4.8 Article

Single-stranded nucleic acid elasticity arises from internal electrostatic tension

出版社

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1701132114

关键词

single-stranded nucleic acids; flexible polyelectrolytes; force spectroscopy; electrostatics

资金

  1. National Science Foundation (NSF) [DMR-1309414]
  2. NSF [DGE-1144085, DMR-1309892, DMR-1436201, DMR-1121107]
  3. National Institutes of Health [P01-HL108808, 1UH2HL123645]
  4. Cystic Fibrosis Foundation
  5. US Department of Energy's National Nuclear Security Administration [DE-AC04-94AL85000]
  6. Direct For Mathematical & Physical Scien
  7. Division Of Materials Research [1309892, 1309414] Funding Source: National Science Foundation

向作者/读者索取更多资源

Understanding of the conformational ensemble of flexible polyelectrolytes, such as single-stranded nucleic acids (ssNAs), is complicated by the interplay of chain backbone entropy and salt-dependent electrostatic repulsions. Molecular elasticity measurements are sensitive probes of the statistical conformation of polymers and have elucidated ssNA conformation at low force, where electrostatic repulsion leads to a strong excluded volume effect, and at high force, where details of the backbone structure become important. Here, we report measurements of ssDNA and ssRNA elasticity in the intermediate-force regime, corresponding to 5- to 100-pN forces and 50-85% extension. These data are explained by a modified wormlike chain model incorporating an internal electrostatic tension. Fits to the elastic data show that the internal tension decreases with salt, from >5 pN under 5 mM ionic strength to near zero at 1 M. This decrease is quantitatively described by an analytical model of electrostatic screening that ascribes to the polymer an effective charge density that is independent of force and salt. Our results thus connect microscopic chain physics to elasticity and structure at intermediate scales and provide a framework for understanding flexible polyelectrolyte elasticity across a broad range of relative extensions.

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