Journal
ORGANIC & BIOMOLECULAR CHEMISTRY
Volume 12, Issue 6, Pages 965-978Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3ob42332h
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The alpha(9)beta(1) and alpha(4)beta(1) integrin subtypes are expressed on bone marrow haemopoietic stem cells and have important roles in stem cell regulation and trafficking. Although the roles of alpha(4)beta(1) integrin have been thoroughly investigated with respect to HSC function, the role of alpha(9)beta(1) integrin remains poorly characterised. Small molecule fluorescent probes are useful tools for monitoring biological processes in vivo, to determine cell-associated protein localisation and activation, and to elucidate the mechanism of small molecule mediated protein interactions. Herein, we report the design, synthesis and integrin-dependent cell binding properties of a new fluorescent alpha(9)beta(1) integrin antagonist (R-BC154), which was based on a series of N-phenylsulfonyl proline dipeptides and assembled using the Cu(I)-catalyzed azide alkyne cycloaddition (CuAAC) reaction. Using transfected human glioblastoma LN18 cells, we show that R-BC154 exhibits high nanomolar binding affinities to alpha(9)beta(1) integrin with potent cross-reactivity against alpha(4)beta(1) integrin under physiological mimicking conditions. On-rate and off-rate measurements revealed distinct differences in the binding kinetics between alpha(9)beta(1) and alpha(4)beta(1) integrins, which showed faster binding to alpha(4)beta(1) integrin relative to alpha(9)beta(1), but more prolonged binding to the latter. Finally, we show that R-BC154 was capable of binding rare populations of bone marrow haemopoietic stem and progenitor cells when administered to mice. Thus, R-BC154 represents a useful multi-purpose fluorescent integrin probe that can be used for (1) screening small molecule inhibitors of alpha(9)beta(1) and alpha(4)beta(1) integrins; (2) investigating the biochemical properties of alpha(9)beta(1) and alpha(4)beta(1) integrin binding and (3) investigating integrin expression and activation on defined cell phenotypes in vivo.
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