Abstract
The interaction between the antitumor drug nitrullin and the system providing the transport ofl-lysine into P388 leukemic cells and murine enterocytes is studied. Two types of lysine carriers with low and high affinity for the substrate are identified. Nitrullin competitively inhibits the transport of3H-lysine and shows the same affinity for both carriers. It is similar to that of lysine for the low-affinity carrier and is 80-fold lower than lysine affinity for the high-affinity carrier. Kinetic characteristics of the low-affinity transport of3H-lysine and Ki of nitrullin are similar to those obtained at a reciprocal substrate-inhibitor ratio. Nitrullin does not inhibit active transport of3H-lysine into enterocytes against the background of considerable (70%) passive diffusion.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
