1u21

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Revision as of 17:24, 12 November 2007

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spinqualitylabelsall models 1u21, resolution 1.69Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image

transthyretin with tethered inhibitor on one monomer.

Contents 1 Overview 2 Disease 3 About this Structure 4 Reference

Overview

Protein native state stabilization imposed by small molecule binding is an, attractive strategy to prevent the misfolding and misassembly processes, associated with amyloid diseases. Transthyretin (TTR) amyloidogenesis, requires rate-limiting tetramer dissociation before misassembly of a, partially denatured monomer ensues. Selective stabilization of the native, TTR tetramer over the dissociative transition state by small molecule, binding to both thyroxine binding sites raises the kinetic barrier of, tetramer dissociation, preventing amyloidogenesis. Assessing the, amyloidogenicity of a TTR tetramer having only one amyloidogenesis, inhibitor (I) bound is challenging because the two small molecule binding, constants are generally not distinct enough to allow for the exclusive, formation of TTR.I in solution to the exclusion of TTR.I(2) and unliganded, TTR. Herein, we report a method to tether one fibril formation inhibitor, to TTR by disulfide bond formation. Occupancy of only one of the two, thyroxine binding sites is sufficient to inhibit tetramer dissociation in, 6.0 M urea and amyloidogenesis under acidic conditions by imposing kinetic, stabilization on the entire tetramer. The sufficiency of single occupancy, for stabilizing the native state of TTR provides the incentive to search, for compounds displaying striking negative binding cooperativity (e.g., K(d1) in nanomolar range and K(d2) in the micromolar to millimolar range), enabling lower doses of inhibitor to be employed in the clinic, mitigating, potential side effects.

Disease

Known diseases associated with this structure: Amyloid neuropathy, familial, several allelic types OMIM:[176300], Amyloidosis, senile systemic OMIM:[176300], Carpal tunnel syndrome, familial OMIM:[176300], Dystransthyretinemic hyperthyroxinemia OMIM:[176300]

About this Structure

1U21 is a Single protein structure of sequence from Homo sapiens with P2C as ligand. Full crystallographic information is available from OCA.

Reference

Kinetic stabilization of an oligomeric protein by a single ligand binding event., Wiseman RL, Johnson SM, Kelker MS, Foss T, Wilson IA, Kelly JW, J Am Chem Soc. 2005 Apr 20;127(15):5540-51. PMID:15826192

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