44 research outputs found
Palaeomagnetism of three dyke swarms in Nansen Land, north Greenland (83° N)
Three basic dyke swarms of post-Ellesmerian (post-Early Carboniferous) age in Nansen Land (83° N, 43° W) are still not dated numerically, but cross-cutting relationships show Group 1 to be older than Group 2, while Group 3 is the freshest and likely the youngest. Group 1 (the most northerly swarm) strikes N-S; Group 2 NW-SE, and Group 3 (the most southerly swarm) E-W. From more than 200 dykes 234 specimens from 28 sites were investigated palaeomagnetically. Group 1 dykes show unexpected shallow inclinations with a cleaned mean direction of (Dm, Im) = (151°, −5.8°), N = 7, k = 18.5, α 95 = 13.9°. They show hydrothermal alterations, some remagnetization by lightning, and the low inclination indicates a low palaeo latitude. The palaeopole is (Plat, Plon) = (8.9° S, 14.0° W) with (dp, dm) = (7°, 14°), and is close to the North American Early Carboniferous mean pole, suggesting a syn- or early late-tectonic dyke injection. The polarity is reverse. Groups 2 and 3 of presumed Cretaceous or Tertiary age show dominantly normal and reverse polarities, respectively. Their mean directions per polarity are well grouped, with (Dm, Im) = (−30.6°, 76.7°), n = 13, k = 191.4, α 95 = 3.9°, and (Dm, Im) = (133.4°, −76.7°), n = 10, k = 87.5, α 95 = 5.9°, respectively. They are antipodal within 95% significance, and combining both swarms gives (Dm, Im) = (−37.5°, 76.8°), n = 23, k = 124.3, α 95 = 2.7°, corresponding to a mean pole of (Plat, Plon) = (70.0° N, 185.1° E) with (dp, dm) = (4.7°, 5.0°), for which the spline of Late Cretaceous-Tertiary poles for all Greenland indicates a palaeomagnetic age of 57 ± 10 Ma. This pole (in present-day coordinates) is very close to the Late Cretaceous North American pole, in accordance with the fact that Greenland belongs to the North American craton, and that the two younger swarms are essentially postdating the opening of Baffin Bay.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/43921/1/11288_2004_Article_147530.pd
U–Pb geochronology of Neoproterozoic and Caledonian tectonothermal events in the East Greenland Caledonides
SHRIMP U-Pb geochronology and metamorphic history of the Smallefjord sequence, NE Greenland Caledonides
Regional Caledonian structure within an oblique convergence zone, Dronning Louise Land, NE Greenland
Lithostratigraphic framework of the Upper Proterozoic and Lower Paleozoic deep water clastic deposits of North Greenland
Ligand-Controlled Assembly of Hexamers, Dihexamers, and Linear Multihexamer Structures by the Engineered Acylated Insulin Degludec
Insulin degludec, an engineered acylated insulin, was recently reported to form a soluble depot after subcutaneous injection with a subsequent slow release of insulin and an ultralong glucose-lowering effect in excess of 40 h in humans. We describe the structure, ligand binding properties, and self-assemblies of insulin degludec using orthogonal structural methods. The protein fold adopted by insulin degludec is very similar to that of human insulin. Hexamers in the R(6) state similar to those of human insulin are observed for insulin degludec in the presence of zinc and resorcinol. However, under conditions comparable to the pharmaceutical formulation comprising zinc and phenol, insulin degludec forms finite dihexamers that are composed of hexamers in the T(3)R(3) state that interact to form an R(3)T(3)-T(3)R(3) structure. When the phenolic ligand is depleted and the solvent condition thereby mimics that of the injection site, the quaternary structure changes from dihexamers to a supramolecular structure composed of linear arrays of hundreds of hexamers in the T(6) state and an average molar mass, M(0), of 59.7 × 10(3) kg/mol. This novel concept of self-assemblies of insulin controlled by zinc and phenol provides the basis for the slow action profile of insulin degludec. To the best of our knowledge, this report for the first time describes a tight linkage between quaternary insulin structures of hexamers, dihexamers, and multihexamers and their allosteric state and its origin in the inherent propensity of the insulin hexamer for allosteric half-site reactivity