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Arthur McClelland

Publications and source records attributed to Arthur McClelland.

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Fossil and present-day stromatolite ooids contain a meteoritic polymer of glycine and iron

Hemoglycin, a space polymer of glycine and iron, has been identified in the carbonaceous chondritic meteorites Allende, Acfer 086, Kaba, Sutters Mill and Orgueil. Its core form has a mass of 1494Da and is basically an antiparallel pair of polyglycine strands linked at each end by an iron atom. The polymer forms two- and three- dimensional lattices with an inter-vertex distance of 4.9nm. Here the extraction technique for meteorites is applied to a 2.1Gya fossil stromatolite to reveal the presence of hemoglycin by mass spectrometry. Intact ooids from a recent (3,000Ya) stromatolite exhibited the same visible hemoglycin fluorescence in response to x-rays as an intact crystal from the Orgueil meteorite. X-ray analysis confirmed the existence in ooids of an internal 3-dimensional lattice of 4.9nm inter-vertex spacing, matching the spacing of lattices in meteoritic crystals. FTIR measurements of acid-treated ooid and a Sutters Mill meteoritic crystal both show the presence, via the splitting of the Amide I band, of an extended anti-parallel beta sheet structure. It seems probable that the copious in-fall of carbonaceous meteoritic material, from Archaean times onward, has left traces of hemoglycin in sedimentary carbonates and potentially has influenced ooid formation.

physics.geo-ph

A native chemical chaperone in the human eye lens

Cataract is one of the most prevalent protein aggregation disorders and still the biggest cause of vision loss worldwide. The human lens, in its core region, lacks turnover of any cells or cellular components; it has therefore evolved remarkable mechanisms for resisting protein aggregation for a lifetime. We now report that one such mechanism relies on an unusually abundant metabolite, myo-inositol, to suppress light-scattering aggregation of lens proteins. We quantified aggregation suppression by in vitro turbidimetry and characterized both macroscopic and microscopic mechanisms of myo-inositol action using negative-stain electron microscopy, differential scanning fluorometry, and a thermal scanning Raman spectroscopy apparatus. Given recent metabolomic evidence that it is dramatically depleted in human cataractous lenses compared to age-matched controls, we suggest that maintaining or restoring healthy levels of myo-inositol in the lens may be a simple, safe, and widely available strategy for reducing the global burden of cataract.

q-bio.BM