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Topic:Spectroscopy

Spectroscopy is an analytical technique used to measure the interaction between matter and electromagnetic radiation. In equine research, spectroscopy is applied to assess various biological and chemical properties of horses. Techniques such as infrared spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, and mass spectrometry are utilized to analyze tissues, fluids, and other biological samples. These methods provide insights into metabolic processes, nutritional status, and disease states in horses. Spectroscopy aids in the identification and quantification of biomolecules, contributing to the understanding of equine physiology and pathology. This page compiles peer-reviewed research studies and scholarly articles that explore the application, methodology, and findings of spectroscopic techniques in equine science.
Less common “doping” agents and substances encountered during routine screening for drugs.
British journal of sports medicine    October 1, 1976   Volume 10, Issue 3 171-176 doi: 10.1136/bjsm.10.3.171
Haywood PE, Chalmers P.The chromatographic and spectroscopic properties of several unusual substances which have been detected in the "alkaloidal" chloroform extract from racehorse urine and saliva samples are reported. Some of these substances have been identified by combined gas chromatography-mass spectrometry and the source of the substance is stated where this is known. Other substances whose identity is not known have been detected and their mass spectra show characteristic amine fragments. The occurrence of these unidentified substances is more frequent in aged urine samples and it would therefore appear that...
Titration behavior of individual tyrosine residues of myoglobins from sperm whale, horse, and red kangaroo.
The Journal of biological chemistry    September 10, 1976   Volume 251, Issue 17 5187-5194 
Wilbur DJ, Allerhand A.The titration behavior of individual tyrosine residues of myoglobins has been studied by observing the pH dependence of the chemical shifts of Czeta and Cgamma of these residues in natural abundance of 13C Fourier transform NMR spectra (at 15.18 MHz, in 20-mm sample tubes, at 37 degrees) of cyanoferrimyoglobins from sperm whale, horse, and red kangaroo. A comparison of the pH dependence of the spectra of the three proteins yielded specific assignments for the resonance of Tyr-151 (sperm whale) and Tyr-103 (sperm whale and horse). Selective proton decoupling yielded specific assignments for Cze...
A comparison of techniques for the quantitative analysis of hyaluronic acid in equine synovial fluid.
Canadian journal of comparative medicine : Revue canadienne de medecine comparee    April 1, 1976   Volume 40, Issue 2 202-208 
Marsh JA, Hallett FR, Owen RR.A comparison of methods of preparing the hyaluronic acid of equine synovial fluid for quantitative spectrophotographic analysis is presented. A new method is proposed which appears superior to the previous methods.
Inactivation of horse liver alcohol dehydrogenase by modification of cysteine residue 174 with diazonium-1H-tetrazole.
Biochemistry    March 9, 1976   Volume 15, Issue 5 1087-1093 doi: 10.1021/bi00650a021
Sogin DC, Plapp BV.Diazonium-1H-tetrazole was tested as a potential active-site-directed reagent for amino acid residues involved in catalysis by alcohol dehydrogenase. In a novel reaction with a protein, diazonium-1H-tetrazole inactivated the enzyme selectively, and almost stoichiometrically, but reacting with the sulfur of a cysteine residue, Cys-174. As a model compound, the tetrazole adduct of free cysteine was prepared. Elementary and spectral analyses of the adduct were consistent with the structure 5-tetrazoleazo-S-cysteine. The adduct absorbs light with a maximun at 316 nm, and is destroyed by irradiatio...
Inhibition of horse muscle acylphosphatase by pyridoxal 5′-phosphate.
Biochimica et biophysica acta    June 24, 1975   Volume 391, Issue 2 486-493 doi: 10.1016/0005-2744(75)90272-7
Ramponi G, Manao G, Camici G, White GF.It has been shown that horse muscle acylphosphatase is inhibited by pyridoxal 5'-phosphate and that the inhibition is pH dependent, reversible and competitive with respect to substrate binding. Spectral analysis on the EI complex demonstrates the presence of a Schiff base. Reduction of the pyridoxal 5'-phosphate-inhibited enzyme with sodium borohydride, followed by amino acid analysis, produces a diminution of the free lysine peak and the appearance of a new peak corresponding to epsilon-pyridoxyllysine. The results suggest that there is at least one NH2-lysyl residue of horse muscle acylphosp...
Binding of Au(CN)2- and Pt(CN)4-2- to horse liver alcohol dehydrogenase. A 35C1NMR relaxation study.
