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Isolation and Characterization of a Phaseolus vulgaris Trypsin Inhibitor with Antiproliferative Activity on Leukemia and Lymphoma Cells

机译:具有对白血病和淋巴瘤细胞抗增殖活性的菜豆胰蛋白酶抑制剂的分离与鉴定

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摘要

A 17.5-kDa trypsin inhibitor was purified from Phaseolus vulgaris cv. “gold bean” with an isolation protocol including ion exchange chromatography on DEAE-cellulose (Diethylaminoethyl-cellulose), affinity chromatography on Affi-gel blue gel, ion exchange chromatography on SP-sepharose (Sulfopropyl-sepharose), and gel filtration by FPLC (Fast protein liquid chromatography) on Superdex 75. It dose-dependently inhibited trypsin with an IC50 value of 0.4 μM, and this activity was reduced in the presence of dithiothreitol in a dose- and time-dependent manner, signifying the importance of the disulfide linkage to the activity. It inhibited [methyl-3H] thymidine incorporation by leukemia L1210 cells and lymphoma MBL2 cells with an IC50 value of 2.3 μM and 2.5 μM, respectively. The inhibitor had no effect on fungal growth and the activities of various viral enzymes when tested up to 100 μM.
机译:从菜豆中提取17.5kDa的胰蛋白酶抑制剂。具有分离方案的“金豆”,包括在DEAE-纤维素上的离子交换色谱(二乙基氨基乙基纤维素),在Affi-凝胶蓝胶上的亲和色谱,在SP-琼脂糖上的离子交换色谱(磺丙基-琼脂糖)和通过FPLC进行凝胶过滤(快速蛋白液相色谱)在Superdex 75上。它以剂量依赖性地抑制胰蛋白酶,IC50值为0.4μM,在二硫苏糖醇存在下,该活性以剂量和时间依赖性方式降低,表明了二硫键的重要性参加活动。它抑制白血病L1210细胞和淋巴瘤MBL2细胞的[methyl- 3 H]胸苷掺入,IC50值分别为2.3μM和2.5μM。当测试至100μM时,该抑制剂对真菌生长和各种病毒酶的活性没有影响。

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