• Journal of Yeungnam Medical Science
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• 제4권1호
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• pp.17-23
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• 1987

백서심장조직을 trypsin과 collagenase 두가지의 효소를 사용하여 분리하면서 각 효소의 분리효과와 두가지 효소의 복합적 세포분리효과를 조사하였으며 이와 동시에 dimethyl sulfoxide가 세포분리과정 및 단기간 배양중에 세포에 미치는 효과를 조사한 결과를 다음과 같이 요약할 수 있다. 1. 백서심장조직에서 세포를 분리할 때 $4^{\circ}C$ trypsin 18시간 전처치후 $37^{\circ}C$ collagenase 처치한 군에서 세포생존율 세포수확량 및 심근세포 생존율이 가장 높았다. 즉 단일 효소 처리보다는 효소 복합연속 처리가 더 효율적이었다. 2. $37^{\circ}C$ trypsin만으로 세포분리를 하였을 때 세포생존율과 수확량이 가장 낮았다. 3. 백서심장세포의 분리과정과 초기 배양 과정에 세포회복이나 보호에 대한 DMSO의 효과는 인정되지 않았으며 오히려 세포파괴 효과가 높음을 알 수 있었다.

• Journal of Periodontal and Implant Science
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• 제23권3호
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• pp.442-453
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• 1993

In order to determine the relationship between probing pocket depth and trypsin-like activity in subgingival plaque, probing pocket depth and loss of attachment were measured by Michigan-O probe on mandibular incisors of 30 patients with adult periodontitis. And the trypsin-like activity of Treponema denticola, Porphyromonas gingivalis, and Bacteroides forsythus was evaluated by the hydrolysis of N-Benzoyl-DL-Arginine-2-Naphthyla-mide (BANA) using PerioScan reagent cards(Oral-B Laboratories, Redwood City, CA). The obtained data were statistically analyzed by Microstat program. The results were as follows. 1. The number of teeth showing negative trypsin-like activity was more in shallow periodontal pocket groups, but the number of teeth showing positive trypsin-like activity was more in deep periodontal pocket groups. 2. There was a significant positive correlation between probing pocket depth and trypsin-like activity in subgingival plaque(y=0.413X - 0.955, r = 0.7024, p<0.001). 3. There was no consistent relationship between loss of attachment and trypsin-like activity in subgingival plaque(p>0.01).

• Archives of Pharmacal Research
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• 제27권11호
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• pp.1141-1146
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• 2004

Lonicera japonica Thunb.(Caprifoliaceae) has long been known as an anti-inflammatory. In the present study, the effect of water fraction of Lonicera japonica (LJ) on trypsin-induced mast cell activation was examined. HMC-1 cells were stimulated with trypsin (100 nM) in the presence or absence of LJ (10, 100, and 1000 $\mu$ g/mL). TNF-$\alpha$ and tryptase production were measured by enzyme-linked immunosorbent assay (ELISA) and reverse transcription-PCR. Extracellular signal-regulated kinase (ERK) phosphorylation was assessed by Western blot. Trypsin activity was measured by using Bz-DL-Arg-p-nitroanilide (BAPNA) as substrate. LJ (10, 100, and 1000 $\mu$g/mL) inhibited TNF-$\alpha$ secretion in a dose-dependent manner. LJ (10, 100, and 1000 $\mu$g/mL) also inhibited TNF-$\alpha$ and tryptase mRNA expression in trypsin-stimulated HMC-1. Furthermore, LJ inhibited trypsin-induced ERK phosphorylation. However, LJ did not affect the trypsin activity even 1000 $\mu$g/mL. These results indicate that LJ may inhibit trypsin-induced mast cell activation through the inhibition of ERK phosphorylation than the inhibition of trypsin activity.

• Journal of Ginseng Research
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• 제28권3호
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• pp.127-131
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• 2004

홍삼 물 추출물이 효소활성에 미치는 영향을 조사하기 위하여 먼저 홍삼분말에 methyl alcohol을 가하여 지용성 성분과 사포닌 성분을 추출하여 제거하였다. 그 잔사에 정제수를 가하여 추출한 뒤 추출물을 제조하였고, 투석막을 이용하여 분자량 크기별로 분획한 뒤 trypsin의 활성에 미치는 영향을 조사하였다. 몇 가지 분획 중에서 분자량 1,000∼12,000 사이의 분획이 trypsin 활성을 가장 강하게 증가시켰다. 분자량 1,000∼12,000 사이의 분획을 여러 가지 농도별로 첨가하여 trypsin 활성에 미치는 영향을 조사한 결과 2.9${\times}$$10^{-3}$%에서 15% 정도 촉진되었으며, 농도가 높아질수록 trypsin 활성도 증가하여 9${\times}$$10^{-2}$%에서 최고의 활성을 보이다가 그 이상의 농도에서는 감소하였다. Trypsin의 casein 분해에 있어서 물 추출물은 Km 값을 낮게하고 Vmax 값은 증가기켰다. 물 추출물을 부분 정제하여 몇 가지 특성을 조사한 겨로가 ninhydrin, DNS 및 Folin시약에 양성반응을 나타내는 것으로 보아 함질소 화합물이라고 판단된다.