Biochimica et biophysica acta    January 23, 1975   Volume 377, Issue 1 1-8 doi: 10.1016/0005-2744(75)90279-x
Bull TE, Lindman B, Einarsson R, Zeppezauer M.The binding of Au(CN)2- and Pt(CN)4-2- ions to the coenzyme binding site of horse liver alcohol dehydrogenase (alcohol : NAD+ oxidoreductase EC 1.1.1.1) has been studied by 35C1 nuclear magnetic relaxation. Longitudinal relaxation rates were analyzed in terms of a simple model and binding constants for Au(CN)2-, Pt(CN)4-2- and C1- were estimated. From a comparison between transverse and longitudinal relaxation rates the correlation time and the quadrupole coupling constant of bound chloride ion were obtained. The quadrupole coupling constant estimated from a simple electrostatic model for chlo...
Conformational studies of equilibrium structures in fragments of horse heart cytochrome c.
European journal of biochemistry    January 2, 1975   Volume 50, Issue 2 367-374 doi: 10.1111/j.1432-1033.1975.tb09812.x
Toniolo C, Fontana A, Scoffone E.Ultraviolet absorption and circular dichroism studies have been carried out on horse heart apo-cytochrome c and heme-free peptide fragments obtained by cyanogen bromide cleavage of the native protein. It was noted that the various peptides assume predominantly an unordered conformation in water solution. Increasing ionic strength and addition of 2-chloroethanol increase the right-handed helical content. Guanidinium hydrochloride favors the coil state. It was also demonstrated that two non-interacting helical regions of different stability are present in the apo-protein in 2-chloroethanol.
Photooxidation of horse and sperm-whale myoglobin sensitized by the heme group.
Photochemistry and photobiology    October 1, 1974   Volume 20, Issue 4 357-369 doi: 10.1111/j.1751-1097.1974.tb06588.x
Folin M, Gennari G, Jori G.The irradiation of horse and sperm-whale Fe” or Fez’ myoglobins with visible light showed that axial ligands that render the heme diamagnetic (e.g. 02, CO or CN-) endow the hemoproteins with a marked photosensitivity. In contrast, high-spin myoglobins are unaffected by visible light. These findings appear to be of general validity for all hemo-proteins and are in agreement with the involvment of the triplet state of the heme as the reactive intermediate. In all cases, the overall photoprocess occurs within a very narrow spatial range, leading to specific modification of these photoox...
Cytochrome c: a thermodynamic study of the relationship among oxidation state, ion-binding and structural parameters. Cation binding to horse-heart ferrocytochrome c.
European journal of biochemistry    July 15, 1974   Volume 46, Issue 2 387-391 doi: 10.1111/j.1432-1033.1974.tb03631.x
Margalit R, Schejter A.The specific binding of cations to horse heart ferrocytochrome c has been studied, using the gel filtration method. The cations investigated were: Mg2+, Co2+, cinchonine and proflavine. The stability constants are in the range of 5-8 mM-1, and the number of binding sites per protein molecule are 1 to 2. The temperature dependence of the stability constant for the Mg2+-ferrocytochrome system was measured. The thermodynamic parameters were found to be: dH&s = 4-12 kcal/mol, dG;,, (25 "C) = -5.6 kcal/mol and AS&, = +57 calxmol-lx K-I.
Intrinsic fluorescence of a protein devoid of tyrosine and tryptophan: horse hepatocuprein.
FEBS letters    February 15, 1974   Volume 39, Issue 2 164-166 doi: 10.1016/0014-5793(74)80042-6
Agro AF, Albergoni V, Cassini A.No abstract available
Application of inductively-coupled plasma excitation sources to the determination of trace metals in microliter volumes of biological fluids.
Clinical chemistry    August 1, 1973   Volume 19, Issue 8 807-812 
Kniseley RN, Fassel VA, Butler CC.No abstract available
Proton magnetic resonance study of the histidine residues of sperm whale and horse myoglobins.
Journal of molecular biology    November 14, 1972   Volume 71, Issue 2 513-519 doi: 10.1016/0022-2836(72)90367-1
Cohen JS, Hagenmaier H, Pollard H, Schechter AN.No abstract available
Spectroscopic properties of N-bromosuccinimide-modified horse heart cytochrome c + .
Biochemistry    November 7, 1972   Volume 11, Issue 23 4209-4216 doi: 10.1021/bi00773a003
Myer YP, Pal PK.No abstract available
35 C1 NMR studies of the active site zinc of horse liver alcohol dehydrogenase.
Biochemical and biophysical research communications    December 17, 1971   Volume 45, Issue 6 1444-1450 doi: 10.1016/0006-291x(71)90182-3
Ward RL, Happe JA.No abstract available
Renal electron spin resonance spectra in several species of mammals.
