Cosic Irena, Cosic Drasko, Lazar Katarina
RMIT University, La Trobe Street, Melbourne, VIC, 3000, Australia.
AMALNA Consulting, 46 Second St, Black Rock, VIC, 3193, Australia.
Cell Biochem Biophys. 2016 Jun;74(2):175-80. doi: 10.1007/s12013-015-0716-3.
The tumor necrosis factor (TNF) is a complex protein that plays a very important role in a number of biological functions including apoptotic cell death, tumor regression, cachexia, inflammation inhibition of tumorigenesis and viral replication. Its most interesting function is that it is an inhibitor of tumorigenesis and inductor of apoptosis. Thus, the TNF could be a good candidate for cancer therapy. However, the TNF has also inflammatory and toxic effects. Therefore, it would be very important to understand complex functions of the TNF and consequently be able to predict mutations or even design the new TNF-related proteins that will have only a tumor inhibition function, but not other side effects. This can be achieved by applying the resonant recognition model (RRM), a unique computational model of analysing macromolecular sequences of proteins, DNA and RNA. The RRM is based on finding that certain periodicities in distribution of free electron energies along protein, DNA and RNA are strongly correlated to the biological function of these macromolecules. Thus, based on these findings, the RRM has capabilities of protein function identification, prediction of bioactive amino acids and protein design with desired biological function. Using the RRM, we separate different functions of TNF as different periodicities (frequencies) within the distribution of free energy electrons along TNF protein. Interestingly, these characteristic TNF frequencies are related to previously identified characteristics of proto-oncogene and oncogene proteins describing TNF involvement in oncogenesis. Consequently, we identify the key amino acids related to the crucial TNF function, i.e. receptor recognition. We have also designed the peptide which will have the ability to recognise the receptor without side effects.
肿瘤坏死因子(TNF)是一种复杂的蛋白质,在许多生物学功能中发挥着非常重要的作用,包括凋亡性细胞死亡、肿瘤消退、恶病质、炎症、肿瘤发生抑制和病毒复制。其最有趣的功能是它是肿瘤发生的抑制剂和凋亡诱导剂。因此,TNF可能是癌症治疗的良好候选物。然而,TNF也具有炎症和毒性作用。因此,了解TNF的复杂功能并进而能够预测突变,甚至设计出仅具有肿瘤抑制功能而无其他副作用的新型TNF相关蛋白质将非常重要。这可以通过应用共振识别模型(RRM)来实现,RRM是一种分析蛋白质、DNA和RNA大分子序列的独特计算模型。RRM基于这样的发现:沿蛋白质、DNA和RNA的自由电子能量分布中的某些周期性与这些大分子的生物学功能密切相关。因此,基于这些发现,RRM具有蛋白质功能识别、生物活性氨基酸预测以及设计具有所需生物学功能的蛋白质的能力。利用RRM,我们将TNF的不同功能分离为沿TNF蛋白质的自由能电子分布内的不同周期性(频率)。有趣的是,这些特征性的TNF频率与先前确定的原癌基因和癌基因蛋白质的特征相关,这些特征描述了TNF在肿瘤发生中的作用。因此,我们确定了与TNF关键功能即受体识别相关的关键氨基酸。我们还设计了一种能够识别受体且无副作用的肽。