Product Name:ZIP (Scrambled)
CAS No:908012-18-0
Purity:95%
Molar Mass:1928.4
Chemical Formula:C90H154N30O17
Storage:Store at -20 degrees Celsius
Sequence:RLYRKRIWRSAGR
Application:
ZIP (Scrambled) is a control peptide used in research studies to investigate the specificity of the ??-inhibitory peptide (ZIP), which targets protein kinase M?? (PKM??), a key enzyme involved in memory formation and synaptic plasticity. ZIP (Scrambled) has a randomized sequence compared to the active ZIP peptide, rendering it inactive while retaining similar molecular properties. It is primarily used as a negative control to ensure that any observed biological effects are specific to the ZIP sequence. This peptide is widely utilized in neurobiology and cognitive research, particularly in studies related to memory and learning.
Current Research:
Zeta inhibitory peptide (ZIP), with the CAS number 863987-12-6, is a synthetic, cell-permeable peptide that functions as a selective inhibitor of protein kinase M?? (PKM??), an atypical isoform of protein kinase C (PKC). PKM?? is implicated in the maintenance of long-term potentiation (LTP), a cellular mechanism underlying learning and memory. ZIP has been instrumental in elucidating the role of PKM?? in synaptic plasticity and memory processes.
The peptide sequence of ZIP is Myr-Ser-Ile-Tyr-Arg-Arg-Gly-Ala-Arg-Arg-Trp-Arg-Lys-Leu-OH, where "Myr" denotes an N-terminal myristoylation, enhancing its membrane permeability. By mimicking the pseudosubstrate region of PKM??, ZIP effectively inhibits its kinase activity.
In vitro studies have demonstrated that ZIP can reverse late-phase LTP in hippocampal slices, with an IC?? ranging from 1 to 2.5 ??M. In vivo, central administration of ZIP has been shown to disrupt established spatial memory, indicating its potential to interfere with memory maintenance. These findings have positioned ZIP as a critical tool in neuroscience research, particularly in studies investigating the molecular underpinnings of memory storage and persistence.
However, the specificity of ZIP has been a subject of debate. Some studies suggest that its effects may not be exclusively mediated through PKM?? inhibition, as ZIP has been observed to influence other signaling pathways, including those involving ionotropic glutamate receptors. This has led to discussions regarding the interpretation of experimental outcomes where ZIP is utilized, emphasizing the necessity for cautious analysis of its effects.
In summary, ZIP serves as a potent inhibitor of PKM??, offering valuable insights into the molecular mechanisms of synaptic plasticity and memory. Nonetheless, its broader impact on various signaling pathways necessitates careful consideration in experimental designs and data interpretation.
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