Structural Elucidation of Specific Noncovalent Association of Folic Acid with Native Cyclodextrins Using an Ion Mobility Mass Spectrometry and Theoretical Approach
PBN-AR
Instytucja
Instytut Medycyny Doświadczalnej i Klinicznej im. Mirosława Mossakowskiego Polskiej Akademii Nauk
Informacje podstawowe
Główny język publikacji
en
Czasopismo
ANALYTICAL CHEMISTRY
ISSN
0003-2700
EISSN
Wydawca
AMER CHEMICAL SOC
DOI
URL
Rok publikacji
2014
Numer zeszytu
9
Strony od-do
4249-4255
Numer tomu
86
Identyfikator DOI
Liczba arkuszy
0,60
Słowa kluczowe
angielski
ELECTROSPRAY-IONIZATION
NDDO APPROXIMATIONS
PROSTATE-CANCER
FOLATE
OPTIMIZATION
COMPLEXES
OLIGONUCLEOTIDE
VITAMIN-B-12
HOMOCYSTEINE
PARAMETERS
Streszczenia
Język
angielski
Treść
The combination of ion mobility mass spectrometry studies and theoretical calculations including docking studies permitted a detailed structural description of noncovalent complexes of folic acid (FA) and native cyclodextrins (alpha-CD, beta-CD, and gamma-CD). The mode of noncovalent association depended on the cavity size of the cyclodextrin. The structure of FA/alpha-CD represented the exclusion complex in which the aminobenzoic moiety and the aromatic pteridine ring of folic acid remain outside the cyclodextrin cavity, while the glutamate residue is anchored in the interior of the alpha-cyclodextrin. A rotaxane-type structure was proposed for the FA/beta-CD complex with the aminobenzoic part of FA being trapped in the central cavity of beta-CD. The glutamate residue and the aromatic pteridine ring interact with the primary and secondary rim hydroxyl residues, respectively, enhancing complex stability. Two possible structures of FA/gamma-CD were suggested, the first one being analogous to the FA/beta-CD complex and the second one being more stable-in which the aromatic pteridine ring penetrates into the CD cavity while the glutamate residue with the aminobenzoic part of FA is exposed to the cone exterior of CD at its wider edge. Further insight into the association behavior of the folic acid toward cyclodextrins evaluated by thermodynamic calculations indicates that the process is highly exothermic. The complex stability increased in the order FA/alpha-CD < FA/beta-CD < FA/gamma-CD. This order is consistent with the previously determined relative gas-phase stability established based on the dissociation efficiency curves of the FA/CD complexes.
Cechy publikacji
ORIGINAL_ARTICLE
Inne
System-identifier
491166
CrossrefMetadata from Crossref logo
Cytowania
Liczba prac cytujących tę pracę
Brak danych
Referencje
Liczba prac cytowanych przez tę pracę
Brak danych