Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

High-throughput screening: advances in assay technologies

G S Sittampalam1, S D Kahl, W P Janzen

  • 1Research Technologies and Proteins, Lilly Research Laboratories, Eli Lilly and Company Indianapolis, Indiana, 46285, USA. sitta@lilly.com

Current Opinion in Chemical Biology
|July 17, 1998
PubMed
Summary

High-throughput screening (HTS) uses isotopic and nonisotopic assays for drug discovery. Advances focus on automated, homogenous assay systems and cell-based screens to identify drug candidates efficiently.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

High-throughput screening identifies small molecules that enhance the pharmacological effects of oligonucleotides.

Nucleic acids research·2015
Same author

Differential distribution of urocortin- and corticotropin-releasing factor-like immunoreactivities in the rat brain.

Neuroscience·1999
Same author

BOCILLIN FL, a sensitive and commercially available reagent for detection of penicillin-binding proteins.

Antimicrobial agents and chemotherapy·1999
Same author

Conceptual and statistical issues in the validation of analytic dilution assays for pharmaceutical applications.

Journal of biopharmaceutical statistics·1998
Same author

Characterization of [125I-Tyr0]-corticotropin releasing factor (CRF) binding to the CRF binding protein using a scintillation proximity assay.

Journal of neuroscience methods·1998
Same author

Synthesis and characterization of insulin-fluorescein derivatives for bioanalytical applications.

Analytical chemistry·1998

Area of Science:

  • Biochemistry
  • Pharmacology
  • Drug Discovery

Background:

  • High-throughput screening (HTS) is crucial for identifying novel drug candidates.
  • Assay methodologies, including isotopic and nonisotopic approaches, are fundamental to HTS.
  • Recent technological advancements are enhancing the efficiency and scope of HTS.

Purpose of the Study:

  • To review recent advances in cell-based and in vitro biochemical assays for drug discovery.
  • To highlight detection technologies suitable for automated 'mix and read' procedures in HTS.
  • To discuss emerging trends in HTS assay development.

Main Methods:

  • Review of recent literature on assay methodologies in HTS.
  • Emphasis on homogenous assay systems utilizing fluorescence resonance energy transfer (FRET), fluorescence polarization (FP), and fluorescence correlation spectroscopy (FCS).

Related Experiment Videos

  • Discussion of cell-based assay systems and their application in identifying disease-target modulating compounds.
  • Main Results:

    • Homogenous assay systems employing FRET, FP, and FCS represent a major trend in HTS.
    • Cell-based assays are increasingly utilized to identify compounds that directly modulate disease targets.
    • Colorimetric and amperometric methods show potential but are not yet widely adopted in HTS.

    Conclusions:

    • Advancements in assay technologies are significantly improving drug discovery through HTS.
    • Homogenous and cell-based assay systems offer powerful tools for efficient identification of active compounds.
    • Continued development of detection technologies will further optimize HTS processes.