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阴离子聚合物的抗HIV-1活性:候选杀微生物剂的比较研究

Anti-HIV-1 activity of anionic polymers: a comparative study of candidate microbicides.

作者信息

Neurath A Robert, Strick Nathan, Li Yun-Yao

机构信息

Biochemical Virology Laboratory, The Lindsley F, Kimball Research Institute of the New York Blood Center, New York, NY 10021, USA.

出版信息

BMC Infect Dis. 2002 Nov 21;2:27. doi: 10.1186/1471-2334-2-27.

Abstract

BACKGROUND

Cellulose acetate phthalate (CAP) in soluble form blocks coreceptor binding sites on the virus envelope glycoprotein gp120 and elicits gp41 six-helix bundle formation, processes involved in virus inactivation. CAP is not soluble at pH < 5.5, normal for microbicide target sites. Therefore, the interaction between insoluble micronized CAP and HIV-1 was studied. Carbomer 974P/BufferGel; carrageenan; cellulose sulfate; dextran/dextrin sulfate, poly(napthalene sulfonate) and poly(styrene-4-sulfonate) are also being considered as anti-HIV-1 microbicides, and their antiviral properties were compared with those of CAP.

METHODS

Enzyme linked immunosorbent assays (ELISA) were used to (1) study HIV-1 IIIB and BaL binding to micronized CAP; (2) detect virus disintegration; and (3) measure gp41 six-helix bundle formation. Cells containing integrated HIV-1 LTR linked to the beta-gal gene and expressing CD4 and coreceptors CXCR4 or CCR5 were used to measure virus infectivity.

RESULTS

  1. HIV-1 IIIB and BaL, respectively, effectively bound to micronized CAP. 2) The interaction between HIV-1 and micronized CAP led to: (a) gp41 six-helix bundle formation; (b) virus disintegration and shedding of envelope glycoproteins; and (c) rapid loss of infectivity. Polymers other than CAP, except Carbomer 974P, elicited gp41 six-helix bundle formation in HIV-1 IIIB but only poly(napthalene sulfonate), in addition to CAP, had this effect on HIV-1 BaL. These polymers differed with respect to their virucidal activities, the differences being more pronounced for HIV-1 BaL.

CONCLUSIONS

Micronized CAP is the only candidate topical microbicide with the capacity to remove rapidly by adsorption from physiological fluids HIV-1 of both the X4 and R5 biotypes and is likely to prevent virus contact with target cells. The interaction between micronized CAP and HIV-1 leads to rapid virus inactivation. Among other anionic polymers, cellulose sulfate, BufferGel and aryl sulfonates appear most effective in this respect.

摘要

背景

可溶形式的邻苯二甲酸醋酸纤维素(CAP)会阻断病毒包膜糖蛋白gp120上的共受体结合位点,并引发gp41六螺旋束的形成,这些过程参与病毒的灭活。CAP在pH值低于5.5时不溶解,而这正是杀微生物剂作用靶点部位的正常pH值。因此,研究了不溶性微粉化CAP与HIV-1之间的相互作用。卡波姆974P/缓冲凝胶、角叉菜胶、硫酸纤维素、葡聚糖/硫酸糊精、聚萘磺酸盐和聚苯乙烯-4-磺酸盐也被视为抗HIV-1杀微生物剂,并将它们的抗病毒特性与CAP的进行了比较。

方法

采用酶联免疫吸附测定(ELISA)来:(1)研究HIV-1 IIIB和BaL与微粉化CAP的结合;(2)检测病毒解体;(3)测定gp41六螺旋束的形成。含有与β-半乳糖苷基因相连的整合型HIV-1长末端重复序列并表达CD4和共受体CXCR4或CCR5的细胞用于测定病毒感染性。

结果

1)HIV-1 IIIB和BaL分别有效地与微粉化CAP结合。2)HIV-1与微粉化CAP之间的相互作用导致:(a)gp41六螺旋束的形成;(b)病毒解体和包膜糖蛋白的脱落;(c)感染性迅速丧失。除卡波姆974P外,CAP以外的聚合物在HIV-1 IIIB中引发了gp41六螺旋束的形成,但除CAP外,只有聚萘磺酸盐对HIV-1 BaL有此作用。这些聚合物在杀病毒活性方面存在差异,对HIV-1 BaL的差异更为明显。

结论

微粉化CAP是唯一一种能够通过吸附从生理流体中快速去除X4和R5两种生物型HIV-1的局部杀微生物剂候选物,并且可能会阻止病毒与靶细胞接触。微粉化CAP与HIV-1之间的相互作用导致病毒迅速失活。在其他阴离子聚合物中,硫酸纤维素、缓冲凝胶和芳基磺酸盐在这方面似乎最有效。

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