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The fucose-binding lectin from Ralstonia solanacearum. A new type of beta-propeller architecture formed by oligomerization and interacting with fucoside, fucosyllactose, and plant xyloglucan.

Kostlánová, Nikola (författare)
Mitchell, Edward P (författare)
Lortat-Jacob, Hugues (författare)
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Oscarson, Stefan (författare)
Lahmann, Martina, 1963 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för kemi,Department of Chemistry,Department of Organic Chemistry, Arrhenius Laboratory, Stockholm University, S-10691 Stockholm, Sweden
Gilboa-Garber, Nechama (författare)
Chambat, Gérard (författare)
Wimmerová, Michaela (författare)
Imberty, Anne (författare)
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 (creator_code:org_t)
Elsevier BV, 2005
2005
Engelska.
Ingår i: The Journal of biological chemistry. - : Elsevier BV. - 0021-9258 .- 1083-351X. ; 280:30, s. 27839-49
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Plant pathogens, like animal ones, use protein-carbohydrate interactions in their strategy for host recognition, attachment, and invasion. The bacterium Ralstonia solanacearum, which is distributed worldwide and causes lethal wilt in many agricultural crops, was shown to produce a potent L-fucose-binding lectin, R. solanacearum lectin, a small protein of 90 amino acids with a tandem repeat in its amino acid sequence. In the present study, surface plasmon resonance experiments conducted on a series of oligosaccharides show a preference for binding to alphaFuc1-2Gal and alphaFuc1-6Gal epitopes. Titration microcalorimetry demonstrates the presence of two binding sites per monomer and an unusually high affinity of the lectin for alphaFuc1-2Gal-containing oligosaccharides (KD = 2.5 x 10(-7) M for 2-fucosyllactose). R. solanacearum lectin has been crystallized with a methyl derivative of fucose and with the highest affinity ligand, 2-fucosyllactose. X-ray crystal structures, the one with alpha-methyl-fucoside being at ultrahigh resolution, reveal that each monomer consists of two small four-stranded anti-parallel beta-sheets. Trimerization through a 3-fold or pseudo-3-fold axis generates a six-bladed beta-propeller architecture, very similar to that previously described for the fungal lectin of Aleuria aurantia. This is the first report of a beta-propeller formed by oligomerization and not by sequential domains. Each monomer presents two fucose binding sites, resulting in six symmetrically arranged sugar binding sites for the beta-propeller. Crystals were also obtained for a mutated lectin complexed with a fragment of xyloglucan, a fucosylated polysaccharide from the primary cell wall of plants, which may be the biological target of the lectin.

Ämnesord

NATURVETENSKAP  -- Kemi -- Organisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Organic Chemistry (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

Amino Acid Sequence
Arabinose
analogs & derivatives
chemistry
Binding Sites
Calorimetry
Carbohydrate Conformation
Carbohydrate Sequence
Cell Wall
metabolism
Cloning
Molecular
Crystallography
X-Ray
Dimerization
Disaccharides
chemistry
Diterpenes
chemistry
Epitopes
chemistry
Fucose
chemistry
Genetic Vectors
Glucans
chemistry
Hydrogen Bonding
Kinetics
Lectins
chemistry
Ligands
Models
Molecular
Molecular Sequence Data
Mutation
Oligosaccharides
chemistry
Polysaccharides
chemistry
Protein Binding
Protein Conformation
Protein Structure
Secondary
Protein Structure
Tertiary
Ralstonia solanacearum
metabolism
Recombinant Proteins
chemistry
Sensitivity and Specificity
Sequence Homology
Amino Acid
Surface Plasmon Resonance
Temperature
Thermodynamics
Time Factors
Trisaccharides
chemistry
Xylans
chemistry

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