• 제목/요약/키워드: lectin

검색결과 374건 처리시간 0.037초

대두(Glycine max L.)의 렉틴 분리 및 특성 (Isolation and Characterization of Lectin in Soybean(Glycine max L.))

  • 박원목;이용세;박상호;김성환;윤경은
    • 한국작물학회지
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    • 제34권2호
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    • pp.120-126
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    • 1989
  • 본 실험은 대두(Glycine max L.) 방사품종의 종자단백질에서 렉틴을 분리하여 그 특성을 조사하기 위하여 수행되었다. 렉틴의 분리방법은 (NH$_4$)$_2$SO$_4$의 50~80% 포화침전단백질을 Carboxymethyl cellulose column과 Sephadex G 100 column을 거쳐서 분리, 정제되었다. 순도의 검정은 2~30% polyacrylamide porosity gradient gel을 사용한 전기영동법으로 단일 band를 확인하였고 또한 분자량은 11% sodium dodecyl sulfate polyacrylamide gel에 의하여 134,000 dalton임을 추정하였으며 45,000 dalton의 3개의 subunits로 구성되어 있음을 알았다. Schiff reagent에 의하여 분홍색 반응을 일으켰으므로 이것은 당단백질임을 알 수 있었다. 본 당단백질은 토끼와 사람의 적혈구 모두에서 적혈구응집 반응이 일어났으며 사람의 혈액형중에서 적형구응집 정도는 A>B>O>AB형의 순서로 응집이 잘 일어났다. 당류에 의한 적혈구응집저해는 N -acetyl-D-galactoseamine 과 D-galactose에 의하여 일어났다.

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Mannan-binding lectin of the sea cucumbers Stichopus japonicus has common antigenic determinants with human serum mannan-binding lectin

  • Bulgakov, A.A.;Petrova, I.Yu.;Vakhrusheva, N.M.;Eliseikina, M.G.
    • 한국어업기술학회:학술대회논문집
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    • 한국어업기술학회 2000년도 춘계수산관련학회 공동학술대회발표요지집
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    • pp.530-530
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    • 2000
  • The host defense system or immune system of all modern animals has their roots in very ancient organisms. After analyzing literature data concerning properties of invertebrates and vertebrates lectins we suggest that mechanism of mannans recognition may exist in marine invertebrates, as a universal mechanism for homeostasis maintenance and host defense, and mannan-binding lectins family of vertebrates has ancient precursor, as was shown for another S-type lectins family. We carried out the screening of mannan-binding type lectin among different species of echinoderms inhabiting in Piter the Grate Bay, the sea of Japan. As a result, the C-type lectins (SJL-32) specific for high mannose glycans was isolated from the coelomic plasma of the sea cucumbers Stichopus japonicus by ion-exchange chromatography on a DEAE-Toyopearl 650M, affinity chromatography on a mannan-Sepharose 6B and gel filtration on a Sephacryl S-200. SJL-32 is homodimer with molecular mass about 32 kDa on SDS-PAGE under non-reducing conditions. Protein part of the lectin has high conteins Asn, Glu, Ser. Hemagglutination of trypsin-treated O blood group human erythrocytes by SJL-32 was competitively inhibited by high-branched -D-mannan composed of -1,2 and -1,6 linked D-mannopyranose residues. In contrast, a variety of mono-, oligo-, and polysaccharides composed of residues of galactose and fucose showed absence or little inhibitory activities. The lectin activity strong depends on Ca2+ concentration, temperature and pH. Monospecific polyclonal antibodies were obtained to the lectin. As was shown by ELISA assay, antibodies to SJL-32 cross-reacted with human serum mannan-binding lectin. This data allows making conclusion about common antigenic determinants and structural homology of both lectins. In our opinion, SJL-32 belongs to evolutionary high conservative mannan-binding lectins (MBLs) family and takes part in the host defense against pathogenic microorganisms.

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면역기능 조절제(MOS, Lectin)와 유기산제(Organic acid F, Organic acid G)가 산란계의 생산성, 혈액성상과 소장내 미생물 균총 및 면역체계에 미치는 영향 (Effects of Supplementary Immune Modulators(MOS, Lectin) and Organic Acid Mixture(Organic acid F, Organic acid G) on the Performance, Profile of Leukocytes and Erythrocytes, Small Intestinal Microflora and Immune Response in Laying Hens)

