Integrated Cancer Research Center Seminar Series

*********************************
There is now a CONTENT FREEZE for Mercury while we switch to a new platform. It began on Friday, March 10 at 6pm and will end on Wednesday, March 15 at noon. No new content can be created during this time, but all material in the system as of the beginning of the freeze will be migrated to the new platform, including users and groups. Functionally the new site is identical to the old one. webteam@gatech.edu
*********************************

Event Details
  • Date/Time:
    • Tuesday February 27, 2018 - Wednesday February 28, 2018
      4:00 pm - 4:59 pm
  • Location: Petit Biotechnology Building, Room 1128 - Atlanta, GA
  • Phone:
  • URL:
  • Email:
  • Fee(s):
    N/A
  • Extras:
Contact

John McDonald - faculty host

Summaries

Summary Sentence: "CompELS: A Nonevolutionary Screening Approach for DNA Aptamers" - Valeria Milam, Ph.D. - Georgia Tech

Full Summary: No summary paragraph submitted.

"CompELS: A Nonevolutionary Screening Approach for DNA Aptamers"

Valeria Milam, Ph.D.
Associate Professor
Georgia Tech

Oligonucleotide aptamers are single-stranded sequences that exhibit high affinity and specificity for a particular nonnucleotide target. To date, aptamer studies typically entail an evolutionary-based screening approach called "Systematic Evolution of Ligands by EXponential Enrichment" (SELEX). SELEX has revolutionized the discovery of numerous DNA and RNA-based aptamers and dominated the field for over two decades as a screening approach; however, SELEX itself is a labor-intensive process with pitfalls such as its propensity to introduce PCR-based sequence bias and contaminants. Here, we have developed a nonevolutionary screening approach we call CompELS (Competition Enhanced Ligand Selection) to rapidly and reliably identify single-stranded DNA aptamers for a model target, namely gold. Following aptamer selection against our target we then evaluated winning sequences to identify base segment consensus as well as any shared and unshared patterns in their predicted secondary structure elements such as hairpins, internal loops, and multi-branched loops. Lastly, in a separate post-screening competition experiment, we ranked our aptamer candidates in terms of their frequency as a bound species using next generation sequencing and identified multiple high affinity aptamers. As aptamers continue to be pursued as potential ligands or capture agents in the biology and bioengineering community, our ongoing and future efforts include adapting our unconventional screening approach to enable faster and easier aptamer identification for challenging biological targets.

Related Links

Additional Information

In Campus Calendar
Yes
Groups

Parker H. Petit Institute for Bioengineering and Bioscience (IBB)

Invited Audience
Faculty/Staff, Graduate students
Categories
Seminar/Lecture/Colloquium
Keywords
go-PetitInstitute, go-icrc, go-icrc-events, ICRC, ICRC Seminar
Status
  • Created By: Floyd Wood
  • Workflow Status: Published
  • Created On: Jan 11, 2018 - 10:54am
  • Last Updated: Feb 23, 2018 - 10:56am