Natural methylamine osmolytes, trimethylamine N-oxide and betaine, increase tau-induced polymerization of microtubules

被引:58
作者
Tseng, HC
Graves, DJ [1 ]
机构
[1] Iowa State Univ, Neurosci Program, Ames, IA 50011 USA
[2] Iowa State Univ, Dept Biochem Biophys & Mol Biol, Ames, IA 50011 USA
关键词
D O I
10.1006/bbrc.1998.9382
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 natural osmolyte trimethylamine N-oxide (TMAO) at 200 mM increases the extent and the rate of formation of polymerized microtubule (MT) complex caused by tau. TMAO at this concentration has no effect on tubulin alone. Urea at 200 mM blocks tubulin assembly caused by tau, but this inhibition can be reversed by an equal amount of TMAO. Besides TMAO, betaine, another natural osmolyte, was found to have the same effects on MT as TMAO. On the contrary, glycerol (a carbohydrate osmolyte) and glycine tan amino acid osmolyte) do not increase tau-induced MT assembly. The mechanism by which TMAO and betaine enhance tau's effectiveness is not known, but physical studies suggest that the secondary structure of tau is not appreciably changed by 200 mM TMAO. This is the first report showing that natural osmolytes, TMAO and betaine, at a near physiological concentration are able to stimulate tau-induced tubulin assembly. (C) 1998 academic Press.
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收藏
页码:726 / 730
页数:5
相关论文
共 17 条
[1]   Forcing thermodynamically unfolded proteins to fold [J].
Baskakov, I ;
Bolen, DW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (09) :4831-4834
[2]   THE ASSEMBLY OF MICROTUBULE PROTEIN INVITRO - THE KINETIC ROLE IN MICROTUBULE ELONGATION OF OLIGOMERIC FRAGMENTS CONTAINING MICROTUBULE-ASSOCIATED PROTEINS [J].
BAYLEY, PM ;
BUTLER, FMM ;
CLARK, DC ;
MANSER, EJ ;
MARTIN, SR .
BIOCHEMICAL JOURNAL, 1985, 227 (02) :439-455
[3]  
BRANDT R, 1993, J BIOL CHEM, V268, P3414
[4]   MARK, a novel family of protein kinases that phosphorylate microtubule-associated proteins and trigger microtubule disruption [J].
Drewes, G ;
Ebneth, A ;
Preuss, U ;
Mandelkow, EM ;
Mandelkow, E .
CELL, 1997, 89 (02) :297-308
[5]  
GASKIN F, 1982, METHOD ENZYMOL, V85, P433
[6]   ABNORMAL PHOSPHORYLATION OF THE MICROTUBULE-ASSOCIATED PROTEIN-TAU (TAU) IN ALZHEIMER CYTOSKELETAL PATHOLOGY [J].
GRUNDKEIQBAL, I ;
IQBAL, K ;
TUNG, YC ;
QUINLAN, M ;
WISNIEWSKI, HM ;
BINDER, LI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (13) :4913-4917
[7]   EXPRESSION, PURIFICATION, CHARACTERIZATION, AND DELETION MUTATIONS OF PHOSPHORYLASE-KINASE GAMMA-SUBUNIT - IDENTIFICATION OF AN INHIBITORY DOMAIN IN THE GAMMA-SUBUNIT [J].
HUANG, CYF ;
YUAN, CY ;
LIVANOVA, NB ;
GRAVES, DJ .
MOLECULAR AND CELLULAR BIOCHEMISTRY, 1993, 128 :7-18
[8]   CONTRIBUTION OF THE SURFACE FREE-ENERGY PERTURBATION TO PROTEIN SOLVENT INTERACTIONS [J].
KITA, Y ;
ARAKAWA, T ;
LIN, TY ;
TIMASHEFF, SN .
BIOCHEMISTRY, 1994, 33 (50) :15178-15189
[9]   TAU AS A MARKER FOR ALZHEIMERS-DISEASE [J].
MANDELKOW, EM ;
MANDELKOW, E .
TRENDS IN BIOCHEMICAL SCIENCES, 1993, 18 (12) :480-483
[10]  
NA GC, 1982, METHOD ENZYMOL, V85, P393