Lectin-mediated microfluidic capture and release of leukemic lymphocytes from whole blood |
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Authors: | Dwayne A. L. Vickers Marina Hincapie William S. Hancock Shashi K. Murthy |
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Affiliation: | (1) Department of Chemical Engineering, Northeastern University, 360 Huntington Ave. 342 SN, Boston, MA 02115, USA;(2) Barnett Institute and Department of Chemistry & Chemical Biology, Northeastern University, Boston, MA, USA; |
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Abstract: | Lectins are a group of proteins that bind specifically and reversibly to mono- and oligosaccharide carbohydrate structures that are present on the surfaces of mammalian cells. The use of lectins as capture agents in microfluidic channels was examined with a focus on cells associated with T and B lymphocytic leukemia. In addition to examining the adhesion of Jurkat T and Raji B lymphocytes to a broad panel of lectins, this work also examined the capture of these cells from whole blood. Captured T and B lymphocytes were eluted from the microfluidic devices with a solution of the lectin’s inhibiting sugar. The capture and release steps were accomplished in under 1 h. The significance of this work lies within the realm of low-cost capture of abundant target cells with non-stimulatory elution capability. |
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