19 research outputs found
Against all odds? Forming the planet of the HD196885 binary
HD196885Ab is the most "extreme" planet-in-a-binary discovered to date, whose
orbit places it at the limit for orbital stability. The presence of a planet in
such a highly perturbed region poses a clear challenge to planet-formation
scenarios. We investigate this issue by focusing on the planet-formation stage
that is arguably the most sensitive to binary perturbations: the mutual
accretion of kilometre-sized planetesimals. To this effect we numerically
estimate the impact velocities amongst a population of circumprimary
planetesimals. We find that most of the circumprimary disc is strongly hostile
to planetesimal accretion, especially the region around 2.6AU (the planet's
location) where binary perturbations induce planetesimal-shattering of
more than 1km/s. Possible solutions to the paradox of having a planet in such
accretion-hostile regions are 1) that initial planetesimals were very big, at
least 250km, 2) that the binary had an initial orbit at least twice the present
one, and was later compacted due to early stellar encounters, 3) that
planetesimals did not grow by mutual impacts but by sweeping of dust (the
"snowball" growth mode identified by Xie et al., 2010b), or 4) that HD196885Ab
was formed not by core-accretion but by the concurent disc instability
mechanism. All of these 4 scenarios remain however highly conjectural.Comment: accepted for publication by Celestial Mechanics and Dynamical
Astronomy (Special issue on EXOPLANETS
Hydrophobic and ionic-interactions in bulk and confined water with implications for collapse and folding of proteins
Water and water-mediated interactions determine thermodynamic and kinetics of
protein folding, protein aggregation and self-assembly in confined spaces. To
obtain insights into the role of water in the context of folding problems, we
describe computer simulations of a few related model systems. The dynamics of
collapse of eicosane shows that upon expulsion of water the linear hydrocarbon
chain adopts an ordered helical hairpin structure with 1.5 turns. The structure
of dimer of eicosane molecules has two well ordered helical hairpins that are
stacked perpendicular to each other. As a prelude to studying folding in
confined spaces we used simulations to understand changes in hydrophobic and
ionic interactions in nano droplets. Solvation of hydrophobic and charged
species change drastically in nano water droplets. Hydrophobic species are
localized at the boundary. The tendency of ions to be at the boundary where
water density is low increases as the charge density decreases. Interaction
between hydrophobic, polar, and charged residue are also profoundly altered in
confined spaces. Using the results of computer simulations and accounting for
loss of chain entropy upon confinement we argue and then demonstrate, using
simulations in explicit water, that ordered states of generic amphiphilic
peptide sequences should be stabilized in cylindrical nanopores