Opto-Fluidic Array for Radical Protein Foot-Printing
AssigneeGennext Technologies, Inc.
InventorsScot Randy Weinberger, Robert Wallace Egan, Jeffrey Johnathan Persoff, Emily Elizabeth Chea, Tan Huu Bui, David Allan Holman
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Abstract
Systems and methods of in vivo and in vitro radical protein foot-printing using an opto-fluidic array are presented. These teachings may be used to, for example, study three-dimensional protein structure or bio-kinetics. Radical dosimetry including an optional intrinsic standard is used. Real-time feedback based on an internal standard provides comparability between different experiments and in vivo and in vitro analysis results in data that is representative of actual biological conditions.
Claims11
A method for use in conjunction with an opto-fluidic array comprising a photolysis zone, a photolysis light source, a dosimetry zone, and a dosimetry light source, the method comprising:
- introducing into the photolysis zone a mixture including a biological entity, a chemical compound, and a dosimeter internal standard;
- providing a light pulse from the photolysis light source to the photolysis zone, wherein the light pulse is one pulse in a series of periodic light pulses, to generate a concentration of radicals from the chemical compound, the radicals being effective to react with the dosimeter internal standard;
- providing light to the dosimetry zone from the dosimetry light source and, after the light from the photolysis light source is provided to the photolysis zone, detecting a change in light received from within the dosimetry zone, the change in the received light being indicative of the biological entity being within the dosimetry zone, and measuring a photometric property of the dosimeter internal standard within the dosimetry zone;
- determining that the measured photometric property is below a threshold;
- and
- determining a change to be applied to the opto-fluidic array to bring the measured photometric property to the threshold, the change comprising a change to an amount of light provided by the photolysis light source, a change of a concentration of the chemical compound in the mixture, a change to a flow rate of the mixture through the photolysis zone, or adjusting a phase of the periodic pulses.
A method for sheath flow control in an opto-fluidic array comprising a dosimetry zone, a dosimetry light source, and a sheath flow generator, the method comprising:
- introducing into the sheath flow generator a mixture including a plurality of cells, a chemical compound, and a dosimeter internal standard, and further introducing into the sheath flow generator a buffer wherein the sheath flow generator is effective to employ hydrodynamic focusing to pass therefrom the mixture including the plurality of cells, wherein the cells of the plurality of cells are passed individually with uniform spacings therebetween;
- receiving the mixture from the sheath flow generator into the dosimetry zone and providing a light from the dosimetry light source to the dosimetry zone while monitoring light received from the dosimetry zone, the received light varying with a periodicity as the cells individually pass through the dosimetry zone;
- and
- adjusting a flow rate of the mixture, or a flow rate of the buffer, into the sheath flow generator to control the periodicity.
Dependencies are inferred from the claim text.