The goal of the proposed project is to use structure based modeling and molecular biology techniques to increase trypsin and serine collagenase specificity for substrates with His residues at the P1 position. A variant of trypsin capable of utilizing a substrate assisted catalytic mechanism (Tn H57A) will be refined to increase its hydrolysis activity against substrates containing a His residue in the P1 position. Additionally, a His57=C6Ala variant of serine collagenase from the fiddler crab Uca pugilator will be expressed and tested against similar substrates. The serine collagenase variant is expected to have greater observable activity than the redesigned trypsin due to its unique substrate recognition attributes. The technology developed can be used to selectively cleave histidine tags from recombinant proteins.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR001081-23
Application #
6347834
Study Section
Project Start
2000-07-01
Project End
2001-06-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
23
Fiscal Year
2000
Total Cost
$136
Indirect Cost
Name
University of California San Francisco
Department
Type
DUNS #
073133571
City
San Francisco
State
CA
Country
United States
Zip Code
94143
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