Rodrigo Guillermo, Daròs José-Antonio, Elena Santiago F
Instituto de Biología Molecular y Celular de Plantas, Consejo Superior de Investigaciones Científicas - Universidad Politécnica de Valencia, 46022, Valencia, Spain; Instituto de Biología Integrativa y de Sistemas, Consejo Superior de Investigaciones Científicas - Universitat de València, 46980 Paterna, Spain.
Instituto de Biología Molecular y Celular de Plantas, Consejo Superior de Investigaciones Científicas - Universidad Politécnica de Valencia, 46022, Valencia, Spain.
J Proteomics. 2017 Mar 6;156:1-4. doi: 10.1016/j.jprot.2016.12.007. Epub 2016 Dec 20.
Viral infections are extremely complex processes that could only be well understood by precisely characterizing the interaction networks between the virus and the host components. In recent years, much effort has gone in this direction with the aim of unveiling the molecular basis of viral pathology. These networks are mostly formed by viral and host proteins, and are expected to be dynamic both with time and space (i.e., with the progression of infection, as well as with the virus and host genotypes; what we call plastodynamic). This largely overlooked spatio-temporal evolution urgently calls for a change both in the conceptual paradigms and experimental techniques used so far to characterize virus-host interactions. More generally, molecular plasticity and temporal dynamics are unavoidable components of the mechanisms that underlie any complex disease; components whose understanding will eventually enhance our ability to modulate those networks with the aim of improving disease treatments.
病毒感染是极其复杂的过程,只有通过精确表征病毒与宿主成分之间的相互作用网络才能深入理解。近年来,人们朝着这个方向付出了诸多努力,旨在揭示病毒病理学的分子基础。这些网络主要由病毒蛋白和宿主蛋白构成,并且预计会随时间和空间动态变化(即随着感染的进展以及病毒和宿主的基因型而变化;我们称之为可塑性动态变化)。这种在很大程度上被忽视的时空演变迫切要求改变迄今为止用于表征病毒-宿主相互作用的概念范式和实验技术。更普遍地说,分子可塑性和时间动态性是任何复杂疾病潜在机制中不可避免的组成部分;对这些组成部分的理解最终将增强我们调节那些网络以改善疾病治疗的能力。