Biomolecule Crystallization Microarray

Award Information
Agency: Department of Health and Human Services
Branch: N/A
Contract: 2R42RR017138-02
Agency Tracking Number: RR017138
Amount: $1,188,691.00
Phase: Phase II
Program: STTR
Awards Year: 2004
Solicitation Year: N/A
Solicitation Topic Code: N/A
Solicitation Number: N/A
Small Business Information
SPACE HARDWARE OPTIMIZATION TECHNOLOGY
SPACE HARDWARE OPTIMIZATION, TECHNOLOGY, INC., GREENVILLE, IN, 47124
DUNS: N/A
HUBZone Owned: N
Woman Owned: N
Socially and Economically Disadvantaged: N
Principal Investigator
 PAUL TODD
 (812) 923-9591
 PTODD@SHOT.COM
Business Contact
 MARK DEUSER
Phone: (812) 923-9591
Email: MDEUSER@SHOT.COM
Research Institution
 UNIVERSITY OF MINNESOTA
 UNIVERSITY OF MINNESOTA
Minneapolis, MN, 55455
 Nonprofit college or university
Abstract
DESCRIPTION (provided by applicant): Several aspects of health and medicinal research depend on the knowledge of macromolecular structures, the determination of which depends on a supply of high-quality crystals. Conditions for growing high-quality crystals are usually determined by expensive trial-and-error research. The proposed innovation is a lithography-fabricated system for automated, kinetically controlled growth of biomolecule crystals for crystallography. It is also useful in crystallization process development applications. An array of crystallization chambers, each with a volume of a few microlitres is served by an array of pumps whose feed rates are controlled in the sub-nL/s range by a time-of-flight flow meter. The pumps, one each for buffer, biomolecule solution and precipitant solution, are commanded by control algorithms that use image data. The individual concepts were demonstrated in Phase I research, namely, the ability to deliver a few microlitres of solution to a microreactor chamber over several hours and to grow crystals in such a chamber, the ability to electronically measure sub nL/s flow rates with a meter than has no moving parts, and the identification of a very inexpensive digital imaging and analysis method. The Phase II research specific aims are to (1) integrate these novel components into a single automated crystallization system to be tested for the coordination of all functions through a single control computer; (2) on the basis of (1) design and fabricate by lithography an integrated 4-chamber array including optics, microfluidics and electronics; and (3) test this array against real crystal-growth problems and refine image-based control algorithms. This technology uses automated kinetic control of the liquid-liquid crystallization method as a means of canvassing a continuum of chemical conditions rather than using massively paralleled discreet screening to enhance throughput in this rather expensive process. The resulting product, a crystallizer microarray ("CRYMA"), will be marketed to the world's large pharmaceutical firms, university laboratories with structural biology units and governmental space research agencies - a market with which SHOT, Inc. is familiar. Its implementation.

* information listed above is at the time of submission.

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