کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
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1378673 | 982006 | 2006 | 5 صفحه PDF | دانلود رایگان |

Tylophorine B exhibits 60% inhibition against tobacco mosaic virus (TMV) at a concentration of 1.0 × 10−6 g/ml. In our study, high affinity for TMV RNA and assembly origin of TMV RNA (oriRNA) was revealed, accompanied by the conformational change of RNA. Considering that TMV assembly begins with the specific recognition by the coat protein aggregate of oriRNA, and that tylophorine B has favorable interaction with oriRNA, we speculate that tylophorine B likely exerts its virus inhibition by binding to oriRNA and interfering with virus assembly initiation. This work may shed light on the possible molecular inhibition mechanism against TMV by tylophorine B, and provide clues in rational design of sequence-specific RNA binding antivirus drugs.
Tobacco mosaic virus (TMV) inhibitor tylophorine B binds to TMV RNA in multiple binding sites with IC50 of 2.4 nM. It also binds to assembly origin of TMV RNA with one binding site of Kd of 9 nM. We speculate that tylophorine B likely exerts its virus inhibition by binding to assembly origin, and interfering with virus assembly initiation.Figure optionsDownload as PowerPoint slide
Journal: Bioorganic & Medicinal Chemistry Letters - Volume 16, Issue 16, 15 August 2006, Pages 4300–4304