Precision measurement of ternary diffusion coefficients and implications for protein crystal growth: lysozyme chloride in aqueous ammonium chloride at 258C

نویسندگان

  • Luigi Paduano
  • Onofrio Annunziata
  • Arne J. Pearlstein
  • Donald G. Miller
  • John G. Albright
چکیده

Isothermal ternary diffusion coefficients for the system lysozyme chloride (1)+NH4Cl (2)+H2O at 258C and pH 4.5 have been measured interferometrically for five mean NH4Cl concentrations, C2 1⁄4 0:25, 0.5, 0.9, 1.2 and 1.5M, with C1 1⁄4 0:6mM. The main-term diffusion coefficient ðD11Þv varies slowly with C2. The main-term ðD22Þv increases with increasing NH4Cl concentration, as does the binary Dv in aqueous NH4Cl, but the ðD22Þv values are lower in the ternary system. The cross-term ðD21Þv, which relates the coupled flow of NH4Cl to the protein concentration gradient, increases sharply with increasing salt concentration, and is 19 times larger than ðD22Þv at the highest concentration. The values of ðD12Þv are smaller than the corresponding values previously obtained for the lysozyme chloride+NaCl+H2O system over the whole range of salt concentration studied. Using equations based on the Onsager Reciprocal Relations, we have calculated the derivative of the chemical potential of lysozyme chloride with respect to the NH4Cl concentration, and have estimated the protein cation charge. Integration with respect to the NH4Cl concentration gives the dependence of the chemical potential of lysozyme chloride on NH4Cl concentration, providing information about the driving force for nucleation and crystal growth of lysozyme chloride. # 2001 Elsevier Science B.V. All rights reserved. PACS: 36.20; 66.10; 81.10.Dn; 87.15.Da

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تاریخ انتشار 2001