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Tubulin‐tyrosine ligase catalyzes covalent binding of 3‐fluoro‐tyrosine to tubulin: kinetic and [ 19 F]NMR studies
Author(s) -
Monasterio Octavio,
Nova Esteban,
López-Brauet Adamari,
Lagos Rosalba
Publication year - 1995
Publication title -
febs letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.593
H-Index - 257
eISSN - 1873-3468
pISSN - 0014-5793
DOI - 10.1016/0014-5793(95)01099-z
Subject(s) - tyrosine , tubulin , chemistry , covalent bond , stereochemistry , dna ligase , biochemistry , microtubule , enzyme , biology , organic chemistry , microbiology and biotechnology
The use of 3‐fluoro‐tyrosine as an alternative substrate for the enzyme tubulin:tyrosine ligase which catalyzes the incorporation of tyrosine into the α‐tubulin subunit was investigated. The incorporation of tyrosine into tubulin was inhibited competitively by 3‐fluoro‐tyrosine with an apparent K i of ∼ 25 μM. The affinity for this analog was similar to that of tyrosine, confirming that the hydrogen at position 3 of the aromatic ring is not essential for the reaction catalyzed by TTLase. The incorporation of 3‐fluoro‐tyrosine into the C‐terminus of the α‐turbulin subunit was demonstrated through [ 19 F]NMR spectroscopy. The 3‐fluoro‐tyrosine signal at −58.6 ppm (trifluoroacetic acid as external standard), with a bandwidth of 24.7 Hz presented a chemical shift of 0.75 ppm upfield and an enlargement in the bandwidth (30.5 Hz) when incorporated into tubulin. These results strongly suggest that this amino acid is exposed to the solvent in tubulin. Tubulin covalently labeled with 3‐fluoro‐tyrosine was competent to polymerize into microtubules. The use of fluorinated tubulin in [ 19 F]NMR spectroscopy for studying questions concerning protein conformation and interactions will be discussed.