AI Article Synopsis

  • Intein-mediated protein ligation (IPL) uses an intein to create proteins with a C-terminal thioester, enabling attachment to other proteins or peptides with an amino-terminal cysteine.
  • This method allows for isolation and labeling of recombinant proteins in E. coli by using synthetic short peptides containing a fluorescent group.
  • The chapter further discusses important factors influencing intein-mediated cleavage and ligation processes.

Article Abstract

Intein-mediated protein ligation (IPL) employs an intein to create a protein possessing a C-terminal thioester that can be ligated to a protein or peptide with an amino-terminal cysteine via a native peptide bond. Here we present a procedure to conduct isolation and labeling of recombinant proteins expressed in E. coli using synthetic short peptides possessing a fluorescent moiety. This approach can be readily utilized for site-specific conjugation of a fluorophore to the C-terminus of a protein of interest, without the drawback of non-specific chemical labeling. This chapter also gives a general review of the critical parameters of intein-mediated cleavage and ligation reactions.

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Source
http://dx.doi.org/10.1007/978-1-61737-967-3_6DOI Listing

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