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Inhibition of Bcr-Abl kinase activity by d-monobodies After showing binding to the Bcr-Abl SH2 domain with high affinity, we next wanted to assess a possible inhibitory effect of monobodies on Bcr-Abl kinase activity in vitro

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However, it is necessary to consider that the introduction of a new amide bond increases the susceptibility to hydrolysis and the topological polar surface area (TPSA), as well as contributing to the increase of hydrogen bond donor (HBD) or hydrogen bond acceptor (HBA) count

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This molecular alteration ensures tumor cell survival and proliferation in the microenvironment with low physiological serine concentrations

Circulation 1983