Dianthus - Plate-based and Microfluidics-free Affinity Screening Platform

Dianthus - Plate-based and Microfluidics-free Affinity Screening Platform

Catalog Number:
PCAS516270NAN
Mfr. No.:
Dianthus
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      • Overview
        • Dianthus is a plate-based and microfluidics-free affinity screening platform. Measurements are in solution and mass-independent - ideal for succeeding at demanding screening campaigns.

          It's not surprising that the most important drug candidates and targets are super challenging when it comes to affinity screening. Immobilization-dependent SPR struggles with affinity screening campaigns for applications involving PROTAC binary and ternary complexes, fragment libraries, and intrinsically disordered proteins. These are precisely the applications where Dianthus excels.

          Now with Spectral Shift and TRIC, two methods for measuring molecular interactions, Dianthus delivers high-quality data, has the sensitivity to detect more true binders, and requires less assay development to give you results from real-life samples.

          · Measure the broadest range of affinities
          Dianthus detects a wide range of binding affinities - picomolar to millimolar - so you catch very strong and weak binders.
          · Characterize in solution, no immobilization required
          Analyzing interactions in close-to-native conditions is ideal, especially when dealing with challenging targets. Never worry about negatively impacting your target's binding site or lacking control over equilibrium conditions, since measurements are done in solution.
          · Consume small amounts of target and compounds
          Every little bit counts. Saving on costly samples and library compounds means you can do more screening campaigns or projects.
          · Automate your affinity screening campaigns
          Get hours of uninterrupted and unattended operation with a format that's compatible with many automation solutions.

          · Hit Identification
          Finding true hits faster is the most important step in making your drug discovery workflow efficient. With Dianthus, you'll find hits quickly and move on to hit validation confidently, whether it's fragment-based or small molecule single-dose screening.
          · Lead Validation
          Spend less time sorting through the strong and weak binders. Dianthus generates easy-to-interpret affinity ranking tables and histograms to help you quickly decide on the right candidates and start lead optimization sooner.
          · Lead Optimization
          Once validation is complete, it's time to improve target specificity, selectivity, and potency. Use Dianthus to verify that binding affinities remain strong. This, combined with your ADME, toxicity, and PK/PD results, ensures you're developing the best drug candidates.

          Measuring challenging interactions between various types of molecules at times requires a different approach. So having two different modalities in the same instrument helps you cover all the types of interactions you encounter. Dianthus comes with two biophysical modalities - Spectral Shift and Temperature Related Intensity Change (TRIC) - that help you measure the strength of your challenging molecular interactions.

          Dianthus is a plate-based, microfluidics-free screening platform that easily integrates into any automated setup via gRPC framework. And with no regular maintenance, your projects don't get delayed due to downtime. Dianthus is ready whenever you need it - non-stop, 24/7.

          Please contact us at for specific academic pricing.

      • Properties
        • Other Properties
          Biophysical modalities: Spectral Shift and TRIC
          Format: 384-well plate (barcoded and sealable)
          Affinity range: pM to mM
          Data points per run: Up to 384
          Run time for 384 data points: 33 minutes (Spectral Shift); 79 minutes (Spectral Shift + TRIC)
          Time it takes to get a Kd 12-point dilution series: 60 seconds (Spectral Shift); 132 sec (Spectral Shift + TRIC)
          Sample volume/well: 20 µL
          Molecular weight range: 10^1-10^7 Da
          Temperature control: 20-25°C +/- 0.5°C (actively controlled)
          Dimensions: 61 cm W x 42 cm H x 57 cm D
          Weight: 70 kg
          Automation: Able to integrate with liquid handlers and robotics
          Compounds tested in 24 h (single dose, in duplicate, plate feeder): 7400
          Kds measured in 24 h (12-point dilution series, plate feeder): 1350
      • Applications
        • Application
          Affinity Screening
          Application Description
          · PROTACs and other small molecule protein degraders
          Development of protein degraders is a multi-step and complex process. Selecting the appropriate biochemical and biophysical methods for each step is crucial to move the drug candidates down the pipeline and to market faster and with confidence.

          Dianthus resolves the challenges presented by the characterization of binary and ternary complexes and the determination of cooperativity.

          · Fragment libraries
          Challenge
          Because your method requires a significant change in mass to measure interactions, it's difficult to identify hits from a library of fragments due to their very low molecular weight.

          Solution
          With Dianthus, you identify hits from fragment libraries with confidence because measurements are mass-independent.

          And, because Dianthus detects a broad range of affinity strengths, it's useful for hit identification when fragments bind to proteins with mM affinity and lead optimization when fragments grow to form larger compounds that bind at low nM affinities.

          · Intrinsically disordered proteins (IDPs) and other aggregation-prone targets
          Challenge
          Because IDPs don't fold into a homogeneous 3D structure, you see aggregation triggered by non-native intermolecular interactions. On top of that, you are concerned with aggregation resulting from the high concentrations required by other methods.
          Solution
          With Dianthus, a high concentration is not required like it is with ITC. And if aggregation happens at low concentration, Dianthus differentiates between binding and aggregation so you get a better understanding of how the molecules behave
          Challenge
          Your method requires immobilization which easily disturbs the conformational equilibrium of IDPs.
          Solution
          Dianthus measures in solution, so the conformational equilibrium is not at risk of being disrupted as it happens with methods that require immobilization like SPR.

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