NMR paper Drug Screening Boosted by Hyperpolarized Long-Lived States in NMR.

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[NMR paper] Drug Screening Boosted by Hyperpolarized Long-Lived States in NMR.

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Amber

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Fragment-based:

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TALOS

Promega- Proline

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CSI (via RCI server)

TALOS

MICS caps, β-turns

d2D

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09-10-2014, 11:24 AM

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Drug Screening Boosted by Hyperpolarized Long-Lived States in NMR.

Drug Screening Boosted by Hyperpolarized Long-Lived States in NMR.

Related Articles Drug Screening Boosted by Hyperpolarized Long-Lived States in NMR.

ChemMedChem. 2014 Sep 4;

Authors: Buratto R, Bornet A, Milani J, Mammoli D, Vuichoud B, Salvi N, Singh M, Laguerre A, Passemard S, Gerber-Lemaire S, Jannin S, Bodenhausen G

Abstract
Transverse and longitudinal relaxation times (T1? and T1 ) have been widely exploited in NMR to probe the binding of ligands and putative drugs to target proteins. We have shown recently that long-lived states (LLS) can be more sensitive to ligand binding. LLS can be excited if the ligand comprises at least two coupled spins. Herein we broaden the scope of ligand screening by LLS to arbitrary ligands by covalent attachment of a functional group, which comprises a pair of coupled protons that are isolated from neighboring magnetic nuclei. The resulting functionalized ligands have longitudinal relaxation times T1 ((1) H) that are sufficiently long to allow the powerful combination of LLS with dissolution dynamic nuclear polarization (D-DNP). Hyperpolarized weak "spy ligands" can be displaced by high-affinity competitors. Hyperpolarized LLS allow one to decrease both protein and ligand concentrations to micromolar levels and to significantly increase sample throughput.

PMID: 25196781 [PubMed - as supplied by publisher]

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