Intermolelular communication between a receptor incorporated into liposome and lactate dehydrogenase(LDH) adsorbed on the membrane was established on artificial membranes,mediated by Cu2+.The receptor,having a moiety ...Intermolelular communication between a receptor incorporated into liposome and lactate dehydrogenase(LDH) adsorbed on the membrane was established on artificial membranes,mediated by Cu2+.The receptor,having a moiety of pseudo-crown ether binding K+ and two histidine residues binding Cu2+,is a gemini compound with heteroditopic ion recognition site of Cu2+ as an inhibitor of the enzyme and K+ as a stimulating signal.The relative activity of the enzyme was 40.9% due to the inhibition of Cu2+ in the absence of K +,up to 85.9% in the presence of K +.In the communication system,the K+ signal was transduced to LDH by the receptor,leading to enhancement of LDH activity.展开更多
研究红景天苷(Salidroside,SAL)对乳腺癌尤其是三阴性乳腺癌(triple negative breast cancer,TNBC)细胞增殖的影响,探讨其作用机制。应用不同浓度的SAL处理TNBC和非TNBC细胞,计算细胞增殖率和不同乳腺癌细胞的IC50,寻找SAL的最佳浓度。...研究红景天苷(Salidroside,SAL)对乳腺癌尤其是三阴性乳腺癌(triple negative breast cancer,TNBC)细胞增殖的影响,探讨其作用机制。应用不同浓度的SAL处理TNBC和非TNBC细胞,计算细胞增殖率和不同乳腺癌细胞的IC50,寻找SAL的最佳浓度。划痕实验检测SAL对MDA-MB-231细胞迁移的影响。qPCR检测SAL处理后乳腺癌细胞Bcl-2的表达。应用Target Scan预测作用于Bcl-2的miRNA,荧光素酶实验验证miRNA与Bcl-2的靶向关系。展开更多
文摘Intermolelular communication between a receptor incorporated into liposome and lactate dehydrogenase(LDH) adsorbed on the membrane was established on artificial membranes,mediated by Cu2+.The receptor,having a moiety of pseudo-crown ether binding K+ and two histidine residues binding Cu2+,is a gemini compound with heteroditopic ion recognition site of Cu2+ as an inhibitor of the enzyme and K+ as a stimulating signal.The relative activity of the enzyme was 40.9% due to the inhibition of Cu2+ in the absence of K +,up to 85.9% in the presence of K +.In the communication system,the K+ signal was transduced to LDH by the receptor,leading to enhancement of LDH activity.
文摘研究红景天苷(Salidroside,SAL)对乳腺癌尤其是三阴性乳腺癌(triple negative breast cancer,TNBC)细胞增殖的影响,探讨其作用机制。应用不同浓度的SAL处理TNBC和非TNBC细胞,计算细胞增殖率和不同乳腺癌细胞的IC50,寻找SAL的最佳浓度。划痕实验检测SAL对MDA-MB-231细胞迁移的影响。qPCR检测SAL处理后乳腺癌细胞Bcl-2的表达。应用Target Scan预测作用于Bcl-2的miRNA,荧光素酶实验验证miRNA与Bcl-2的靶向关系。