New Mexico Molecular Libraries Screening Center


New Mexico Molecular Libraries Screening Center

Principal Investigator: Larry Sklar

The New Mexico Molecular Libraries Screening Center has developed innovative flow cytometric tools for discovery research that enable homogeneous analysis of ligand binding and protein-protein interaction, HT sample handling, high content analysis, and real-time measurements of cell response. Our experience indicates that virtually any molecular assembly or cell response can be displayed in a format compatible with flow cytometry. Moreover, by creating a suspension array of particles, assays and responses can be highly multiplexed or performed on complex cell populations without loss of throughput. Our novel sampling approach (HyperCyt ?) makes flow cytometry an attractive platform for drug discovery, proteomics, and real-time analysis of molecular interactions. Flow cytometry is particularly convenient for alternately assessing both cellular and molecular activities of small molecules. To our knowledge, there is no single competing technology that offers the versatility of flow cytometry for Molecular Library Initiative screening or that has the potential of being available to such a large number of laboratories that house flow cytometers (20,000 world-wide). Our team brings together expertise that spans biomedical, biophysical, chemical, computational, instrumentation and engineering disciplines. We are particularly interested in enhancing the overall discovery process through the integration of physical screening and computational tools that include virtual screening, cheminformatics, and data mining.

New Mexico Capabilities and Technologies

Assay Formats Screening Capabilities Biologicial Expertise
High-throughput flow cytometry Cell-based Assays Protein-protein interactions
Solution and Suspension based absorbance, fluorescence steady-state and lifetime Bead-based Assays Protein-nucleic acid interactions
Fluorescence and phase-contrast microscopy Informatics (virtual screening, clustering and in silico profiling) Kinase assays
Plate Based fluorescence, absorbance, polarization, and luminescence Multiparametric high content analysis GPCRs
  Multiparametric multiplex analysis Integrins and adhesion molecules
  High throughput analysis of compound solubility Proteases/proteasome
  High Throughput and Multiparametric analysis of compound fluorescence (3 colors of excitation, 9 colors of emission) Cell cycle
    Apoptosis
     

For inquiries about assay development at a particular The New Mexico Molecular Libraries Screening Center, please contact the center representative listed in conjunction with visiting the Center’s Web site.

See also: Enabling PI-Center Collaboration Document