Influenza B neuraminidase (NA) is a critical component in the viral life cycle, facilitating the release of progeny virions from infected cells. While the interest generally veers towards inhibiting its activity, understanding activators, even if indirect, provides a broader insight into its regulation. Essential minerals like Zinc, present as Zinc sulfate, and Manganese, provided as Manganese(II) sulfate, are known to aid a myriad of enzymatic functions. They can ensure the proper folding, stabilization, and activity of proteins, including viral proteins like NA. Moreover, energy substrates such as Pyruvate and D-glucose play pivotal roles in cellular respiration and energy production. Boosting cellular ATP levels indirectly shores up the energy-intensive processes associated with viral replication, providing an environment where NA can function optimally. Similarly, compounds like Caffeine and Epinephrine that enhance the cellular metabolic rate or intracellular signaling can set the stage for heightened cellular activities, which might indirectly bolster the operations of NA.
Certain compounds influence the cellular state or its resilience. For instance, Retinoic acid, which governs gene expression and cellular differentiation, can create a differential cellular state. Such states might offer a backdrop where NA's expression and functionality are indirectly modulated. Meanwhile, Vitamin E, with its antioxidant capacities, shields cells from oxidative damages. By preserving cellular integrity, it ensures a conducive environment for proteins like NA to maintain their structure and function. Another aspect to consider is the direct impact on protein structures and functions. Molecules like Cysteine play a role in ensuring the structural integrity of proteins. By aiding in the formation of disulfide bonds, they ensure that proteins, possibly including NA, attain and retain their native conformations essential for their function. On the whole, the regulatory landscape of Influenza B NA, while majorly geared towards inhibition, has facets where indirect activation is possible. Delving into these facets offers a comprehensive understanding of this pivotal viral protein.
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