scale of the RTILs (or their anion type). Acridine gels hybridized with [bmim]$SbF_6$ and [bmim]$NTf_2$ showed blue fluorescence with relative high intensity, whereas the hybrid gel with [bmim]Cl exhibited almost no fluorescence under dry conditions. However, the acridine/[bmim]Cl hybrid system in the micro-porous PLA membrane started to emit fluorescent light under humid conditions and showed a possible response, indicating that it could be applied as a humidity sensor.

Spectrofluorometric Properties of N-Terminal Domain of Lumazine Protein from Photobacterium leiognathi

  • Kang, Kyoung-Suk;Kim, So-Young;Lee, Jung-Hwan;Nam, Ki-Seok;Lee, Eui Ho;Lee, Chan Yong
    • Bulletin of the Korean Chemical Society
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    • 제34권6호
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    • pp.1673-1678
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    • 2013
  • Lumazine protein is a member of the riboflavin synthase superfamily and the intense fluorescence is caused by non-covalently bound to 6,7-dimethyl 8-ribityllumazine. To figure out the binding modes and the structure of the N-terminal domain of lumazine protein, the wild type of protein extending to amino acid 118 (N-LumP 118 Wt) and mutants of N-LumP 118 V41W, S48W, T50W, D64W, and A66W from Photobacterium leiognathi were purified. The biochemical properties of the wild type and mutants of N-LumP 118 proteins were analyzed by absorbance and fluorescence spectroscope. The peak of absorbance and fluorescence of lumazine ligand were shifted to longer wavelength on binding to N-LumPs. The observed absorbance value at 410 nm of lumazine bound to N-LumP 118 proteins indicate that one mole of N-LumP 118 proteins bind to one mole of ligand of lumazine. Fluorescence analysis show that the maximum peak of fluorescence of N-LumP S48W was shifted to the longest wavelength by binding with 6,7-dimethyl 8-ribityllumazine and was shown to the greatest quench effect by acrylamide among all tryptophan mutants.

형광현미경적 기법에 의한 대추나무, 뽕나무 및 일일초의 마이코플라스마 감염진단 (Fluorescence Microscopic Diagnosis of Mycoplasma Infections in Jujube, Mulberry and Periwinckle Plants)

  • 박원철;나용준
    • 한국식물병리학회지
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    • 제1권1호
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    • pp.12-16
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    • 1985
  • 마이코플라스마에 감염된 대추나무, 뽕나무 및 일일초의 조직절편을 형광염색소인 DAPI(4'-6-diamidino-2-phenylindole$\cdot$2HCl), aniline blue 그리고 quinacrine(quinacrine mustard dihydrochloride)으로 염색하여 형광현미경하에서 관찰함으로서 이들 형광염색소의 마이코프라스마 감염진단에의 효용가치를 비교 조사하였다. 이병식물의 줄기절편의 절부에서 특이형광반응이 나타났으나 건전식물의 조직절편에서는 특이형광반응이 관찰되지 않음으로써, DAPI, anilinc blue 및 quinacrine 등의 형광염색소에 의한 조직염색법은 대추나무, 뽕나무 및 일일초의 마이코플라스마 감염을 식속 정확하게 진단하는 데 매우 유용한 방법임을 보여주었다. 한펀, 이들 형광염색소 중에서는 DAPI가 가장 효과적이었다.

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Detecting Drought Stress in Soybean Plants Using Hyperspectral Fluorescence Imaging

  • Mo, Changyeun;Kim, Moon S.;Kim, Giyoung;Cheong, Eun Ju;Yang, Jinyoung;Lim, Jongguk
    • Journal of Biosystems Engineering
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    • 제40권4호
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    • pp.335-344
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    • 2015
  • Purpose: Soybean growth is adversely affected by environmental stresses such as drought, extreme temperatures, and nutrient deficiency. The objective of this study was to develop a method for rapid measurement of drought stress in soybean plants using a hyperspectral fluorescence imaging technique. Methods: Hyperspectral fluorescence images were obtained using UV-A light with 365 nm excitation. Two soybean cultivars under drought stress were analyzed. A partial least square regression (PLSR) model was used to predict drought stress in soybeans. Results: Partial least square (PLS) images were obtained for the two soybean cultivars using the results of the developed model during the period of drought stress treatment. Analysis of the PLS images showed that the accuracy of drought stress discrimination in the two cultivars was 0.973 for an 8-day treatment group and 0.969 for a 6-day treatment group. Conclusions: These results validate the use of hyperspectral fluorescence images for assessing drought stress in soybeans.