Advances in Chemical Physics, Volume 155 by Stuart A. Rice, Aaron R. Dinner PDF

By Stuart A. Rice, Aaron R. Dinner

ISBN-10: 1118755774

ISBN-13: 9781118755778

Every one quantity of the Advances in Chemical Physics sequence discusses facets of the country of various matters in chemical physics and similar fields, with chapters written by way of most sensible researchers within the box. reports released in Advances in Chemical Physics are usually longer than these released in journals, supplying the distance wanted for readers to completely seize the subject, together with basics, most modern discoveries, purposes, and rising avenues of research.

Volume one hundred fifty five explores:
• Modeling viral capsid assembly
• fees at aqueous interfaces, together with the advance of computational ways in direct touch with the experiment
• conception and simulation advances in solute precipitate nucleation
• A computational standpoint of water within the liquid state
• building of strength capabilities for lattice heteropolymer types, together with effective encodings for constraint pride programming and quantum annealing

Advances in Chemical Physics is perfect for introducing newbies to subject matters in chemical physics and serves because the excellent complement to any complex graduate category dedicated to its research. The sequence additionally offers the root wanted for more matured researchers to develop examine experiences.

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Extra resources for Advances in Chemical Physics, Volume 155

Example text

However, for much of parameter space the system reaches an outcome that is nearly stationary with respect to experimentally relevant timescales due to the fact that bond breaking is an activated process. 34 Reduced temperature, T* MICHAEL F. 5 Capsomer concentration (In[c]) 5 Figure 15. , inverse of interaction strength) and particle concentration. Representative structures are shown for the well-formed and misassembled regions. Figure adapted with permission from Ref. [151], copyright (2007) American Chemical Society.

These peptide tails are commonly referred to as arginine-rich motifs (ARMs). A remarkable set of in vitro experiments indicates that just the negative charge found on the RNA phosphate groups is sufficient to drive ssRNA capsid assembly around a cargo. , [85,201,217,229,237--242]), synthetic polyelectrolytes [230,238,240,243--248], charge-functionalized nanoparticles [203,204,249--253], DNA micelles [254], and nanoemulsions [255]. However, as discussed further below, features specific to biological RNA molecules such as their tertiary structure and sequence-specific interactions likely promote selective assembly around the viral genome or help direct assembly toward particular morphologies.

Hicks and Henley [150] proposed a model for assembly of HIV capsids in which triangular subunits were irreversibly attached to sites on a growing cluster according to the local geometry to form hexagonal or pentagonal substructures, with a subunit--subunit interaction geometry that defined a preferred spontaneous curvature. They found that under irreversible attachment the model produced an ensemble of irregular structures, but not the conical shells observed in EM images of mature HIV capsids [60,61].

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Advances in Chemical Physics, Volume 155 by Stuart A. Rice, Aaron R. Dinner


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