Fig. 4.
Fig. 4. Human and mouse Lu-Fc bind laminin 10/11 specifically and with high affinity. / Binding of human laminin 10/11 to recombinant Lu-Fc proteins was examined in an optical biosensor. (A) Human Lu-Fc bound 42-nM purified human laminin 10/11 (10/11) but not 42-nM crude human, placental laminin 2/4 (2/4), or 42-nM mouse, EHS, laminin 1(1). (B) Mouse Lu-Fc bound 42-nM purified human laminin 10/11 (10/11) but not 42-nM crude human, placental laminin 2/4 (2/4), or 42-nM mouse laminin 1(1). (C) Lu-Fc was captured on the anti-Fc surface at time −15 minutes and allowed to associate until the biosensor recorded a response of 100 arc seconds. The Lu-Fc was removed and fresh buffer (PBSt) was added at time −2.5 minutes. Soluble, human laminin 10/11 was applied (final concentration 24 nM) at time 0 minute and association was recorded for 4 minutes before the laminin was exchanged for PBSt and dissociation rate (koff) of the complex was measured. In all experiments Fc fusion proteins were applied to the anti-Fc matrix to give an instrument response of 100 arc seconds before washing with PBSt, addition of laminin at time 0 minute and measurement of laminin binding. (D) Association rates (kon) for the interaction of human Lu-Fc with human laminin 10/11 were measured at laminin concentrations in the range 0.1 to 100 nM by curve fitting using the biosensor software; representative data are shown. (E) The measured values for kon were plotted against laminin concentration and the association rate constant (kass) was derived from the gradient of this plot using the biosensor software. (F) Human Lu-Fc but not the structural analogue MUC 18-Fc (MUC18) bound 10 nM laminin 10/11.

Human and mouse Lu-Fc bind laminin 10/11 specifically and with high affinity.

Binding of human laminin 10/11 to recombinant Lu-Fc proteins was examined in an optical biosensor. (A) Human Lu-Fc bound 42-nM purified human laminin 10/11 (10/11) but not 42-nM crude human, placental laminin 2/4 (2/4), or 42-nM mouse, EHS, laminin 1(1). (B) Mouse Lu-Fc bound 42-nM purified human laminin 10/11 (10/11) but not 42-nM crude human, placental laminin 2/4 (2/4), or 42-nM mouse laminin 1(1). (C) Lu-Fc was captured on the anti-Fc surface at time −15 minutes and allowed to associate until the biosensor recorded a response of 100 arc seconds. The Lu-Fc was removed and fresh buffer (PBSt) was added at time −2.5 minutes. Soluble, human laminin 10/11 was applied (final concentration 24 nM) at time 0 minute and association was recorded for 4 minutes before the laminin was exchanged for PBSt and dissociation rate (koff) of the complex was measured. In all experiments Fc fusion proteins were applied to the anti-Fc matrix to give an instrument response of 100 arc seconds before washing with PBSt, addition of laminin at time 0 minute and measurement of laminin binding. (D) Association rates (kon) for the interaction of human Lu-Fc with human laminin 10/11 were measured at laminin concentrations in the range 0.1 to 100 nM by curve fitting using the biosensor software; representative data are shown. (E) The measured values for kon were plotted against laminin concentration and the association rate constant (kass) was derived from the gradient of this plot using the biosensor software. (F) Human Lu-Fc but not the structural analogue MUC 18-Fc (MUC18) bound 10 nM laminin 10/11.

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