Protein Semi-Synthesis in Living Cells
- 22 May 2003
- journal article
- research article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 125 (24), 7180-7181
- https://doi.org/10.1021/ja034736i
Abstract
Incorporation of chemical probes into proteins is a powerful way to elucidate biological processes and to engineer novel function. Here we describe an approach that allows ligation of synthetic molecules to target proteins in an intracellular environment. A cellular protein is genetically tagged with one-half of a split intein. The complementary half is linked in vitro to the synthetic probe, and this fusion is delivered into cells using a transduction peptide. Association of the intein halves in the cytosol triggers protein trans-splicing, resulting in the ligation of the probe to the target protein through a peptide bond. This process is specific and applicable to cytosolic and integral membrane proteins. The technology should allow cellular proteins to be elaborated with a variety of abiotic probes.Keywords
This publication has 8 references indexed in Scilit:
- A general method for the covalent labeling of fusion proteins with small molecules in vivoNature Biotechnology, 2002
- Protein transduction technologyCurrent Opinion in Biotechnology, 2002
- Unnatural amino acids as probes of protein structure and functionCurrent Opinion in Chemical Biology, 2000
- A Fluorescent Indicator for Detecting Protein−Protein Interactions in Vivo Based on Protein SplicingAnalytical Chemistry, 2000
- Protein Splicing and Related Forms of Protein AutoprocessingAnnual Review of Biochemistry, 2000
- Specific Covalent Labeling of Recombinant Protein Molecules Inside Live CellsScience, 1998
- Segmental Isotope Labeling for Protein NMR Using Peptide SplicingJournal of the American Chemical Society, 1998
- The third helix of the Antennapedia homeodomain translocates through biological membranes.Journal of Biological Chemistry, 1994