Highly permeable polymeric membranes based on the incorporation of the functional water channel protein Aquaporin Z

  1. Manish Kumar*,
  2. Mariusz Grzelakowski,
  3. Julie Zilles*,
  4. Mark Clark*, and
  5. Wolfgang Meier,
  1. *Department of Civil and Environmental Engineering, University of Illinois at Urbana–Champaign, 205 North Mathews Avenue, Urbana, IL 61801; and
  2. Department of Chemistry, University of Basel, Klingelbergstrasse 80, CH-4056 Basel, Switzerland
  1. Edited by Nicholas J. Turro, Columbia University, New York, NY, and approved October 30, 2007 (received for review September 15, 2007)

Abstract

The permeability and solute transport characteristics of amphiphilic triblock-polymer vesicles containing the bacterial water-channel protein Aquaporin Z (AqpZ) were investigated. The vesicles were made of a block copolymer with symmetric poly-(2-methyloxazoline)-poly-(dimethylsiloxane)-poly-(2-methyloxazoline) (PMOXA15-PDMS110-PMOXA15) repeat units. Light-scattering measurements on pure polymer vesicles subject to an outwardly directed salt gradient in a stopped-flow apparatus indicated that the polymer vesicles were highly impermeable. However, a large enhancement in water productivity (permeability per unit driving force) of up to ≈800 times that of pure polymer was observed when AqpZ was incorporated. The activation energy (E a) of water transport for the protein-polymer vesicles (3.4 kcal/mol) corresponded to that reported for water-channel-mediated water transport in lipid membranes. The solute reflection coefficients of glucose, glycerol, salt, and urea were also calculated, and indicated that these solutes are completely rejected. The productivity of AqpZ-incorporated polymer membranes was at least an order of magnitude larger than values for existing salt-rejecting polymeric membranes. The approach followed here may lead to more productive and sustainable water treatment membranes, whereas the variable levels of permeability obtained with different concentrations of AqpZ may provide a key property for drug delivery applications.

Footnotes

  • To whom correspondence should be addressed. E-mail: wolfgang.meier{at}unibas.ch
  • Author contributions: M.K., J.Z., M.C., and W.M. designed research; M.K., M.G., and J.Z. performed research; M.K. and M.G. analyzed data; and M.K., J.Z., M.C., and W.M. wrote the paper.

  • The authors declare no conflict of interest.

  • This article is a PNAS Direct Submission.

  • See Commentary on page 20643.

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