• Zum Seiteninhalt (Accesskey 1)
  • Zur Hauptnavigation (Accesskey 2)
  • Bundesministerium Frauen, Wissenschaft und Forschung
  • Forschungsinfrastruktur-Datenbank
  • Start
  • Search
  • Mapping
    • Statistics by region
    • Cluster
    • Monitoring
    • ESFRI-AT-Mapping
    • Gallery
  • About
  • FAQs & Info
    • FAQs
      • Description of the Research Infrastructure
      • Methods & Services for Research Infrastructure
      • Research infrastructure categories
      • Additional Information to research Infrastructure
      • Search Engine
      • Contact
    • Information
      • National Strategy of Research Infrastructure
      • Research infrastructures in the European Union
      • Research infrastructure databases / Research infrastructure networks
      • BMBWF Research Infrastructure Database: Evaluation Study 2022
      • Awards and press releases
  • Registrieren
  • Login
  • DE
  • EN
Large equipment

Monolith Pico Red

  • To Overview
  • »
  • 92 / 1160
  • »

University of Veterinary Medicine Vienna

Wien | Website

Open for Collaboration

Short Description

The NanoTemper Monolith Pico Red is a MicroScale Thermophoresis (MST)-based instrument designed to quantify biomolecular interactions in solution under near-native conditions. It enables the rapid determination of binding affinities across a broad dynamic range of picomolar to millimolar concentrations. MST is a technique for measuring the movement of molecules in a temperature gradient, known as thermophoresis, which depends on the magnitude of the charge and the hydration shell of the molecules. When a molecule is exposed to a temperature gradient, it moves toward cooler or warmer regions depending on its properties, and this movement can be detected by observing the change in fluorescence of a labeled molecule.

In MST, a fluorescently labeled target molecule is exposed to a temperature gradient, and the change in its migration pattern is tracked in real time. When a ligand binds to the target molecule, it alters its thermophoretic behavior, leading to a measurable shift in the fluorescence signal. This enables the determination of binding affinity, stoichiometry, and the kinetics of molecular interactions without the need for complex labeling or surface immobilization.

Contact Person

Sebastian Glatt

Research Services

MicroScale Thermophoresis (MST), RNA and Protein Interaction Assays

Methods & Expertise for Research Infrastructure

MST is a technique for measuring the movement of molecules in a temperature gradient, known as thermophoresis, which depends on the magnitude of the charge and the hydration shell of the molecules.

Terms of Use

Inquiries directly by phone or email

Reference Publications

RNA-triggered Cas12a3 cleaves tRNA tails to execute bacterial immunity.
Dmytrenko O, Yuan B, Crosby KT, Krebel M, Chen X, Nowak JS, Chramiec-Głąbik A, Filani B, Gribling-Burrer AS, van der Toorn W, von Kleist M, Achmedov T, Smyth RP, Glatt S, Bravo JPK, Heinz DW, Jackson RN, Beisel CL.
Nature. 2026 Jan;649(8099):1312-1321. doi: 10.1038/s41586-025-09852-9. Epub 2026 Jan 7.
PMID: 41501459
https://www.nature.com/articles/s41586-025-09852-9

Queuosine is incorporated into precursor tRNA before splicing.
Guo W, Kaczmarczyk I, Kopietz K, Flegler F, Russo S, Cigirgan E, Chramiec-Głąbik A, Koziej Ł, Cirzi C, Peschek J, Reuter K, Helm M, Glatt S, Tuorto F.
Nat Commun. 2025 Jul 31;16(1):7044. doi: 10.1038/s41467-025-62220-z.
PMID: 40745156
https://www.nature.com/articles/s41467-025-62220-z

Structural and biochemical characterization of the 3'-5' tRNA splicing ligases.
Chamera S, Zajko W, Czarnocki-Cieciura M, Jaciuk M, Koziej Ł, Nowak J, Wycisk K, Sroka M, Chramiec-Głąbik A, Śmietański M, Gołębiowski F, Warmiński M, Jemielity J, Glatt S, Nowotny M.
J Biol Chem. 2025 May;301(5):108506. doi: 10.1016/j.jbc.2025.108506. Epub 2025 Apr 10.
PMID: 40220997
https://linkinghub.elsevier.com/retrieve/pii/S0021-92582500355-2

The molecular basis of tRNA selectivity by human pseudouridine synthase 3.
Lin TY, Kleemann L, Jeżowski J, Dobosz D, Rawski M, Indyka P, Ważny G, Mehta R, Chramiec-Głąbik A, Koziej Ł, Ranff T, Fufezan C, Wawro M, Kochan J, Bereta J, Leidel SA, Glatt S.
Mol Cell. 2024 Jul 11;84(13):2472-2489.e8. doi: 10.1016/j.molcel.2024.06.013.
PMID: 38996458
https://linkinghub.elsevier.com/retrieve/pii/S1097-27652400520-3

Contact

Sebastian Glatt ist Professor für Systemgenetik an der Veterinärmedizinischen Universität Wien
Sebastian Glatt
Department for Biological Sciences and Pathobiology
+43 1 25077-5622
sebastian.glatt@vetmeduni.ac.at
https://www.vetmeduni.ac.at/tierzucht/systemgenetik
https://www.vetmeduni.ac.at

Location

Location on map

Share this entry

  • Facebook
  • X.com
  • Pinterest
  • LinkedIn
  • E-Mail
© 2026 FEDERAL MINISTRY of WOMEN, SCIENCE and RESEARCH
  • Terms of use / General Data Protection Regulation
  • Declaration on accessibility
  • Imprint
  • Data protection settings