  • 우경천;김찬호;백인기
    • Journal of Animal Science and Technology
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    • 제49권4호
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    • pp.481-490
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    • 2007
  • 본 시험은 대조구, 항생제 처리구:Avilla- mycin?? 6ppm, MOS 처리구:MOS 250ppm, lectin 처리구:Mannosespepecific lectin 12.5ppm, Organic acid F 처리구:FORMI??(formic acid 35.4%, formate 34.6%, potassium 30.0%) 0.3%, Organic acid G처리구: GALLACID?? 0.06% 등 6처리구를 두고 이들 처리가 산란계에 미치는 영향을 비교 평가하기 위하여 생산성, 혈액성상, 혈청 IgG, 장내 미생물 균총을 조사하였다. 사양시험은 48주령의 산란계(Hy-Line Brown??) 900수를 선별하여 6처리, 5반복, 반복당 15케이지, 케이지당 2수씩 A형 2단 케이지에 수용하고 randomized block design으로 배치하였다. 6주 동안의 산란율(hen-day, hen- house egg production)에서는 MOS 처리구가 가장 높은 산란율을 보였고 모든 첨가구가 대조구보다 산란율이 높았다(P<0.05). 난중은 lectin 처리구가 가장 높았으며 모든 첨가구들이 대조구보다 높은 경향이 있었다. 연파란율은 lectin 처리구를 제외한 모든 첨가구들이 대조구보다 낮았다(P<0.05). 난황색은 Organic acid G 처리구를 제외한 모든 첨가구들이 대조구보다 높았다(P<0.05). Haugh unit는 lectin 처리구가 가장 높았으며 모든 첨가구들이 대조구보다 높았다. Leukocytes 중 SI는 lectin 처리구가 가장 높았다(P<0.05). Erythrocytes 중 RBC, HB, MCHC는 lectin 처리구가 가장 높았으며 MOS 처리구가 가장 낮았다(P<0.05). 장내 미생물에서는 처리구간에 유의적인 차이는 없었으나 Lactobacilli 수는 대조구보다 첨가구들이 높은 경향이 있었고 Cl. perfringens 수는 Organic acid F를 제외한 모든 첨가구들이 대조구보다 낮은 경향이 있었다. 혈청 IgG 농도는 MOS 처리구가 가장 높았으며 모든 첨가구들이 대조구보다 유의적으로 높았다(P<0.05). 결론적으로 본 시험에서 사용된 면역조절제(MOS, Lectin)와 유기산제는 산란계에서 항생제(Avilamycin??)와 유사한 생산성을 나타내어 항생제 대체제로서 산란계의 생산성을 효과적으로 개선 할 수 있으며 특히 이중에서 MOS의 생산성 개선효과가 가장 높았다.

사료내 감태 및 감태로부터 추출한 crude lectin의 첨가가 육계의 생산성 및 면역반응에 미치는 영향

  • 김성권;유선종;안병기;박근규;이훈택;송창선;허억;강창원
    • 한국가금학회:학술대회논문집
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    • 한국가금학회 2004년도 제21차 정기총회 및 학술발표회
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    • pp.23-25
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    • 2004
  • 본 실험은 감태와 crude lectin의 사료내 첨가가육계의 생산성 및 면역반응에 미치는 영향을 조사하기 위하여 실시하였다. 1일령 Ross 수평아리 총234수를 공시하여 대조구(-), 대조구(+), 감태 1.0%, crude lectin 0.05 %, 0.1 %, 및 0.3 %로 6처리 3반복, 반복당 13수씩을 총 38일간 실험사료를 급여하였고, ND-IB 혼합 사독백신은 4일령에 피하접종하였다. 사료요구율에 있어서는 crude lectin 0.3 % 첨가구가 대조구(-)에 비해 유의하게 낮게 나타났다(P<0.05). ND-IB 사독 혼합백신 접종 3주 후에는 감태와 crude lectin의 첨가구의 ND와 IB 백신 역가가 대조구(+)와 비교하여 상승하는 경향이나 상승효과가 있었다(P<0.05). 폐사율에 있어서 crude lectin 첨가구들은 살모넬라를 감염시킨 대조구(+)에 비해 유의하게 감소하였다(P<0.05). 닭에서 IFN-v, IL-2, 및 IL-6의 mRNA는 살모넬라 감염에 의해 높게 발현되었고, 감태와 crude lectin은 IFN-v의 발현에 영향을 미치지 않았으나, 감태 1.0 %와 crude lectin 0.05 % 첨가구는 IL-2와 IL-6의 mRNA 농도가 대조구(+)에 비해 높은 경향이나 유의하게 높았다(p<0.05).

