A new approach for the characterization of the C-terniiiials of proteins has been developed. The strategy involves three steps. First, the protein is degraded enzymatically with trypsin or Lys-C. Second the C-tenninal peptide is separated from all the other proteolysis products through the use of anhydrotrypsin, a modified trypsin that binds only peptides containing K or R at the C-terminus. Finally, the C-terminal peptide is characterized by MALDI. The strategy was tested and shown to work well on a series of designed synthetic peptides as well as on the transcription factor Hairy, where the C-terminal peptide was readily isolated and identified.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR000862-27
Application #
6307531
Study Section
Project Start
1999-12-01
Project End
2000-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
27
Fiscal Year
2000
Total Cost
$8,199
Indirect Cost
Name
Rockefeller University
Department
Type
DUNS #
071037113
City
New York
State
NY
Country
United States
Zip Code
10065
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