SBIR/STTR Research Award
High through-put chemical synthesis of proteins
Award amount
$167,164Program and phase
SBIR · Phase IAward year
2001Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- PROSYNTH, INC.
- Proposal award date
- Not reported
- Contract end date
- Not reported
- UEI
- Not reported
- Solicitation number
- Not reported
- Topic code
- Not reported
Research abstract
DESCRIPTION (provided by applicant):The objectives of the Protein Structure
Initiative is to determine the structure of 10,000 proteins from the Human
Genome Project. Chemical synthesis is a useful way to produce these proteins
particularly when they cannot be efficiently cloned.
ProSynth, Inc. has developed technology that allows the synthesis of pure,
protected fragments at relatively low cost. In the Excluded Protecting Group
method a growing peptide is attached to a steroid "handle" and purified by gel
permeation chromatography after addition of each amino acid residue.
Orthogonally protected peptides synthesized this way can then be coupled either
in solution or on the solid phase.
ProSynth, Inc. will demonstrate its technology by the synthesis and coupling of
two peptide fragments that make up the 26-residue protein melittin. This
peptide will be characterized for purity and tested for biological activity.
In a second experiment the EPG technique will be used to prepare the protein
ubiquitin. The six fragments ranging from six to 22 amino acids will be
synthesized and to generate the desired product. The focus of this synthesis
will be to determine the reaction order for various couplings in order to
predict when a desired degree of coupling has been reached.
PROPOSED COMMERCIAL APPLICATION:
This technology will allow proteins to be designed and produced. This should allow
for protein drugs to be improved yielding superior protein drugs for clinical application.
Technology keywords
Not reported