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A Tuber Lectin from Arisaema jacquemontii Blume with Anti-insect and Anti-proliferative Properties

  • Kaur, Manpreet;Singh, Kuljinder;Rup, Pushpinder Jai;Kamboj, Sukhdev Singh;Saxena, Ajit Kumar;Sharma, Madhunika;Bhagat, Madhulika;Sood, Sarvesh Kumar;Singh, Jatinder
    • BMB Reports
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    • 제39권4호
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    • pp.432-440
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    • 2006
  • A tuber lectin from Arisaema jacquemontii Blume belonging to family Araceae was purified by employing a single step affinity chromatography using column of asialofetuin-linked amino activated silica beads and the bound lectin was eluted with 100 mM glycine-HCl buffer pH 2.5. The purified A. jacquemontii lectin (AJL) showed a single protein band with an apparent molecular mass of 13.4 kDa when submitted to SDS-polyacrylamide gel electrophoresis under reducing as well as non-reducing conditions. The native molecular mass of AJL determined by gel filtration on a Biogel P-200 column was 52 kDa and its carbohydrate content was estimated to be 3.40%. Thus AJL is a tetrameric glycoprotein. The purified lectin agglutinated erythrocytes from rabbit but not from human. Its activity was not inhibited by any of the mono- and disaccharides tested except N-acetyl-D-lactosamine having minimal inhibitory sugar concentration (MIC) 25 mM. Among the glycoproteins tested only asialofetuin was found to be inhibitory (MIC $125\;{\mu}g/mL$). A single band was obtained in native PAGE at pH 4.5 while PAGE at pH 8.3 showed two bands. Isoelectric focusing of AJL gave multiple bands in the pI range of 4.6-5.5. When incorporated in artificial diet AJL significantly affected the development of Bactrocera cucurbitae (Coquillett) larvae indicating the possibility of using this lectin in a biotechnological strategy for insect management of cucurbits. Larvae fed on artificial diet containing sub-lethal dose of AJL showed a significant decrease in acid phosphatase and alkaline phosphatase activity while esterase activity markedly increased as compared to larvae fed on diet without lectin. Out of various human cancer cell lines employed in sulphorhodamine B (SRB) assay, this lectin was found to have appreciable inhibitory effect on the in vitro proliferation of HCT-15, HOP-62, SW-620, HT-29, IMR-32, SKOV-3, Colo-205, PC-3, HEP-2 and A-549 cancer cell lines by 82, 77, 73, 70, 41, 41, 37, 29, 21 and 21% respectively.

Thermal Stability of Phaseolus vulgaris Leucoagglutinin: a Differential Scanning Calorimetry Study

  • Biswas, Shyamasri;Kayastha, Arvind M.
    • BMB Reports
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    • 제35권5호
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    • pp.472-475
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    • 2002
  • Phaseolus vulgaris phytohemagglutinin L is a homotetrameric-leucoagglutinating seed lectin. Its three-dimensional structure shows similarity with other members of the legume lectin family. The tetrameric form of this lectin is pH dependent. Gel filtration results showed that the protein exists in its dimeric state at pH 2.5 and as a tetramer at pH 7.2. Contrary to earlier reports on legume lectins that possess canonical dimers, thermal denaturation studies show that the refolding of phytohemagglutinin L at neutral pH is irreversible. Differential scanning calorimetry (DSC) was used to study the denaturation of this lectin as a function of pH that ranged from 2.0 to 3.0. The lectin was found to be extremely thermostable with a transition temperature around $82^{\circ}C$ and above $100^{\circ}C$ at pH 2.5 and 7.2, respectively. The ratio of calorimetric to vant Hoff enthalpy could not be calculated because of its irreversible-folding behavior. However, from the DSC data, it was discovered that the protein remains in its compact-folded state, even at pH 2.3, with the onset of denaturation occurring at $60^{\circ}C$.

Molecular Characterization and Mitogenic Activity of a Lectin from Purse Crab Philyra Pisum

  • Na, Jong-Cheon;Park, Byung-Tae;Chung, Woo-Hyuk;Kim, Ha-Hyung
    • The Korean Journal of Physiology and Pharmacology
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    • 제15권4호
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    • pp.241-244
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    • 2011
  • A lectin from the hemolymph of purse crab, Philyra pisum, was found to have anti-proliferative activity on human lung cancer cells by our laboratory. In this study, P. pisum lectin (PPL) was molecularly characterized including molecular mass, amino acid sequences, amino acid composition, and the effects of metal ions, temperature, and pH on the activity. We found that PPL showed mitogenic activity on human lymphocytes and BALB/c mouse splenocytes. The mitogenic activity (maximum stimulation index, $SI=9.57{\pm}0.59$) of PPL on human lymphocytes was higher than that of a standard well-known plant mitogen, concanavalin A (maximum $SI=8.80{\pm}0.59$). The mitogenic activity mediated by PPL is required for optimum dosing, and higher or lower concentrations caused decreases in mitogenic response. PPL also induced mitogenic activity on mouse splenocytes, however, the maximum SI ($1.77{\pm}0.09$) on mouse splenocytes of PPL was lower than that ($2.14{\pm}0.15$) of concanavalin A. In conclusion, PPL is a metal ion-dependent monomer lectin with mitogenic activity, and could be used as a lymphocyte or splenocyte stimulator.