Archives internationales de physiologie et de biochimie    October 1, 1971   Volume 79, Issue 4 801-803 
Maréchal R, Barac G.No abstract available
Relative dye-binding capacity of albumin from several species with HABA, bromocresol green and Spectru AB-2.
Analytical biochemistry    October 1, 1971   Volume 43, Issue 2 575-581 doi: 10.1016/0003-2697(71)90289-2
Pemberton JR, DeJong J.No abstract available
Three dimensional fourier synthesis of horse deoxyhaemoglobin at 2.8 Angstrom units resolution.
Nature    November 7, 1970   Volume 228, Issue 5271 551-552 doi: 10.1038/228551a0
Bolton W, Perutz MF.No abstract available
Optical rotatory dispersion and circular dichroism of horse myoglobin and its derivatives.
Journal of biochemistry    May 1, 1969   Volume 65, Issue 5 759-766 doi: 10.1093/oxfordjournals.jbchem.a129075
Samejima T, Kita M.No abstract available
Measurement of ligand-induced conformational changes in hemoglobin by circular dichroism.
Proceedings of the National Academy of Sciences of the United States of America    May 1, 1969   Volume 63, Issue 1 205-212 doi: 10.1073/pnas.63.1.205
Simon SR, Cantor CR.The UV circular-dichroism spectra of human and horse hemoglobins have been determined at various degrees of partial saturation with oxygen. Spectra of the two native hemoglobins were compared with spectra of the corresponding proteins modified with a reagent known to eliminate the conformational rearrangement normally associated with cooperativity. Such comparison indicates that one region, around 260 mmu, is sensitive chiefly to the state of the hemes; changes in another region, around 285 mmu, may be correlated with the conformational transformation linked to cooperative interactions. All ci...
Comparison of protein structure in the crystal and in solution. V. Solubility of horse methemoglobin and azide binding.
Journal of molecular biology    August 14, 1968   Volume 35, Issue 3 477-481 doi: 10.1016/s0022-2836(68)80007-5
Rupley JA, Gates V.No abstract available
Electron-probe microanalysis of horse dentin.
Journal of electron microscopy    January 1, 1966   Volume 15, Issue 2 86-89 
Takuma S, Katagiri S, Ozasa S.No abstract available
[Study of the spiralization of hemoglobin by optical activity dispersion].
Biofizika    January 1, 1966   Volume 11, Issue 5 773-778 
Vol'kenshteĭn MV, Shemelin AK.No abstract available
Refractive index dispersion in equine hemoglobin solutions.
The Journal of physical chemistry    September 1, 1965   Volume 69, Issue 9 3188-3193 doi: 10.1021/j100893a513
Orttung WH, Warner J.No abstract available
[Anomalous dispersion of the optical activity of dolphin myoglobin and horse hemoglobin].
Biokhimiia (Moscow, Russia)    January 1, 1965   Volume 30, Issue 1 148-152 
Vol'kenshteĭn MV, Shemelin AK.No abstract available
[Electronic Structure of the Prosthetic Groups and Tertiary Structure in Hemoproteins: I. Magnetic and Optical Properties of Divalent Horse Hemoglobin and Myoglobin under Reversible Detergent Action].
Journal of molecular biology    December 1, 1964   Volume 10 475-487 doi: 10.1016/s0022-2836(64)80067-x
GERSONDE K, NETTER H.No abstract available
Horse Heart Cytochrome C: Spectrophotometric Titration and Viscosity Changes in Alkaline Solution.
Biochemistry    November 1, 1964   Volume 3 1648-1650 doi: 10.1021/bi00899a008
RUPLEY JA.No abstract available
A note on the dielectric dispersion of deuterium oxide solutions of horse hemoglobin.
Biochimica et biophysica acta    June 1, 1959   Volume 33, Issue 2 576-578 doi: 10.1016/0006-3002(59)90158-1
TAKASHIMA S, LUMRY R.No abstract available
[Determination of the approximate sperm concentration of horse semen with the aid of a spectrophotometer].
Journal of the American Veterinary Medical Association    April 1, 1959   Volume 134, Issue 7 314-316 
HAAG FM.No abstract available
Reflectance spectra and some respiratory reactions of bovine, equine and human thrombocytes.
The American journal of physiology    February 1, 1957   Volume 188, Issue 2 415-419 doi: 10.1152/ajplegacy.1957.188.2.415
GOUCHER CR, KOCHOLATY W.No abstract available
[Absorption spectrum of horse serum albumin during alkaline denaturation].
Comptes rendus hebdomadaires des seances de l'Academie des sciences    August 2, 1954   Volume 239, Issue 5 456-458 
ROBERT B, JARRIER M.No abstract available
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