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[1,2,6-三-O-没食子酰基-β-D-吡喃葡萄糖抑制gp41介导的HIV包膜与靶细胞膜融合]

[1,2,6-tri-O-galloyl-beta-D-glucopyranose inhibits gp41-mediated HIV envelope fusion with target cell membrane].

作者信息

Sun Wei, Wang Hong-tao, Xia Cheng-lai, Wu Shu-guang, Jiang Shi-bo, Jiang Zhi-hong, Liu Shu-wen

机构信息

School of Pharmaceutical Science, Southern Medical University, Guangzhou 510515, China.

出版信息

Nan Fang Yi Ke Da Xue Xue Bao. 2008 Jul;28(7):1127-31.

Abstract

OBJECTIVE

To observe the inhibitory effect of 1,2,6-Tri-O-galloyl-beta-D-glucopyranose (TGGP) from Balanophora japonica Makino on human immunodeficiency virus (HIV) entry into the host cells and explore the mechanisms.

METHODS

TGGP was purified from Balanophora japonica Makino by n-hexane and ethyl acetate extraction and column chromatography. The inhibitory activity of TGGP on HIV gp41 six-helix bundle formation was measured with ELISA, N-PAGE and SE-HPLC, and the inhibitory effect of TGGP on HIV envelope grlycoprotein-induced cell-cell fusion was detected using a non-infectious cell-based assay.

RESULTS

TGGP inhibited HIV gp41 six-helix bundle formation, with an IC50 of 1.37-/+0.19 microg/ml as determined by ELISA, and this activity was further confirmed by N-PAGE and SE-HPLC. TGGP at 25 microg/ml significantly inhibited syncytium formation between the effector (CHO-WT) and the target (MT-2) cells.

CONCLUSION

The HIV transmembrane subunit gp41 mediates the entry of HIV into the target cells. TGGP can inhibit HIV fusion and entry into the target cells by inhibiting the formation of gp41 six-helix bundles, suggesting the potential of TGGP as a microbicide to prevent sexual transmission of HIV.

摘要

目的

观察日本蛇菰中1,2,6-三-O-没食子酰基-β-D-吡喃葡萄糖(TGGP)对人免疫缺陷病毒(HIV)进入宿主细胞的抑制作用并探讨其机制。

方法

通过正己烷和乙酸乙酯萃取及柱色谱法从日本蛇菰中纯化TGGP。采用ELISA、N-PAGE和SE-HPLC检测TGGP对HIV gp41六螺旋束形成的抑制活性,使用基于非感染性细胞的检测方法检测TGGP对HIV包膜糖蛋白诱导的细胞-细胞融合的抑制作用。

结果

TGGP抑制HIV gp41六螺旋束形成,ELISA测定其IC50为1.37±0.19μg/ml,N-PAGE和SE-HPLC进一步证实了该活性。25μg/ml的TGGP显著抑制效应细胞(CHO-WT)与靶细胞(MT-2)之间的合胞体形成。

结论

HIV跨膜亚基gp41介导HIV进入靶细胞。TGGP可通过抑制gp41六螺旋束的形成来抑制HIV融合及进入靶细胞,提示TGGP作为预防HIV性传播的杀微生物剂的潜力。

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