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Protein manipulation using single copies of short peptide tags in cultured cells and in . | LitMetric

AI Article Synopsis

  • Cellular development depends on dynamic protein interactions, which are key topics in research on cell processes like migration and division.
  • Traditional methods have focused on genetic manipulation of proteins of interest (POIs), but there is a need for more direct control over these interactions.
  • Recent advancements in synthetic biology have led to the creation of specific protein binders that can effectively target and manipulate POIs in living cells using short-tag epitopes.

Article Abstract

Cellular development and function rely on highly dynamic molecular interactions among proteins distributed in all cell compartments. Analysis of these interactions has been one of the main topics in cellular and developmental research, and has been mostly achieved by the manipulation of proteins of interest (POIs) at the genetic level. Although genetic strategies have significantly contributed to our current understanding, targeting specific interactions of POIs in a time- and space-controlled manner or analysing the role of POIs in dynamic cellular processes, such as cell migration or cell division, would benefit from more-direct approaches. The recent development of specific protein binders, which can be expressed and function intracellularly, along with advancement in synthetic biology, have contributed to the creation of a new toolbox for direct protein manipulations. Here, we have selected a number of short-tag epitopes for which protein binders from different scaffolds have been generated and showed that single copies of these tags allowed efficient POI binding and manipulation in living cells. Using , we also find that single short tags can be used for POI manipulation .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7990863PMC
http://dx.doi.org/10.1242/dev.191700DOI Listing

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