Understanding SELEX to Systematic Evolution of Ligands

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SUMMARY

SELEX, or systematic evolution of ligands by exponential enrichment, is a robust technique for identifying high-affinity DNA or RNA sequences that bind to specific protein targets. The process begins with a diverse pool of random sequences mixed with a nucleic acid binding protein (NBP), followed by amplification of the sequences that exhibit strong binding. This iterative selection process enhances the concentration of the most effective sequences, ultimately yielding those with the highest affinity for the NBP. Key references include the original paper by Turek and Gold (1990) and a classic application of SELEX for histone proteins.

PREREQUISITES
  • Understanding of nucleic acid binding proteins (NBPs)
  • Familiarity with DNA and RNA sequence amplification techniques
  • Knowledge of evolutionary principles applied to molecular biology
  • Basic comprehension of experimental design in biochemistry
NEXT STEPS
  • Study the original SELEX methodology as described in Turek and Gold, 1990
  • Explore advanced applications of SELEX in therapeutic development
  • Investigate the use of SELEX for identifying RNA aptamers
  • Learn about the graphical representation of SELEX results in scientific literature
USEFUL FOR

Researchers in molecular biology, biochemists, and professionals involved in drug discovery and development who are interested in high-affinity ligand identification techniques.

hivesaeed4
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Could someone explain SELEX (systematic evolution of ligands by exponential enrichment) or at least direct me to a good resource online because so far I have'nt found a decent explanation or website regarding SELEX online.
 
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Don't bother. I've found something which will help me.
 
SELEX is a technique to identify DNA or RNA sequences that bind to a protein target with high affinity. The method uses principles from evolution to accomplish this goal. You start out with a large pool of random DNA or RNA sequences. You then mix these sequences with your nucleic acid binding protein (NBP) in order to isolate the sequences that bind to the NBP the best. Next, you amplify the sequences isolated from the binding step then repeat the procedure by binding these sequences to your NBP again.

As you perform more and more cycles of selection, the DNA or RNA sequences that bind to the NBP get amplified while the sequences that do not bind the NBP do not get amplified. Soon, the pool of sequences consists of only the most "fit" sequences that bind to the NBP with the highest affinity.

Here's the citation for the original paper describing the SELEX method:
Turek and Gold, 1990. Systematic Evolution of Ligands by Exponential Enrichment: RNA Ligands to Bacteriophage T4 DNA Polymerase. Science, 249: 505. http://dx.doi.org/10.1126/science.2200121[/url .

Here's a link to a classic paper applying the SELEX method to find sequences that bind strongly to histone proteins. Figure 1 shows a nice graphical overview of the method:
http://groups.molbiosci.northwestern.edu/widomweb/pdfpapers/New%20DNA%20Sequence%20Rules%20for%20High.pdf
 
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