Interdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh, U.P., India.
Moradabad Institutes of Technology, Moradabad, U.P., India.
Int J Biol Macromol. 2018 Jan;106:1115-1129. doi: 10.1016/j.ijbiomac.2017.07.185. Epub 2017 Sep 8.
This review article summarises the possible mechanisms of the protein-ligand interaction, folding, misfolding, aggregation and inhibition of protein aggregates. Under certain stressed condition the folding process deviates from its path and results into misfolding and aggregation of proteins. So aggregates have to be inhibited in order to cure the diseases. In some cases of protein-ligand interaction studies we have seen that the interaction of a protein with more than one ligand may show both type of quenching mechanisms i.e. dynamic as well as static quenching rather than single type of quenching mechanism, that result can be entirely different by the result of binding study utilising single ligand. So, likewise it is hypothesized that if the aggregates are inhibited by using more than one inhibitor may give more fruitful results rather than application of single inhibitor in inhibition and disaggregation of the preformed aggregates. Therefore, we have hypothesized mechanisms for the inhibition of protein aggregates that may assist in curing the neurodegenerative diseases. Thus, besides the mechanism of protein-ligand interaction, folding, misfolding and aggregation; the hypothesized mechanisms for the inhibition of protein aggregates may show new route to researchers either directly or indirectly in treating the diseases.
这篇综述文章总结了蛋白质-配体相互作用、折叠、错误折叠、聚集和蛋白质聚集物抑制的可能机制。在某些应激条件下,折叠过程偏离其路径,导致蛋白质错误折叠和聚集。因此,为了治疗疾病,必须抑制聚集物。在某些蛋白质-配体相互作用研究中,我们已经看到,一个蛋白质与多个配体的相互作用可能显示两种类型的猝灭机制,即动态和静态猝灭,而不是单一类型的猝灭机制,利用单一配体进行结合研究的结果可能完全不同。因此,同样可以假设,如果使用多种抑制剂来抑制聚集物,可能会比单一抑制剂在抑制和分散已形成的聚集物方面产生更有成效的结果。因此,我们提出了抑制蛋白质聚集物的机制,这可能有助于治疗神经退行性疾病。因此,除了蛋白质-配体相互作用、折叠、错误折叠和聚集的机制外,抑制蛋白质聚集物的假设机制可能为研究人员在治疗疾病方面提供新的途径,无论是直接的还是间接的。