1 / 4

Utilizzo della tecnologie BIacore nello studio delle interazioni proteina-proteina e proteina ligando

Marco VANONI. Utilizzo della tecnologie BIacore nello studio delle interazioni proteina-proteina e proteina ligando. DIPARTIMENTO DI BIOTECNOLOGIE E BIOSCIENZE. BIAcore (Biomolecular interaction analysis): principles. BIAcore : applications. Specificity

etta
Download Presentation

Utilizzo della tecnologie BIacore nello studio delle interazioni proteina-proteina e proteina ligando

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Marco VANONI Utilizzo della tecnologie BIacore nello studio delle interazioni proteina-proteina e proteina ligando DIPARTIMENTO DI BIOTECNOLOGIE E BIOSCIENZE

  2. BIAcore (Biomolecular interaction analysis): principles

  3. BIAcore : applications • Specificity • The extent to which different molecules interact with a single partner immobilized on a sensor surface reveals the specificity of an interaction • Qualitative (Yes/No) answers • Search for binding partners • Screen for inhibitor specificity • Test for cross-reactivity • Look for activity after purification • Kinetics and affinity determination • The kinetics of an interaction, i.e. the rates of complex formation (kon) and dissociation (koff) can be determined from the information present in a sensorgram, by fitting the data to interaction models. • For a simple 1:1 interaction, the equilibrium constant KD is the ratio of the kinetic rate coinstants, koff/kon • Concentration • Determined by monitoring the interaction of a molecule with a prepared sensor surface in the presence of a target molecule in solution (solution inhibition) or excess analyte (surface competition). Concentrations are calculated by interpolation of the binding responses on a calibration curve • Multiple interactions during complex formation • Complex formation can be monitored as each component is incorporated into a multimolecular complex

  4. Phosphorylation-dependent binding of a Cki to a cyc/Cdk complex Probing prion fibril formation 450 400 350 300 RU 250 200 150 100 50 Barberis M et al, BBRC (2005) 336:1040-8 0 -50 0 50 100 150 200 250 300 350 Time (sec) Inhibiting Ras/Gef interaction with LMW compounds Unpublished (in collaboration with F Peri) Gobbi M et al, J Biol Chem (2006) 281:843-9 BIAcore (Biomolecular interaction analysis): examples

More Related