Minimal FLAG Sequence Useful in the Functional Epitope Tagging of H-Ras
Author(s) -
Kristy Y. Johnson,
Liya Liu,
Timothy S. Vincent
Publication year - 2002
Publication title -
biotechniques
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.617
H-Index - 131
eISSN - 1940-9818
pISSN - 0736-6205
DOI - 10.2144/02326st02
Subject(s) - flag (linear algebra) , epitope , sequence (biology) , biology , peptide sequence , computational biology , microbiology and biotechnology , genetics , sequence analysis , gene , antibody , mathematics , pure mathematics , algebra over a field
Epitope tagging can interfere with normal protein function, indicating the need for an unobtrusive epitope tag. The FLAG ® epitope (DYKDDDDK) was examined for a minimal epitope useful in the tagging of HRas. The heptapeptide tag, F7 (MDYKD-DD), was found to retain reactivity with M2 and M5 monoclonal antibodies in immunoprecipitation, Western blotting, and immunofluorescence microscopy. The F7 tag did not interfere with Ras stability, EGF stimulation of Ras activation, and downstream phosphorylation of MAPK Erk1/2. Unlike the full FLAG sequence, the F7 tag had minimal effect on the growth properties of H-Ras in a colony-forming assay. The F7 tag may be useful when minimizing the effect of tagging on protein function is an important criterion in the selection of an N-terminal epitope tag.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom