Mechanical properties of actin filament networks depend on preparation, polymerization conditions, and storage of actin monomers

被引:92
作者
Xu, JY
Schwarz, WH
Käs, JA
Stossel, TP
Janmey, PA
Pollard, TD
机构
[1] Johns Hopkins Univ, Sch Med, Dept Biophys & Biophys Chem, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Dept Chem Engn, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Dept Anat & Cell Biol, Baltimore, MD 21205 USA
[4] Harvard Univ, Brigham & Womens Hosp, Sch Med, Div Expt Med, Boston, MA 02115 USA
关键词
D O I
10.1016/S0006-3495(98)77979-2
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
This study investigates possible sources for the variance of more than two orders of magnitude in the published values for the shear moduli of purified actin filaments. Two types of forced oscillatory rheometers used in some of our previous work agree within a factor of three for identical samples. Polymers assembled in EGTA and Mg2+ from fresh, gel-filtered ATP-actin at 1 mg/ml typically have an elastic storage modulus (G') of similar to 1 Pa at a deformation frequency of 0.1-1 Hz. G' is slightly higher when actin is polymerized in KCI with Ca2+ and Mg2+. Gel filtration removes minor contaminants from actin but has little effect on G' for most preparations of actin from acetone powder. Storage of actin monomers without frequent changes of buffer containing fresh ATP and dithiothreitol can result in changes that increase the G' of filaments by more than a factor of 10. Frozen storage can preserve the properties of monomeric actin, but care is necessary to prevent protein denaturation or aggregation due to freezing or thawing.
引用
收藏
页码:2731 / 2740
页数:10
相关论文
共 58 条
[1]   G-ACTIN - PREPARATION BY GEL FILTRATION AND EVIDENCE FOR A DOUBLE STRANDED STRUCTURE [J].
ADELSTEIN, RS ;
GODFREY, JE ;
KIELLEY, WW .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1963, 12 (01) :34-&
[2]   Phalloidin binding and rheological differences among actin isoforms [J].
Allen, PG ;
Shuster, CB ;
Kas, J ;
Chaponnier, C ;
Janmey, PA ;
Herman, IM .
BIOCHEMISTRY, 1996, 35 (45) :14062-14069
[3]   QUANTITATION OF CAP-Z IN CONVENTIONAL ACTIN PREPARATIONS AND METHODS FOR FURTHER PURIFICATION OF ACTIN [J].
CASELLA, JF ;
BARRONCASELLA, EA ;
TORRES, MA .
CELL MOTILITY AND THE CYTOSKELETON, 1995, 30 (02) :164-170
[4]  
DREWES G, 1991, J BIOL CHEM, V266, P5508
[5]   DOMAIN-STRUCTURE IN ACTIN-BINDING PROTEINS - EXPRESSION AND FUNCTIONAL-CHARACTERIZATION OF TRUNCATED SEVERIN [J].
EICHINGER, L ;
NOEGEL, AA ;
SCHLEICHER, M .
JOURNAL OF CELL BIOLOGY, 1991, 112 (04) :665-676
[6]   TIGHTLY-BOUND DIVALENT-CATION OF ACTIN [J].
ESTES, JE ;
SELDEN, LA ;
KINOSIAN, HJ ;
GERSHMAN, LC .
JOURNAL OF MUSCLE RESEARCH AND CELL MOTILITY, 1992, 13 (03) :272-284
[7]   SYNCHRONY OF CELL SPREADING AND CONTRACTION FORCE AS PHAGOCYTES ENGULF LARGE PATHOGENS [J].
EVANS, E ;
LEUNG, A ;
ZHELEV, D .
JOURNAL OF CELL BIOLOGY, 1993, 122 (06) :1295-1300
[8]   FORMATION OF LIQUID-CRYSTALS FROM ACTIN-FILAMENTS [J].
FURUKAWA, R ;
KUNDRA, R ;
FECHHEIMER, M .
BIOCHEMISTRY, 1993, 32 (46) :12346-12352
[9]  
GERSHMAN LC, 1994, ADV EXP MED BIOL, V358, P35
[10]   ELASTICITY AND FLOW PROPERTIES OF ACTIN GELS [J].
HVIDT, S ;
JANMEY, PA .
MAKROMOLEKULARE CHEMIE-MACROMOLECULAR SYMPOSIA, 1990, 39 :209-213