Design, synthesis and binding properties of a fluorescent alpha sub(9) beta sub(1)/ alpha sub(4) beta sub(1) integrin antagonist and its application as an in vivoprobe for bone marrow haemopoietic stem cells
The alpha sub(9) beta sub(1) and alpha sub(4) beta sub(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 sub(4) beta sub(1) integrin have been thoroughly investigated with respect to...
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Published in | Organic & biomolecular chemistry Vol. 12; no. 6; pp. 965 - 978 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
01.01.2014
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Online Access | Get full text |
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Summary: | The alpha sub(9) beta sub(1) and alpha sub(4) beta sub(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 sub(4) beta sub(1) integrin have been thoroughly investigated with respect to HSC function, the role of alpha sub(9) beta sub(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 sub(9) beta sub(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 sub(9) beta sub(1) integrin with potent cross-reactivity against alpha sub(4) beta sub(1) integrin under physiological mimicking conditions. On-rate and off-rate measurements revealed distinct differences in the binding kinetics between alpha sub(9) beta sub(1) and alpha sub(4) beta sub(1) integrins, which showed faster binding to alpha sub(4) beta sub(1) integrin relative to alpha sub(9) beta sub(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 sub(9) beta sub(1) and alpha sub(4) beta sub(1) integrins; (2) investigating the biochemical properties of alpha sub(9) beta sub(1) and alpha sub(4) beta sub(1) integrin binding and (3) investigating integrin expression and activation on defined cell phenotypes in vivo. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 content type line 23 ObjectType-Feature-1 |
ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/c3ob42332h |