Loss of Potential Biomarker Proteins Associated with Abundant Proteins during Abundant Protein Removal in Sample Pretreatment

  • Shin, Jihoon;Lee, Jinwook;Cho, Wonryeon
    • Mass Spectrometry Letters
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    • 제9권2호
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    • pp.51-55
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    • 2018
  • Capture of non-glycoproteins during lectin affinity chromatography is frequently observed, although it would seem to be anomalous. In actuality, lectin affinity chromatography works at post-translational modification (PTM) sites on a glycoprotein which is not involved in protein-protein interactions (PPIs). In this study, serial affinity column set (SACS) using lectins followed by proteomics methods was used to identify PPI mechanisms of captured proteins in human plasma. MetaCore, STRING, Ingenuity Pathway Analysis (IPA), and IntAct were individually used to elucidate the interactions of the identified abundant proteins and to obtain the corresponding interaction maps. The abundant non-glycoproteins were captured with the binding to the selected glycoproteins. Therefore, depletion process in sample pretreatment for abundant protein removal should be considered with more caution because it may lose precious disease-related low abundant proteins through PPIs of the removed abundant proteins in human plasma during the depletion process in biomarker discovery. Glycoproteins bearing specific glycans are frequently associated with cancer and can be specifically isolated by lectin affinity chromatography. Therefore, SACS using Lycopersicon esculentum lectin (LEL) can also be used to study disease interactomes.

The Rapid Differentiation of Toxic Alexandrium and Pseudo-nitzschia Species Using Fluorescent Lectin Probes

  • Cho, Eun-Seob;Park, Jong-Gyu;Kim, Hak-Gyoon;Kim, Chang-Hoon;Rhodes, Lesley L.;Chung, Chang-Soo
    • Journal of the korean society of oceanography
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    • 제34권3호
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    • pp.167-171
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    • 1999
  • Since toxic Alexandrium catenella and non-toxic A. fraterculus are morphologically similar, they are difficult to discriminate under the light microscope. However, a novel technology, such as fluorescein isothiocyanate (FITC)-conjugated lectin probes enables easy and rapid differentiation. Toxic A. catenella bound seven different lectins, whereas the non-toxic A. fratercuzus did not bind Arachis hypogaea (PNA) lectin. In addition, Pseudo-nitrschia species in this study were also difficult to identify to species level with light microscope techniques, but it was possible to classify them using fluorescent lectins. Pseudo-nitzschia multistriata, P. subfraudulenta and P. pungens bound Canavalia ensiformis (ConA), whereas P. subpaclfica did not, and P. pungens also bound Ricinus communis (RCA). These results imply that lectin could be used as a critical tool in the differentiation of P. multistriata, P. subfraudulenta and P. pungens. However, P. subpacifica was not differentiated by the lectins tested. Therefore, it isconcluded that lectin probes are useful for discriminating toxic A. catenella from non-toxic A. fraterculus, and for the identification of some Pseudo-nitzschia species. In addition, this method has a great potential to speed and detection between non-toxic and toxic harmful algal blooms (HABs) in Korean biotoxin monitoring systems.

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자유유동 전기이동을 이용한 Lentil Lectin의 분리 (Separation of Lentil Lectin Using Free-Flow Electrophoresis)

  • 류화원;이동일장호남
    • KSBB Journal
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    • 제9권2호
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    • pp.115-121
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    • 1994
  • 240ml의 시료를 정제할 수 있는 30channel의 preparative-scale 자유유동전기이동 분리장치를 제작한 후 렌즈콩으로부터 lentil lectin(LcH)을 전기 집속법으로 분리하였다. 분리된 각 분획을 PAGIEF젤에서 silver staining했을 때 불순물이 전혀 검출되지 않을 정도의 고순도 lectin을 얻을 수 있었다. 이 때 ampholyte로서 HEPES(50mM) -Tris(50mM) -urea(3M) 등을 사용하였으며 50mM Histidine(pI 7.65)인 경우 가장 분리도가 가장 좋았다. LcH는 보통의 조건하에서 LcH-A와 LcH-B의 두가지 순수한 형태로만 나타났으며 따라서 이 장치를 사용하여 다단 분리 정제를 할경우 두 성분의 완전한 분리도 가능함을 보여 주었다.

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