Department of Pathology, University of Maryland School of Medicine, Baltimore, MD, USA.
Cell Biosci. 2012 Sep 12;2(1):32. doi: 10.1186/2045-3701-2-32.
Human Immunodeficiency Virus Type 1 (HIV-1) protease inhibitors (PIs) are the most potent class of drugs in antiretroviral therapies. However, viral drug resistance to PIs could emerge rapidly thus reducing the effectiveness of those drugs. Of note, all current FDA-approved PIs are competitive inhibitors, i.e., inhibitors that compete with substrates for the active enzymatic site. This common inhibitory approach increases the likelihood of developing drug resistant HIV-1 strains that are resistant to many or all current PIs. Hence, new PIs that move away from the current target of the active enzymatic site are needed. Specifically, allosteric inhibitors, inhibitors that prohibit PR enzymatic activities through non-competitive binding to PR, should be sought. Another common feature of current PIs is they were all developed based on the structure-based design. Drugs derived from a structure-based strategy may generate target specific and potent inhibitors. However, this type of drug design can only target one site at a time and drugs discovered by this method are often associated with strong side effects such as cellular toxicity, limiting its number of target choices, efficacy, and applicability. In contrast, a cell-based system may provide a useful alternative strategy that can overcome many of the inherited shortcomings associated with structure-based drug designs. For example, allosteric PIs can be sought using a cell-based system without considering the site or mechanism of inhibition. In addition, a cell-based system can eliminate those PIs that have strong cytotoxic effect. Most importantly, a simple, economical, and easy-to-maintained eukaryotic cellular system such as yeast will allow us to search for potential PIs in a large-scaled high throughput screening (HTS) system, thus increasing the chances of success. Based on our many years of experience in using fission yeast as a model system to study HIV-1 Vpr, we propose the use of fission yeast as a possible surrogate system to study the effects of HIV-1 protease on cellular functions and to explore its utility as a HTS system to search for new PIs to battle HIV-1 resistant strains.
人类免疫缺陷病毒 1 型(HIV-1)蛋白酶抑制剂(PIs)是抗逆转录病毒疗法中最有效的药物类别。然而,病毒对 PIs 的耐药性可能会迅速出现,从而降低这些药物的疗效。值得注意的是,所有当前 FDA 批准的 PIs 都是竞争性抑制剂,即与底物竞争活性酶位的抑制剂。这种常见的抑制方法增加了产生对许多或所有当前 PIs 都耐药的耐药性 HIV-1 株的可能性。因此,需要开发新的不针对当前活性酶位的 PIs。具体来说,应该寻找变构抑制剂,即通过非竞争性结合 PR 来抑制 PR 酶活性的抑制剂。当前 PIs 的另一个共同特征是它们都是基于结构的设计开发的。基于结构的策略产生的药物可能会产生针对特定靶标的有效抑制剂。然而,这种药物设计类型一次只能针对一个靶点,并且通过这种方法发现的药物通常与强烈的副作用(如细胞毒性)相关,限制了其靶点选择、疗效和适用性的数量。相比之下,基于细胞的系统可能提供一种有用的替代策略,可以克服与基于结构的药物设计相关的许多固有缺陷。例如,可以使用基于细胞的系统来寻找变构 PI,而无需考虑抑制的部位或机制。此外,基于细胞的系统可以消除那些具有强烈细胞毒性的 PI。最重要的是,酵母等简单、经济且易于维护的真核细胞系统可以让我们在大规模高通量筛选(HTS)系统中搜索潜在的 PI,从而增加成功的机会。基于我们多年来使用裂殖酵母作为模型系统来研究 HIV-1 Vpr 的经验,我们提出使用裂殖酵母作为研究 HIV-1 蛋白酶对细胞功能影响的替代系统,并探索其作为 HTS 系统的实用性,以寻找新的 PI 来对抗 HIV-1 耐药菌株。