• 한국식품과학회지
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• 제26권1호
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• pp.81-87
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• 1994

하늘타리박의 뿌리인 괄루근에서 분리 정제한 trypsin inhibitor는 TRTI-1과 TRTI-2 두 종류였으며 gel-filtration과 SDS-PAGE 전기영동에서 얻은 결과로부터 TRTI-1은 $4,000{\sim}5,000\;Da$의 분자량을 가진 monomer이며 TRTI-2는 $20,000{\sim}24,000\;Da$의 분자량을 가친 homodimer임을 알 수 있었다. 온도의 안정성에 있어서는 TRTI-1은 $100^{\circ}C$에서 2시간 이상 안정하였으며, TRTI-2는 $0{\sim}70^{\circ}C$의 온도에서는 안정하였으나 $80^{\circ}C$에서부터는 안정성이 떨어지면서 $100^{\circ}C$에서는 저해능이 완전히 소실되었다. Trypsin 활성에 대해서 TRTI-1, TRTI-2 및 상품화된 soybean BBI의 농도에 따른 저해능을 보면 TRTI-1, TRTI-2 및 soybean BBI의 각각의 농도가 $0.8{\mu}M,\;6{\mu}M,\;4{\mu}M$일 때 1mg/ml의 trypsin을 50% 저해하였으며, trypsin의 반응속도에 대한 TRTI의 저해 실험에서 TRTI-1와 TRTI-2 모두 trypsin의 가수분해를 경쟁적으로 저해하였으며 $K_{m}$값은 저해제가 없는 경우 $0.37\;{\mu}M$에 대해 각각 0.97, $0.63\;{\mu}M$이었다. 여러 protease에 대한 TRTI-1과 TRTI-2의 저해능 실험 결과 elastase, pepsin, Nagarase, papain, thermolysin, chymotrypsin, thrombin 및 collagenase 등은 저해하지 못하였고 trypsin만을 특이하게 저해하였다.

• IMMUNE NETWORK
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• 제5권4호
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• pp.193-198
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• 2005

Background: Protease-activated receptor 2 (PAR2) belongs to a family of G protein coupled receptors activated by proteolytic cleavage. Trypsin-like serine proteases interact with PAR2 expressed by a variety of tissues and immune cells. The aim of our study was to investigate whether PAR2 stimulation can lead to the activation of human mac rophages. Methods: PAR2-mediated proliferation of human macrophage cell line THP-1 was measured with MTT assay. We also examined the extracellular regulated kinase (ERK) phosphorylation and cytokine production induced by trypsin and PAR2-agonist using western blot and enzyme-linked immunosorbent assay (ELISA), respectively. Results: Treatment of trypsin or PAR2-activating peptide increased cell proliferation in a dose-dependent manner, and induced the activation of ERK1/2 in THP-1 cells. In addition, trypsin-induced cell proliferation was inhibited by pretreatment of an ERK inhibitor (pD98059) or trypsin inhibitor (SBTI). Moreover, PAR2 activation by trypsin increased the secretion of TNF-${\alpha}$ in THP-1 cells. Conclusion: There results suggest that P AR2 activation by trypsin-like serine proteases can induce cell proliferation through the activation of ERK in human macrophage and that PAR2 may playa crucial role in the cell proliferation and cytokine secretion induced by trypsin-like serine proteases.

• 약학회지
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• 제49권5호
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• pp.410-415
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• 2005

To investigate biological activity of noni extracts treated with HCl and trypsin, we measured the antioxidant activity through vitro assay and cellular system. Both water and lipid soluble fraction of noni extracts dose-dependently scav­enged DPPH radical. Superoxide scavenging activity of lipid soluble fraction after treating HCl and trypsin was significantly more potent than those of other fractions in NBT/xanthine oxidase assay, which suggests that antioxidant activity of noni extracts was increased by the treatment with HCl and trypsin. In antioxidant assay using RBL 2H3 cells, water soluble frac­tion of noni extracts had little effect on silica-induced reactive oxygen species generation, whereas lipid soluble fraction inhibited in a dose dependent manner. In non-treated noni extracts, effect of water soluble fraction on silica/$CuSO_4$-induced lipid peroxidation was more potent than that of lipid soluble fraction. However, the effects of noni extracts were reversed in noni extracts treated with HCl and trypsin. These data suggest that water soluble substances may be converted into lipid soluble substances by the treatment with HCl and trypsin. From the above results, it is suggested that lipid soluble fraction of noni extracts contain antioxidant used in vitro assay and RBL 2H3 cellular system. Such an effect of noni extracts may be increased by the treatment with HCl and trypsin.

