Adaptational assistance in clusters of bacterial chemoreceptors

被引:81
作者
Li, MS [1 ]
Hazelbauer, GL [1 ]
机构
[1] Univ Missouri, Dept Biochem, Columbia, MO 65211 USA
关键词
D O I
10.1111/j.1365-2958.2005.04641.x
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
Sensory adaptation of low-abundance chemoreceptors in Escherichia coli requires assistance from high-abundance receptors, because only high-abundance receptors carry the carboxyl-terminal pentapeptide sequence NWETF that enhances adaptational covalent modification. Using membrane vesicles containing both high-abundance receptor Tar and low-abundance receptor Trg, we observed effective assistance in vitro for all three adaptational modifications: methylation, demethylation and deamidation. These results demonstrated that adaptational assistance involves not only the previously documented assistance for methylation but also assistance for the two CheB- catalysed reactions. We determined rates of assisted methylation and demethylation at many ratios of assisting to assisted receptor. Analysis by a model of assistance indicated one Tar dimer could assist seven Trg dimers in methylation or five in demethylation, defining assistance neighbourhoods. These neighbourhoods were larger than a trimer of homodimers, required only receptors and were minimally affected by formation of signalling complexes. Time courses of assisted Trg methylation in membranes with low amounts of Tar showed that assisting receptors did not diffuse beyond initial neighbourhoods for at least two hours. Taken together, these observations indicate that chemoreceptors can form stable neighbourhoods larger than trimers in the absence of other chemotaxis proteins. Such interactions are likely to occur in natural receptor clusters in vivo.
引用
收藏
页码:1617 / 1626
页数:10
相关论文
共 48 条
[31]   Quantitative modeling of sensitivity in bacterial chemotaxis: The role of coupling among different chemoreceptor species [J].
Mello, BA ;
Tu, YH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (14) :8223-8228
[32]  
MILLIGAN DL, 1988, J BIOL CHEM, V263, P6268
[33]   SITE-DIRECTED MUTATIONS ALTERING METHYL-ACCEPTING RESIDUES OF A SENSORY TRANSDUCER PROTEIN [J].
NOWLIN, DM ;
BOLLINGER, J ;
HAZELBAUER, GL .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 1988, 3 (02) :102-112
[34]   Chemotactic adaptation is altered by changes in the carboxy-terminal sequence conserved among the major methyl-accepting chemoreceptors [J].
Okumura, H ;
Nishiyama, SI ;
Sasaki, A ;
Homma, M ;
Kawagishi, I .
JOURNAL OF BACTERIOLOGY, 1998, 180 (07) :1862-1868
[35]  
PARKINSON JS, 1982, J BACTERIOL, V151, P106, DOI 10.1128/JB.151.1.106-113.1982
[36]   An allosteric model for transmembrane signaling in bacterial chemotaxis [J].
Rao, CV ;
Frenklach, M ;
Arkin, AP .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 343 (02) :291-303
[37]   RECEPTOR INTERACTIONS THROUGH PHOSPHORYLATION AND METHYLATION PATHWAYS IN BACTERIAL CHEMOTAXIS [J].
SANDERS, DA ;
KOSHLAND, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (22) :8425-8429
[38]   Molecular model of a lattice of signalling proteins involved in bacterial chemotaxis [J].
Shimizu, TS ;
Le Novère, N ;
Levin, MD ;
Beavil, AJ ;
Sutton, BJ ;
Bray, D .
NATURE CELL BIOLOGY, 2000, 2 (11) :792-796
[39]  
SIMMS SA, 1987, J BIOL CHEM, V262, P29
[40]   Polar clustering of the chemoreceptor complex in Escherichia coli occurs in the absence of complete CheA function [J].
Skidmore, JM ;
Ellefson, DD ;
McNamara, BP ;
Couto, MMP ;
Wolfe, AJ ;
Maddock, JR .
JOURNAL OF BACTERIOLOGY, 2000, 182 (04) :967-973