ChemInform Abstract: C-Terminal Sequencing of Peptides and Proteins by Successive Degradation with Heptafluorobutyric Anhydride Vapor.

ChemInform ◽  
2010 ◽  
Vol 25 (36) ◽  
pp. no-no
Author(s):  
Y. NABUCHI ◽  
H. YANO ◽  
M. KAMO ◽  
K. TAKAMOTO ◽  
K. SATAKE ◽  
...  
2021 ◽  
Author(s):  
Jianmin Ma ◽  
Junda Huang ◽  
Jiandong Liu ◽  
Jian He ◽  
Mingguang Wu ◽  
...  

1987 ◽  
Vol 70 (1) ◽  
pp. 151-160 ◽  
Author(s):  
Samuel L MacKenzie

Abstract The N-heptafluoroburyryl isobutyl derivatives of proteic amino acids are well resolved by gas chromatography and form the basis of a convenient, rapid assay. The derivatives are prepared by acid-catalyzed esterification at 120°C for 20 min in 3N HCl-isobutanol followed by acylation with heptafluorobutyric anhydride at 150°C for 10 min. The reaction sequence is performed without any transfers or extractions and thus is compatible with microscale analysis. A complete proteic amino acid profile can be completed in less than 20 min by using a packed column or less than 10 min by using a capillary column in combination with an elevated oven temperature program rate. Physiological sample matrixes, which frequently contain a complex mixture of components, and thus require maximum resolution, can be assayed in less than 1 h using a program rate of 4°C/min. A capillary column is recommended for this application. Capillary column chromatography, in combination with a nitrogenspecific detector, is useful for identifying and assaying nonproteic amino acids in physiological sample matrixes. Frequently, a prior cleanup of the sample can be avoided.


1978 ◽  
Vol 7 (5) ◽  
pp. 415-418
Author(s):  
J B Brooks ◽  
D S Kellogg ◽  
G Choudhary ◽  
C C Alley ◽  
J A Liddle

Electron capture gas-liquid chromatography and mass spectrometry have been used to identify some of the basic extractable heptafluorobutyric anhydride reactive compounds found in a defined medium after 20 h of growth by Neisseria gonorrhoeae and N. meningitidis. Acetoin, 2,3-butanediol, pyrroline, and 1,3-diaminopropane were identified by both gas chromatography and mass spectrometry; 2-hydroxy-pyrrolidine and 3-aminomethyl-pyrrolidine were tentatively identified by mass spectrometry. A possible origin of the amines is through enzymatic oxidation of polyamines.


1990 ◽  
Vol 55 (10) ◽  
pp. 2460-2467 ◽  
Author(s):  
Pavel Kubát ◽  
Josef Pola

The continuous-wave CO2 laser induced gas-phase decomposition of trifluoroacetic, pentafluoropropionic and heptafluorobutyric anhydride, sensitized by sulfur hexafluoride was studied in order to determine the course of the reactions in the absence of wall effects. The decompositions of all the compounds are assumed to involve cleavage of parent compound into acyl fluoride F(CF2)nCOF and .(CF2)nCO2. biradical, the latter undergoing decay into CO and F(CF2)n-1COF compounds. The theoretical treatment of the biradical by MNDO calculations as well as trapping with ethene are presented.


1975 ◽  
Vol 47 (3) ◽  
pp. 509-512 ◽  
Author(s):  
Terry A. Gough ◽  
Keith. Sugden ◽  
Kenneth S. Webb

1979 ◽  
Vol 25 (2) ◽  
pp. 218-220 ◽  
Author(s):  
L G Davis ◽  
N L Sass ◽  
B Manna ◽  
M L Nusynowitz

Abstract A sensitivie, reliable gas-chromatographic assay for monoiodotyrosine and diiodotyrosine in human serum is reported. The oxazolidinone-heptafluorobutyric anhydride derivatives allow the quantitation of both compounds in the linear range of 0.2 to 7.6 mg/L of serum. Analytical recovery averaged 88%, and mean accuracy and within-run precision were 98 and 2%, respectively. Concentrations of monoiodotyrosine in serum as low as 20 microgram/L and of diiodotyrosine as low as 100 microgram/L can be detected. Normal serum contains no detectable concentration of either compound, but the method is applicable as a diagnostic tool in the early prediction of thyroid disease. Both compounds were detected in the serum of a hypothyroid subject whose normal thyroid hormone concentrations were being maintained by therapy with desiccated thyroid extract.


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