| Literature DB >> 27519622 |
Hasan E Zumrut1, Mst N Ara2, George E Maio2, Nabeela A Van2, Sana Batool2, Prabodhika R Mallikaratchy3.
Abstract
We recently introduced a screening technology termed ligand-guided selection, (LIGS), to selectively identify target-specific aptamers from an evolved cell-SELEX library. Cell-SELEX utilizes a large combinatorial single-stranded oligonucleotide library and progressively selects DNA ligands against whole cells with variable DNA-binding affinities and specificities by repeated rounds of partition and amplification. LIGS exploits the partition step and introduces a secondary, pre-existing high-affinity monoclonal antibody (mAb) ligand to outcompete and elute specific aptamers towards the binding target of the antibody, not the cell. Here, using anti-CD3ε mAb against the cluster of differentiation 3 (CD3ε), as the guiding ligand against one of the domains of the T-cell Receptor (TCR) complex expressed on Jurkat.E6 cells, we discovered three specific aptamers against TCR complex expressed on an immortalized line of human T lymphocyte cells. In sum, we demonstrate that specific aptamers can be identified utilizing an antibody against a single domain of a multidomain protein complex in their endogenous state with neither post- nor pre-SELEX protein manipulation.Entities:
Keywords: Aptamer; CD3ε; Evolution; Ligand; Monoclonal antibody; T-cell Receptor
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Year: 2016 PMID: 27519622 PMCID: PMC5593316 DOI: 10.1016/j.ab.2016.08.007
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365