Force spectroscopy of hyaluronan by atomic force microscopy: from hydrogen-bonded networks toward single-chain behavior

Biomacromolecules. 2007 Sep;8(9):2648-52. doi: 10.1021/bm700592j. Epub 2007 Aug 1.

Abstract

The conformational behavior of hyaluronan (HA) polysaccharide chains in aqueous NaCl solution was characterized directly at the single-molecule level. This communication reports on one of the first single-chain atomic force microscopy (AFM) experiments performed at variable temperatures, investigating the influence of the temperature on the stability of the HA single-chain conformation. Through AFM single-molecule force spectroscopy, the temperature destabilization of a local structure was proven. This structure involved a hydrogen-bonded network along the polymeric chain, with hydrogen bonds between the polar groups of HA and possibly water, and a change from a nonrandom coil to a random coil behavior was observed when increasing the temperature from 29 +/- 1 to 46 +/- 1 degrees C. As a result of the applied force, this superstructure was found to break progressively at room temperature. The use of a hydrogen-bonding breaker solvent demonstrated the hydrogen-bonded water-bridged nature of the network structure of HA single chains in aqueous NaCl solution.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Hyaluronic Acid / chemistry*
  • Hydrogen Bonding*
  • Microscopy, Atomic Force*
  • Molecular Structure
  • Spectrum Analysis*

Substances

  • Hyaluronic Acid