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A more recent version of this article appeared on December 1, 2007.
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Submitted on January 24, 2007
Revised on September 12, 2007
Accepted on September 17, 2007

Aptamer directly evolved from live cells recognizes membrane bound immunoglobin heavy mu chain in Burkitt's lymphoma cells

Prabodhika Mallikaratchy, Zhiwen Tang, Ling Meng, Dihua Shangguan, Sefah Kwame, and Weihong Tan

Department of Chemistry, University of Florida, Gainesville, FL 32611-7200

Corresponding Author: tan{at}chem.ufl.edu

The identification of tumor related cell membrane protein targets is important in understanding tumor progression, the development of new diagnostic tools, and potentially for identifying new therapeutic targets. Here we present a novel strategy for identifying uniquely expressed proteins using cell specific aptamers. Using an intact viable B-cell Burkitt’s lymphoma cell line (Ramos cells) as the target, we have selected aptamers that recognize cell membrane proteins with high affinity. Among the selected aptamers that showed unique recognition patterns with different cell lines of leukemia, the aptamer TD05 showed binding only with Ramos cells. By chemically modifying TD05 to covalently crosslink with its target on Ramos cells and to capture and enrich the target receptors using streptavidin coated magnetic beads followed by mass spectrometry, we were able to identify membrane bound Immunoglobin Heavy mu chain (IGHM) as the target for TD05 aptamer. IGHM is a major component of B-Cell antigen receptor (BCR) which is uniquely expressed in B-Cells. This study demonstrates that this two-step strategy, the development of high-quality aptamer probes and then the identification of their target proteins, can be used to discover new disease-related potential markers and thus enhance tumor diagnosis and therapy. The aptamer based strategy will enable effective molecular elucidation of disease related biomarkers and other interesting molecules.







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