Home LiteratureArticle Details
PMID: 9618476 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Expressed protein ligation: a general method for protein engineering.

Muir TW, Sondhi D, Cole PA

Abstract

A protein semisynthesis method-expressed protein ligation-is described that involves the chemoselective addition of a peptide to a recombinant protein. This method was used to ligate a phosphotyrosine peptide to the C terminus of the protein tyrosine kinase C-terminal Src kinase (Csk). By intercepting a thioester generated in the recombinant protein with an N-terminal cysteine containing synthetic peptide, near quantitative chemical ligation of the peptide to the protein was achieved. The semisynthetic tail-phosphorylated Csk showed evidence of an intramolecular phosphotyrosine-Src homology 2 interaction and an unexpected increase in catalytic phosphoryl transfer efficiency toward a physiologically relevant substrate compared with the non-tail-phosphorylated control. This work illustrates that expressed protein ligation is a simple and powerful new method in protein engineering to introduce sequences of unnatural amino acids, posttranslational modifications, and biophysical probes into proteins of any size.

MeSH Terms
Animals Humans Protein Engineering/methods Proteins/chemistry,genetics Recombinant Proteins/chemistry,genetics
Chemicals
Proteins Recombinant Proteins
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Muir T W
Laboratory of Synthetic Protein Chemistry, Rockefeller University, 1230 York Avenue, New York, NY 10021, USA. muirt@rockvax.rockefeller.edu
Sondhi D
Cole P A
References (26)
26 references, click to expand
  1. Cloning of a complementary DNA for a protein-tyrosine kinase that specifically phosphorylates a negative regulatory site of p60c-src.
    Nature. 1991 May 2;351(6321):69-72 PMID: 1709258
  2. cyl encodes a putative cytoplasmic tyrosine kinase lacking the conserved tyrosine autophosphorylation site (Y416src).
    Oncogene. 1991 Nov;6(11):2013-8 PMID: 1945408
  3. Structural differences between repressed and derepressed forms of p60c-src.
    Mol Cell Biol. 1989 Jun;9(6):2648-56 PMID: 2474758
  4. A general method for site-specific incorporation of unnatural amino acids into proteins.
    Science. 1989 Apr 14;244(4901):182-8 PMID: 2649980
  5. Specific motifs recognized by the SH2 domains of Csk, 3BP2, fps/fes, GRB-2, HCP, SHC, Syk, and Vav.
    Mol Cell Biol. 1994 Apr;14(4):2777-85 PMID: 7511210
  6. Rapid and efficient purification of Src homology 2 domain-containing proteins: Fyn, Csk and phosphatidylinositol 3-kinase p85.
    Biochem J. 1994 Sep 15;302 ( Pt 3):737-44 PMID: 7524477
  7. Evaluation of the catalytic mechanism of recombinant human Csk (C-terminal Src kinase) using nucleotide analogs and viscosity effects.
    J Biol Chem. 1994 Dec 9;269(49):30880-7 PMID: 7527038
  8. Structure-function relationships in Src family and related protein tyrosine kinases.
    Bioessays. 1995 Apr;17(4):321-30 PMID: 7537961
  9. Peptide ligation and semisynthesis.
    Curr Opin Biotechnol. 1995 Aug;6(4):403-10 PMID: 7579650
  10. A designed peptide ligase for total synthesis of ribonuclease A with unnatural catalytic residues.
    Science. 1994 Oct 14;266(5183):243-7 PMID: 7939659
  11. Synthesis of proteins by native chemical ligation.
    Science. 1994 Nov 4;266(5186):776-9 PMID: 7973629
  12. Detection of a physical and functional interaction between Csk and Lck which involves the SH2 domain of Csk and is mediated by autophosphorylation of Lck on tyrosine 394.
    J Biol Chem. 1996 Mar 29;271(13):7465-72 PMID: 8631775
  13. Regulation, substrates and functions of src.
    Biochim Biophys Acta. 1996 Jun 7;1287(2-3):121-49 PMID: 8672527
  14. Correlation of the phosphorylation states of pp60c-src with tyrosine kinase activity: the intramolecular pY530-SH2 complex retains significant activity if Y419 is phosphorylated.
    Biochemistry. 1996 Jul 23;35(29):9519-25 PMID: 8755732
  15. Chaperone-assisted protein expression.
    Structure. 1996 Mar 15;4(3):239-42 PMID: 8805540
  16. The mechanism of protein splicing and its modulation by mutation.
    EMBO J. 1996 Oct 1;15(19):5146-53 PMID: 8895558
  17. The leucine zipper domain controls the orientation of AP-1 in the NFAT.AP-1.DNA complex.
    Chem Biol. 1996 Dec;3(12):981-91 PMID: 9000009
  18. Three-dimensional structure of the tyrosine kinase c-Src.
    Nature. 1997 Feb 13;385(6617):595-602 PMID: 9024657
  19. Crystal structure of the Src family tyrosine kinase Hck.
    Nature. 1997 Feb 13;385(6617):602-9 PMID: 9024658
  20. Activation of the Src-family tyrosine kinase Hck by SH3 domain displacement.
    Nature. 1997 Feb 13;385(6617):650-3 PMID: 9024665
  21. Divalent ion effects and insights into the catalytic mechanism of protein tyrosine kinase Csk.
    Biochemistry. 1997 Feb 18;36(7):1874-81 PMID: 9048573
  22. Single-column purification of free recombinant proteins using a self-cleavable affinity tag derived from a protein splicing element.
    Gene. 1997 Jun 19;192(2):271-81 PMID: 9224900
  23. The activated form of the Lck tyrosine protein kinase in cells exposed to hydrogen peroxide is phosphorylated at both Tyr-394 and Tyr-505.
    J Biol Chem. 1997 Oct 10;272(41):25429-32 PMID: 9325251
  24. Protein synthesis by chemical ligation of unprotected peptides in aqueous solution.
    Methods Enzymol. 1997;289:266-98 PMID: 9353726
  25. Peptide and protein phosphorylation by protein tyrosine kinase Csk: insights into specificity and mechanism.
    Biochemistry. 1998 Jan 6;37(1):165-72 PMID: 9425036
  26. Expressed protein ligation, a novel method for studying protein-protein interactions in transcription.
    J Biol Chem. 1998 Jun 26;273(26):16205-9 PMID: 9632677
Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1998-06-09
Pages
6705-10
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC22605
Subset
IM
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com