The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.
The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.
Patent No.:
Date of Patent:
May. 14, 2013
Filed:
Feb. 23, 2011
Ronald R. Breaker, Guilford, CT (US);
Ali Nahvi, New Haven, CT (US);
Narasimhan Sudarsan, New Haven, CT (US);
Margaret S. Ebert, Hopewell, NJ (US);
Wade Winkler, Dallas, TX (US);
Jeffrey E. Barrick, Lansing, MI (US);
John K. Wickiser, Cornwall on Hudson, NY (US);
Ronald R. Breaker, Guilford, CT (US);
Ali Nahvi, New Haven, CT (US);
Narasimhan Sudarsan, New Haven, CT (US);
Margaret S. Ebert, Hopewell, NJ (US);
Wade Winkler, Dallas, TX (US);
Jeffrey E. Barrick, Lansing, MI (US);
John K. Wickiser, Cornwall on Hudson, NY (US);
Yale University, New Haven, CT (US);
Abstract
It has been discovered that certain natural mRNAs serve as metabolite-sensitive genetic switches wherein the RNA directly binds a small organic molecule. This binding process changes the conformation of the mRNA, which causes a change in gene expression by a variety of different mechanisms. Modified versions of these natural 'riboswitches' (created by using various nucleic acid engineering strategies) can be employed as designer genetic switches that are controlled by specific effector compounds. Such effector compounds that activate a riboswitch are referred to herein as trigger molecules. The natural switches are targets for antibiotics and other small molecule therapies. In addition, the architecture of riboswitches allows actual pieces of the natural switches to be used to construct new non-immunogenic genetic control elements, for example the aptamer (molecular recognition) domain can be swapped with other non-natural aptamers (or otherwise modified) such that the new recognition domain causes genetic modulation with user-defined effector compounds. The changed switches become part of a therapy regimen—turning on, or off, or regulating protein synthesis. Newly constructed genetic regulation networks can be applied in such areas as living biosensors, metabolic engineering of organisms, and in advanced forms of gene therapy treatments.