SPEC PerkinElmer 10.13

Biological, Medical, and Clinical Analysis

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Using a new mass spectrometry technique and stem cells that can be made to produce either neurons or glial cells, a team of researchers at the Salk Institute for Biological Studies (La Jolla, California) identified a molecular signaling pathway that is required for the production of glial cells, yielding insight into the neurobiology of Down?s syndrome and several nervous system disorders characterized by too many glial cells.

Spectroscopy

January 2007. This review article summarizes biological applications that utilize surface plasmon resonance, localized surface plasmon resonance, and surface-enhanced Raman spectroscopy.

Spectroscopy

The concentration dependent influence of Na+ and K+ions on mass spectra of peptides is shown with human gastrin as a model peptide. With electrospray ionization the doubly charged protonated molecule ion [M+2H]2+ is normally the preferred ionization product. However, trace amounts of alkali metal ions already form clusters (adducts) with the peptide molecule, such as [M+H+Na]2+, which become dominating at higher concentrations. With Na+/K+ concentrations below 0.1 mg/kg (ppm) only a few clusters appear, which allow the correct doubly charged molecule ion to be assigned for a subsequent MS–MS experiment. With concentrations of 10 ppm and higher the alkali clusters become the most abundant peaks in the spectrum, and the absolute sensitivity is decreased by a factor of 5–10. Experiments were performed with water and water–methanol mixtures with a known Na+/K+ +content.

Spectroscopy

Many important biological signals are triggered by the binding of a peptide hormone to its cognate receptor at the cell surface. Using stopped-flow fluorescence spectroscopy, the authors have been able to observe, in real time, ligand binding to epidermal growth factor receptors expressed at the surface of intact cells. This method allows for the measurement of kinetic association and dissociation rates with high data density in a native cellular environment, providing insights into the signal-initiation process in this system that have not been revealed through the determination of ligand-binding constants obtained by more traditional methods.