Experimental evidence for multiple assembled states of Sc3 from Schizophyllum commune

被引:19
作者
Stroud, PA
Goodwin, JS
Butko, P
Cannon, GC
McCormick, CL
机构
[1] Univ So Mississippi, Dept Polymer Sci, Hattiesburg, MS 39406 USA
[2] Univ So Mississippi, Dept Chem & Biochem, Hattiesburg, MS 39406 USA
关键词
D O I
10.1021/bm034045e
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 hydrophobin Sc3 from the fungus Schizophyllum commune assembles from the aqueous phase into ordered structures with substantially different characteristics depending upon experimental conditions. Under the first condition, a vortexing procedure widely reported in the literature, interfacial assembly yields highly ordered, stacked beta-sheets. We have also observed a previously unreported assembly of Sc3 under a second condition, which occurs in a time-dependent manner from quiescent solution. The resulting types of assembled states have been compared utilizing fluorescence techniques, sodium dodecyl sulfate polyacrylamide gel electrophoresis, immunoblotting, density gradient centrifugation, and phase contrast and atomic force microscopy. A model based on this study and previous literature is proposed that suggests three distinct states of Sc3: (1) soluble Sc3 consisting of unimers or multimers. in micelle-like association, (2) interfacially assembled I-Sc3 with highly ordered, stacked beta-sheets, presumably formed in a templated manner at the air/water interface of microscopic bubbles generated by vortexing, and (3) solution-assembled S-Sc3, a less-ordered structure formed in a time-dependent manner in the absence of an interface.
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收藏
页码:956 / 967
页数:12
相关论文
共 39 条
[1]   An amyloid-forming peptide from the yeast prion Sup35 reveals a dehydrated β-sheet structure for amyloid [J].
Balbirnie, M ;
Grothe, R ;
Eisenberg, DS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (05) :2375-2380
[2]   Synchrotron X-ray studies suggest that the core of the transthyretin amyloid fibril is a continuous beta-sheet helix [J].
Blake, C ;
Serpell, L .
STRUCTURE, 1996, 4 (08) :989-998
[3]   Spectroscopic evidence for amyloid-like interfacial self-assembly of hydrophobin Sc3 [J].
Butko, P ;
Buford, JP ;
Goodwin, JS ;
Stroud, PA ;
McCormick, CL ;
Cannon, GC .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 280 (01) :212-215
[4]   Structural and functional role of the disulfide bridges in the hydrophobin SC3 [J].
de Vocht, ML ;
Reviakine, I ;
Wösten, HAB ;
Brisson, A ;
Wessels, JGH ;
Robillard, GT .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (37) :28428-28432
[5]   Structural characterization of the hydrophobin SC3, as a monomer and after self-assembly at hydrophobic/hydrophilic interfaces [J].
de Vocht, ML ;
Scholtmeijer, K ;
van der Vegte, EW ;
de Vries, OMH ;
Sonveaux, N ;
Wösten, HAB ;
Ruysschaert, JM ;
Hadziioannou, G ;
Wessels, JGH ;
Robillard, GT .
BIOPHYSICAL JOURNAL, 1998, 74 (04) :2059-2068
[6]   Self-assembly of the hydrophobin SC3 proceeds via two structural intermediates [J].
De Vocht, ML ;
Reviakine, I ;
Ulrich, WP ;
Bergsma-Schutter, W ;
Wösten, HAB ;
Vogel, H ;
Brisson, A ;
Wessels, JGH ;
Robillard, GT .
PROTEIN SCIENCE, 2002, 11 (05) :1199-1205
[7]   CHARACTERIZATION OF THE GENOME OF THE BASIDIOMYCETE SCHIZOPHYLLUM-COMMUNE [J].
DONS, JJM ;
DEVRIES, OMH ;
WESSELS, JGH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1979, 563 (01) :100-112
[8]   Amyloid fibrils from muscle myoglobin -: Even an ordinary globular protein can assume a rogue guise if conditions are right. [J].
Fändrich, M ;
Fletcher, MA ;
Dobson, CM .
NATURE, 2001, 410 (6825) :165-166
[9]   A conformation change in the carboxyl terminus of Alzheimer's Aβ(1-40) accompanies the transition from dimer to fibril as revealed by fluorescence quenching analysis [J].
Garzon-Rodriguez, W ;
Vega, A ;
Sepulveda-Becerra, M ;
Milton, S ;
Johnson, DA ;
Yatsimirsky, AK ;
Glabe, CG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (30) :22645-22649
[10]  
GOODWIN JG, UNPUB