Use of T4 lysozyme charge mutants to examine electrophoretic models

被引:36
作者
Durant, JA
Chen, CY
Laue, TM
Moody, TP
Allison, SA
机构
[1] Georgia State Univ, Dept Chem, Atlanta, GA 30303 USA
[2] Univ New Hampshire, Dept Biochem & Mol Biol, Ctr Advance Mol Interact Sci, Durham, NH 03824 USA
基金
美国国家科学基金会;
关键词
protein charge; electrostatic; boundary element modeling; free-solution electrophoresis; T4; lysozyme; charge mutants;
D O I
10.1016/S0301-4622(02)00168-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The electrophoretic mobility of a macro-ion is affected in a complex manner by a variety of forces that arise from the applied field. Coupling of the macro-ion and small-ion flows gives rise to non-conserved forces that are greater than those expected from ordinary hydrodynamic considerations. It is difficult to separate the steady-state hydrodynamic and electrodynamic contributions to the macro-ion mobility. Membrane-confined electrophoresis (MCE), a free solution technique, provides an experimental means by which to gain insight into these contributions. In this work we used MCE steady-state electrophoresis (SSE) of a series of T4 lysozyme charge mutants to investigate these effects and to examine the existing theoretical descriptions. These experiments isolate the effects of charge on electrophoretic mobility and permit a unique test of theories by Debye-Hilckel-Henry, Booth and Allison. Our results show that for wild type (WT) T4, where divergence is expected to be greatest, the predicted results are within 15, 8 and 1%, respectively, of experimental SSE results. Parallel experiments using another free-solution technique, capillary electrophoresis, were in good agreement with MCE results. The theoretical predictions were within 20, 13 and 5% of CE mobilities for WT. Boundary element modeling by Allison and co-workers, using continuum hydrodynamics based on detailed structural information, provides predictions in excellent agreement with experimental results at ionic strengths of 0.11 M. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:593 / 609
页数:17
相关论文
共 60 条
[1]   The length dependence of translational diffusion, free solution electrophoretic mobility, and electrophoretic tether force of rigid rod-like model duplex DNA [J].
Allison, S ;
Chen, CY ;
Stigter, D .
BIOPHYSICAL JOURNAL, 2001, 81 (05) :2558-2568
[2]   MODELING THE ELECTROPHORESIS OF RIGID POLYIONS - APPLICATION TO LYSOZYME [J].
ALLISON, SA ;
TRAN, VT .
BIOPHYSICAL JOURNAL, 1995, 68 (06) :2261-2270
[3]   Modeling the electrophoresis of rigid polyions. Inclusion of ion relaxation [J].
Allison, SA .
MACROMOLECULES, 1996, 29 (23) :7391-7401
[4]  
Allison SA, 1998, BIOPOLYMERS, V46, P359, DOI 10.1002/(SICI)1097-0282(199811)46:6<359::AID-BIP2>3.3.CO
[5]  
2-R
[6]   Modeling the electrophoresis of lysozyme .2. Inclusion of ion relaxation [J].
Allison, SA ;
Potter, M ;
McCammon, JA .
BIOPHYSICAL JOURNAL, 1997, 73 (01) :133-140
[7]   Boundary element modeling of biomolecular transport [J].
Allison, SA .
BIOPHYSICAL CHEMISTRY, 2001, 93 (2-3) :197-213
[8]   A commentary on the screened-oseen, counterion-condensation formalism of polyion electrophoresis [J].
Allison, SA ;
Stigter, D .
BIOPHYSICAL JOURNAL, 2000, 78 (01) :121-124
[9]   PH-INDUCED DENATURATION OF PROTEINS - A SINGLE SALT BRIDGE CONTRIBUTES 3-5 KCAL MOL TO THE FREE-ENERGY OF FOLDING OF T4-LYSOZYME [J].
ANDERSON, DE ;
BECKTEL, WJ ;
DAHLQUIST, FW .
BIOCHEMISTRY, 1990, 29 (09) :2403-2408
[10]  
ANDERSON DE, 1992, THESIS U OREGON EUGE