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Recent "affinity" articles

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Expression of 25 human ABC transporters in the yeast Pichia pastoris and characterization of the purified ABCC3 ATPase activity.
Maja Chloupková et al.
Biochemistry 46 (27), 7992-8003 (10 Jul 2007)
 
Cloning, overexpression, and purification of novobiocic acid synthetase from Streptomyces spheroides NCIMB 11891
M Steffensky, S M Li, and L Heide
The Journal of biological chemistry 275 (28), 21754-60 (14 Jul 2000)
 
Purification and initial characterization of the lymphoid-cell protein-tyrosine kinase p56lck from a baculovirus expression system
S E Ramer et al.
Proceedings of the National Academy of Sciences of the United States of America 88 (14), 6254-8 (15 Jul 1991)
 
Synthetic neoglycoconjugates in glycosyltransferase assay and purification
M M Palcic, M Pierce, and O Hindsgaul
Methods in enzymology 247, 215-27 (1994)
 
Cofactor characterization and mechanistic studies of CDP-6-deoxy-delta 3,4-glucoseen reductase: exploration into a novel enzymatic C-O bond cleavage event
V P Miller et al.
Biochemistry 32 (44), 11934-42 (09 Nov 1993)
 
Functional expression of 8-hydroxy-5-deazaflavin-dependent DNA photolyase from Anacystis nidulans in Streptomyces coelicolor
F Mayerl et al.
Journal of bacteriology 172 (10), 6061-5 (Oct 1990)
 
Purification of native bovine carboxylase and expression and purification of recombinant bovine carboxylase
B C Furie et al.
Methods in enzymology 282, 333-46 (1997)
 
Identification of the cellular targets of bioactive small organic molecules using affinity reagents
Chemical Society Reviews 37 (7), 1347 (2008)
 
A high yield affinity purification method for specific RNA-binding proteins: isolation of the iron regulatory factor from human placenta
Nucleic Acids Research 18 (1), 51 (1990)
 
20003 Tabrizchi Proton affinity measurements using ion mobility spectrometry
Proton affinity measurements using ion mobility spectrometry
The Journal of Chemical Thermodynamics 35 (6), 863 (2003)
Abstract Relative proton affinities are usually measured by means of high pressure mass spectrometry. In this work ion mobility spectrometry was used to determine proton affinities. The standard molar enthalpy change ΔH0M for the reaction MH++Nright harpoon over leftM+NH+ was found to be: −(56.3±0.8) kJ·mol−1, when M was ethyl acetate and N ethanol; −(27.8±0.5) kJ·mol−1, when M was acetophenone and N ethyl acetate; −(10.6±0.2) kJ·mol−1, when M was cycloheptanone and N ethyl acetate; −(66.1±1.2) kJ·mol−1, when M was dimethyl methyl phosphonate and N ethyl acetate; and, −(56.7±0.9) kJ·mol−1, when M was dimethyl methyl phosphonate and N cycloheptanone. These values are internally consistent and in good agreement with results obtained with high pressure mass spectrometry. On the basis of proton affinities of cycloheptanone and ethyl acetate, an absolute proton affinity of (902±1.2) kJ·mol−1 has been determined for dimethyl methyl phosphonate. Author Keywords: Proton affinity; Ion mobility spectrometry

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