8
Cell-Free
Protein Synthesis for High-Through-Put Proteomics--MacConnell
Research Corporation, 6195 Cornerstone Court East, #114, San Diego, CA
92121-4728; 858-452-2603, www.macconnell.com
Dr.
William P. MacConnell, Principal Investigator, bmacconnell@macconnell.com
Dr.
William P. MacConnell, Business Official, bmacconnell@macconnell.com
DOE
Grant No. DE-FG02-03ER83706
Amount:
$735,298
The
production of proteins from cloned DNA sequences is an important process for
functional genomic studies and structural analysis, as well as many other
research applications, including pharmaceutical drug discovery.
This project will develop in vitro
protein synthesis reagents and instrumentation that will produce highly active,
robust protein using a universally applicable protocol.
The system will generate 100 milligrams or more of active protein, allow
it to synthesize multiple proteins in one reaction, and allow the process to
begin with PCR (polymerase chain reaction) amplified DNA.
The system will provide a tremendous advantage in simplicity and cost
over in vivo protein expression
methods in that it simplifies or eliminates vector construction, cell
transfection, protein induction, and uncertainties of host cell synthesis. Phase
I demonstrated that enhanced S30 wheat germ lysate could be made, that it could
generate up to 30 milligrams of protein in one reaction, that the protein it
generated was enzymatically active, and that the process could begin with either
plasmid or PCR-generated template DNA. Seven
different proteins of varying sizes were synthesized from bacterial and
mammalian origin. The synthesized
protein was successfully purified from the reaction mixture using a simple,
one-step affinity purification method. Phase
II will improve the system to allow for: (1)
the generation of 100 milligrams or more of active protein, synthesis of
multiple proteins in one reaction; (2) the process to begin with PCR amplified
DNA; (3) affinity purification; and (4) the sale of these products at affordable
prices, thus making the methodology available to any laboratory.
Commercial
Applications and Other Benefits as
described by awardee: The technology
should generate several products that can be sold directly to the 50,000 or more
laboratories throughout the world that perform genomic and proteomic research.
We project that purified protein can be synthesized by these products for
less then $11 per milligram. In
addition, a simplified instrument can be developed and marketed that will
automate the incubation and substrate addition steps of the procedure.
The instrument, which should cost less then $2,000, can be marketed with
the reagent kits. These products
will save countless man hours of time, improve the outcome of experiments, and
represent a tremendous cost saving to laboratories.