Tsang S K, McDermott B M, Racaniello V R, Hogle J M
Committee on Higher Degrees in Biophysics, Harvard University, Cambridge, Massachusetts 02138, USA.
J Virol. 2001 Jun;75(11):4984-9. doi: 10.1128/JVI.75.11.4984-4989.2001.
We examined the role of soluble poliovirus receptor on the transition of native poliovirus (160S or N particle) to an infectious intermediate (135S or A particle). The viral receptor behaves as a classic transition state theory catalyst, facilitating the N-to-A conversion by lowering the activation energy for the process by 50 kcal/mol. In contrast to earlier studies which demonstrated that capsid-binding drugs inhibit thermally mediated N-to-A conversion through entropic stabilization alone, capsid-binding drugs are shown to inhibit receptor-mediated N-to-A conversion through a combination of enthalpic and entropic effects.
我们研究了可溶性脊髓灰质炎病毒受体在天然脊髓灰质炎病毒(160S或N颗粒)向感染性中间体(135S或A颗粒)转变过程中的作用。病毒受体表现为一种经典的过渡态理论催化剂,通过将该过程的活化能降低50千卡/摩尔来促进N向A的转化。与早期研究表明衣壳结合药物仅通过熵稳定作用抑制热介导的N向A转化不同,本研究表明衣壳结合药物通过焓效应和熵效应的组合来抑制受体介导的N向A转化。