20.109(S11):Module 1

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Current revision (14:48, 31 January 2011) (view source)
 
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[[20.109(S11):Purify RNA and run affinity column (Day4)| Module 1 Day 4: Purify RNA and run affinity column]]<br>
[[20.109(S11):Purify RNA and run affinity column (Day4)| Module 1 Day 4: Purify RNA and run affinity column]]<br>
[[20.109(S11):RNA to DNA by RT-PCR (Day5)| Module 1 Day 5: RNA to DNA by RT-PCR]]<br>
[[20.109(S11):RNA to DNA by RT-PCR (Day5)| Module 1 Day 5: RNA to DNA by RT-PCR]]<br>
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Note: 1 week between day 5 and day 6.
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[[20.109(S11):Post-selection IVT and journal club (Day6)| Module 1 Day 6: Post-selection IVT and journal club]]<br>
[[20.109(S11):Post-selection IVT and journal club (Day6)| Module 1 Day 6: Post-selection IVT and journal club]]<br>
[[20.109(S11):Aptamer binding assay (Day7)| Module 1 Day 7: Aptamer binding assay]]<br>
[[20.109(S11):Aptamer binding assay (Day7)| Module 1 Day 7: Aptamer binding assay]]<br>

Current revision

20.109(S11): Laboratory Fundamentals of Biological Engineering

Home        People        Schedule Spring 2011        Assignments        Lab Basics        OWW Basics       
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Module 1

Instructors: Jacquin Niles and Agi Stachowiak

TA: Carrie Thompson

In this module you will investigate RNA aptamer selection. You may already be familiar with biological entities that bind to specific molecules, such as antibody proteins or their peptide derivatives. Short fragments of RNA can also have high-order structures that allow them to bind a target molecule with good affinity and specificity; successful binders are called aptamers. Normally, RNA aptamers that bind particular targets are found by screening many candidates at random in a process called SELEX, or systematic evolution of ligands by exponential enrichment. (Predictive computational tools can also be used to design rather than select aptamers.) In the coming weeks, you will essentially perform one round of SELEX. Because SELEX typically takes several rounds to isolate target-binding aptamers, you will start with a known RNA mixture rather than than a completely random library. Your goal will be to explore what experimental parameters affect the enrichment of a heme-binding RNA aptamer from a mixture of heme-binding and non-binding RNAs.

We thank 20.109 instructor Natalie Kuldell for helpful discussions and for acquiring funding for module development.

Structure of a putative aptamer Image was prepared using RNA folding at http://mfold.bioinfo.rpi.edu/
Structure of a putative aptamer Image was prepared using RNA folding at http://mfold.bioinfo.rpi.edu/


Module 1 Day 1: Amplify aptamer-encoding DNA
Module 1 Day 2: Purify aptamer-encoding DNA
Module 1 Day 3: Prepare RNA by IVT
Module 1 Day 4: Purify RNA and run affinity column
Module 1 Day 5: RNA to DNA by RT-PCR

Note: 1 week between day 5 and day 6.

Module 1 Day 6: Post-selection IVT and journal club
Module 1 Day 7: Aptamer binding assay
Module 1 Day 8: Journal club

Laboratory Report
Computational analysis

TA notes, mod 1
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