contreras-martin research group laboratory of molecular engineering
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Engineering at the interface of RNA-protein complexes for solving difficult problems in biology and medicine . Contreras-Martin Research Group Laboratory of Molecular Engineering University of Texas at Austin Department of Chemical Engineering Austin, TX 78712 USA. - PowerPoint PPT PresentationTRANSCRIPT
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Engineering at the interface of RNA-protein complexes for solving difficult
problems in biology and medicine
Contreras-Martin Research GroupLaboratory of Molecular Engineering
University of Texas at AustinDepartment of Chemical Engineering
Austin, TX 78712 USA
Graduate Recruiting Weekend- 2.26.2011
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Contreras-Martin Research Lab Graduate Recruiting Weekend- 2.26.2011
What does Artic foxes and drug-resistant bacteria have in common?
Summer Environment Summer Environment
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A challenge in fighting pathogenic bacteria
• Disease-causing microbes that have become resistant to antibiotic drug therapy are an increasing public health problem.
• ~ 70 percent of the bacteria that cause infections in hospitals are resistant to at least one of the drugs most commonly used for treatment.
Contreras-Martin Research Lab Graduate Recruiting Weekend- 2.26.2011
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RNA-protein complexes: key anti-bacterial targets
“Possibly the most pregnant recent development in molecular biology is the realization that the beginnings of life are closely associated with the interactions of proteins and nucleic acids” — Florence O. BellExample: Bacterial ribosome critical for survival (Nobel Prize, 2009)
Contreras-Martin Research Lab Graduate Recruiting Weekend- 2.26.2011
Chloramphenicol, Erythromycin, Neomycin, Gentamicin Tetracycline, Thiostrepton, Spiramycin…
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Molecular aspects of RNA-based recognition
Challenge: Understanding how to discriminate among all cellular molecules for recognition of a specific target RNA
E. coli cytoplasm ~6mg/ml RNA• Structural and chemical features of RNAs that allow them to be recognized as drug targets?
• How do these interactions rearrange with environmental changes?
• How do they recognize their natural targets?
Contreras-Martin Research Lab Graduate Recruiting Weekend- 2.26.2011
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Graduate Recruiting Weekend- 2.26.2011
Engineering RNAs and RNA-targeting molecules with novel functionality
Can we exploit these sophisticated recognition methods for the design and development of new
biotechnologically and therapeutically relevant RNAs?
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Graduate Recruiting Weekend- 2.26.2011
Understanding and Engineering RNAs
Approach 1: Gain mechanistic
insights about RNA-protein recognition
Approach 3:Design of new RNA
molecules and RNA-targeting
compounds with novel functionality
Approach 2: Exploit features of
intermolecular interactions for
new biotechnological
tools•Modeling Techniques
Engineer molecular tools to study:• Structure • Particle physics• Chemical composition
• reconfigure cellular behavior• Controllable RNA elements• RNA-based sensors• Predict resistance
• Random mutagenesis•Rational design•De novo design
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Contact Information
Dr. Lydia Contreras-MartinOffice: 5.410 CPE
Email: [email protected]: 512-471-2453
Graduate Recruiting Weekend- 2.26.2011