IONIC-STRENGTH-DEPENDENT AND PH-DEPENDENT CONFORMATIONAL STATES OF HUMAN PLASMA FIBRONECTIN

被引:27
作者
BENECKY, MJ
WINE, RW
KOLVENBACH, CG
MOSESSON, MW
机构
[1] Sinai Samaritan Medical Center, University of Wisconsin Medical School, Milwaukee Clinical Campus, Milwaukee
[2] Amgen Corporation, Thousand Oaks, CA 91320
关键词
D O I
10.1021/bi00231a028
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
In order to provide a more detailed understanding of human plasma fibronectin (PFn) solution structure, we examined the effects of pH and ionic strength (mu) variation on the sedimentation velocities (s20,w), fluorescence polarization-derived mean harmonic rotational relaxation times (rho-H), far-ultraviolet (UV) circular dichroism (CD), and intrinsic tryptophan fluorescence of dimeric PFn and the monomeric 190/170-kDa PFn fragment. By comparing the biophysicial properties of PFn with those of the 190/170-kDa PFn fragment, we could assess the relative importance of intrasubunit and intersubunit electrostatic forces in the stabilization of PFn structure. The rho-H derived from isothermal polarization measurements on 1-pyrenebutyrate conjugated PFn decreased markedly (4.5 --> 1.05-1.23-mu-s) when mu was increased from 0.2 to 1.2 or when the pH was adjusted from 7.4 to 2.0 or 11.0. We also noted a significant decrease in the PFn s20,W (13 --> 8.5-9.6S) under these same solvent conditions. In contrast, the rho-H and s20,W of the monomeric 190/170-kDa PFn fragment were relatively insensitive to changes in mu or pH. Computer simulations of the observed pH-dependent changes in the far-UV CD of PFn and the 190/170-kDa PFn fragment revealed only minor differences in protein secondary structure. We also observed only small bathochromic shifts (1-3 nm) in the emission maxima of PFn and 190/170-kDa PFn fragment tryptophan fluorescence under acidic or high mu conditions. These results suggest that minimal changes in PFn tertiary (i.e., intrasubunit) structure occur at pH 2, 11, or at mu = 1.2. We therefore conclude that the driving force behind the observed pH- and mu-induced conformational changes in PFn is disruption of intersubunit electrostatic contacts. Our data suggest that the "unfolded" PFn conformation occurring at pH 2, 11, or mu = 1.2 can be approximated by a structure consisting of two independently rotating disk-shaped subunits, each having a diameter and thickness of 20 and 2.3 nm, respectively.
引用
收藏
页码:4298 / 4306
页数:9
相关论文
共 55 条
[1]   PROTEIN-STRUCTURE PROBED BY POLARIZATION SPECTROSCOPY .2. A TIME-RESOLVED FLUORESCENCE STUDY OF HUMAN-FIBRINOGEN [J].
ACUNA, AU ;
GONZALEZRODRIGUEZ, J ;
LILLO, MP ;
NAQVI, KR .
BIOPHYSICAL CHEMISTRY, 1987, 26 (01) :63-70
[2]  
ALEXANDER SS, 1979, J BIOL CHEM, V254, P1501
[3]   HEPARIN MODULATES CONFORMATIONAL STATES OF PLASMA FIBRONECTIN - AN ELECTRON-SPIN-RESONANCE SPIN LABEL APPROACH [J].
ANKEL, EG ;
HOMANDBERG, G ;
TOONEY, NM ;
LAI, CS .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1986, 244 (01) :50-56
[4]   HUMAN PLASMA FIBRONECTIN STRUCTURE PROBED BY STEADY-STATE FLUORESCENCE POLARIZATION - EVIDENCE FOR A RIGID OBLATE STRUCTURE [J].
BENECKY, MJ ;
KOLVENBACH, CG ;
WINE, RW ;
DIORIO, JP ;
MOSESSON, MW .
BIOCHEMISTRY, 1990, 29 (12) :3082-3091
[5]   EVIDENCE THAT BINDING TO THE CARBOXYL-TERMINAL HEPARIN-BINDING DOMAIN (HEP-II) DOMINATES THE INTERACTION BETWEEN PLASMA FIBRONECTIN AND HEPARIN [J].
BENECKY, MJ ;
KOLVENBACH, CG ;
AMRANI, DL ;
MOSESSON, MW .
BIOCHEMISTRY, 1988, 27 (19) :7565-7571
[6]   MEASUREMENT OF DECLINE OF FLUORESCENT ANISOTROPY OF GAMMA-GLOBULIN AND FAB, FE AND F(AB)2 FRAGMENTS LABELED WITH 1-SULFONYL-5-DIMETHYLAMINONAPHTHALENE [J].
BROCHON, JC ;
WAHL, P .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1972, 25 (01) :20-&
[7]  
Cantor C. R., 1980, BIOPHYSICAL CHEM 2, P560
[8]   HETEROGENEITY OF COLD-INSOLUBLE GLOBULIN OF HUMAN-PLASMA (CIG), A CIRCULATING CELL-SURFACE PROTEIN [J].
CHEN, AB ;
AMRANI, DL ;
MOSESSON, MW .
BIOCHIMICA ET BIOPHYSICA ACTA, 1977, 493 (02) :310-322
[9]   DOMAIN-STRUCTURE OF HUMAN-PLASMA AND CELLULAR FIBRONECTIN - USE OF A MONOCLONAL-ANTIBODY AND HEPARIN AFFINITY TO IDENTIFY 3 DIFFERENT SUBUNIT CHAINS [J].
CLICK, EM ;
BALIAN, G .
BIOCHEMISTRY, 1985, 24 (23) :6685-6696
[10]   SHAPES, DOMAIN ORGANIZATIONS AND FLEXIBILITY OF LAMININ AND FIBRONECTIN, 2 MULTIFUNCTIONAL PROTEINS OF THE EXTRACELLULAR-MATRIX [J].
ENGEL, J ;
ODERMATT, E ;
ENGEL, A ;
MADRI, JA ;
FURTHMAYR, H ;
ROHDE, H ;
TIMPL, R .
JOURNAL OF MOLECULAR BIOLOGY, 1981, 150 (01) :97-120