• Fisheries and Aquatic Sciences
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• 제1권2호
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• pp.209-215
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• 1998

Trypsin-like enzyme was purified from shrimp hepatopancreas through Q-Sepharose ionic exchange, benzamidine Sepharose-6B affinity, and Superdex 75 gel chromatography. Purity of trypsin-like enzyme was increased 69-fold with $44\%$ yield. The enzyme consisted of a single polypeptide chain with a molecular weight (M.W.) of 32 kDa judged by sodium dodecylsulfate polyacrylamide gel electrophoresis (SDS-PAGE). The enzyme was completely inactivated by serine enzyme inhibitors such as soybean trypsin inhibitor (SBTI), tosyl-L­lysine chloromethyl ketone (TLCK), and leupeptin. However, the enzyme was not affected by tosyl-L-phenylalanine chloromethyl ketone (TPCK) which is a chymotrypsin specific inhibitor. The enzyme had no activity against benzoyl-tyrosine ethyl ester (BTEE) which is a chymotrypsin specific substrate. The enzyme showed high activity on the carboxyl terminal of Phe, Tyr. Glu, Arg, and Asp. However. no activity was detected against the carboxyl terminal of Pro, Trp, Cys, Gly, Val, and Ala.

• Natural Product Sciences
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• 제13권2호
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• pp.169-173
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• 2007

Luteolin is a major flavonoid of Lonicera japonica and has anti-inflammatory effect. The activation of proteinase-activated receptor (PAR)-2 and -4 by trypsin appears to play a role in inflammation, In the present study, we examined the inhibitory effects of luteolin on activation of trypsin-induced human leukemic mast cells (HMC-1). HMC-1 cells were stimulated with trypsin, PAR-2 and PAR-4 agonist, in the presence or absence of luteolin. The level of TNF-${\alpha}$ secretion was measured by enzyme-linked immunosorbent assay (ELISA). The expression of tryptase and phosphorylated-extracellular signal-regulated kinase (ERK) were assessed by Westem blot analysis. Moreover, trypsin activity was measured by the substrate Bz-DL-Arg-p-nitroanilide (BAPNA). TNF-${\alpha}$ secretion and Tryptase expression in trypsin-stimulated HMC-1 cells were markedly inhibited by pretreatment of luteolin. Furthermore, the pretreatment of luteolin resulted in the reduction of ERK phosphorylation and trypsin activity. These results suggest that luteolin might has the inhibitory effects on the PAR-2 and -4-dependent inflammation.

• 한국양식학회지
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• 제18권4호
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• pp.245-251
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• 2005

본 연구는 rotifer, B. rotundiformis를 대상으로 소화효소 실험을 하기 위해 이들이 가지고 있는 소화효소의 최고 활성 조건을 확인하기 위해 수행하였다. rotifer, B. rotundiformis의 $\alpha$-amylase, total alkaline Protease, trypsin 및 TG-lipase는 Tris-HCl buffer 보다 phosphate-NaOH buffer 안정적인 효소활성을 보였다. $\alpha$-amylase, trypsin 및 TG-lipase는 pH 8.0에서, total alkaline proteaset pH 7.0에서 높은 효소 활성을 나타내었다. $\alpha$-amylase 활성은 $40^{\circ}C$에서 가장 높은 활성을 보였으며, total alkaline pretense와 trypsin은 $55{\~}60^{\circ}C$의 온도에서 높은 활성을 나타내었다. 반면 TG-lipase 활성은 $25{\~}30^{\circ}C$의 낮은 온도에서 활성이 높았다. $\alpha$-amylase, total alkaline pretense, trypsin 및 TG-lipase의 활성의 적정 기질 농도는 $3.5\%$ starch, $\0.6%$ azo-casein, $87.5{\mu}M$ BApNA and 81.2 mM olive oil이었다. $\alpha$-amylase, total alkaline protease, trypsin 및 TG-lipase의 활성의 적정 반응시간은 40, 60, 30 and 25 min으로 나타났다. 본 연구 결과에서 얻어진 자료는 rotifer, B. rotundiformis의 소화효소 연구를 위한 기초 자료로 이용될 것이다.