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Topic:Recombinant Proteins

Recombinant proteins in horses refer to proteins that are genetically engineered and produced through recombinant DNA technology. This involves inserting the gene encoding the desired protein into a host cell, which then expresses and produces the protein. In equine research, recombinant proteins are utilized for various applications, including the development of vaccines, therapeutic agents, and diagnostic tools. These proteins can mimic natural proteins, allowing researchers to study their functions, interactions, and potential uses in treating or preventing equine diseases. This page compiles peer-reviewed research studies and scholarly articles that explore the production, application, and impact of recombinant proteins in equine health and medicine.
Nonregenerative anaemia associated with administration of recombinant human erythropoietin to a Thoroughbred racehorse.
Equine veterinary journal    July 1, 1997   Volume 29, Issue 4 326-328 doi: 10.1111/j.2042-3306.1997.tb03132.x
Woods PR, Campbell G, Cowell RL.No abstract available
Characterization and mutational studies of equine infectious anemia virus dUTPase.
Biochimica et biophysica acta    May 23, 1997   Volume 1339, Issue 2 181-191 doi: 10.1016/s0167-4838(96)00229-4
Shao H, Robek MD, Threadgill DS, Mankowski LS, Cameron CE, Fuller FJ, Payne SL.The macrophage tropic lentivirus, equine infectious anemia virus (EIAV), encodes a dUTPase in the pol gene that is required for efficient replication in macrophages. Two naturally occurring variants of the enzyme were expressed as recombinant proteins in Escherichia coli; metal chelate affinity chromatography was used to purify histidine-tagged recombinant enzymes to greater than 80% homogeneity in a single chromatographic step. Biochemical and enzymatic analyses of these preparations suggest that this method yields dUTPase that is suitable for detailed mutational analysis. Specific activities...
Molecular cloning and functional expression of equine interleukin-1 receptor antagonist.
Veterinary immunology and immunopathology    May 1, 1997   Volume 56, Issue 3-4 221-231 doi: 10.1016/s0165-2427(96)05769-8
Kato H, Ohashi T, Matsushiro H, Watari T, Goitsuka R, Tsujimoto H, Hasegawa A.Equine interleukin-1 receptor antagonist (IL-1ra) was molecularly cloned to establish a basis for cytokine therapy of acute and chronic inflammatory diseases in the horse. cDNA clones encoding the whole coding sequence of equine IL-1ra were isolated from equine peripheral blood mononuclear cells (PBMC) that had been stimulated with lipopolysaccharide (LPS). The equine IL-1ra cDNA obtained in this study contained an open reading frame encoding 177 amino acid residues. The predicted amino acid sequence of equine IL-1ra shared 75.7, 75.3 and 76.3% similarity with sequences of human, murine and ra...
Expression of horse and donkey LH in COS-7 cells: evidence for low FSH activity in donkey LH compared with horse LH.
The Journal of endocrinology    March 1, 1997   Volume 152, Issue 3 371-377 doi: 10.1677/joe.0.1520371
Chopineau M, Martinat N, Troispoux C, Marichatou H, Combarnous Y, Stewart F, Guillou F.Horse (Equus caballus) luteinizing hormone (eLH) and chorionic gonadotrophin (eCG), which have the same amino acid sequence, are unusual in that, although they express only LH activity in equids, they express dual LH and FSH activities in all other species tested. Donkey (Equus asinus) LH (dkLH) and CG (dkCG), which also share an identical peptide backbone, have been less well characterized and conflicting results concerning their FSH activity in heterologous species have appeared in the literature. In order to assess and compare the intrinsic LH and FSH activities of the horse and donkey LHs ...
Application of equine infectious anemia virus core proteins produced in a baculovirus expression system to serological diagnosis.
Microbiology and immunology    January 1, 1997   Volume 41, Issue 12 975-980 doi: 10.1111/j.1348-0421.1997.tb01957.x
Kong XG, Pang H, Sugiura T, Sentsui H, Onodera T, Matsumoto Y, Akashi H.Equine infectious anemia virus (EIAV) core proteins were obtained from a baculovirus expression system. Recombinant baculoviruses (rBVs) highly expressed the Gag precursor and p26 antigens in an rBV-infected Sf21 cell culture supernatant. Enzyme-linked immunosorbent assay (ELISA) and agar gel immunodiffusion (AGID) were conducted using the expressed proteins to detect antibodies from experimentally infected horses. The expressed antigens showed low background levels, high specificity and sensitivity in ELISA and AGID. The results of the serological tests using the expressed antigens were ident...
Biosynthesis and distribution of leucocyte elastase inhibitor. Production of recombinant inhibitor.
Acta biochimica Polonica    January 1, 1996   Volume 43, Issue 3 497-501 
Kasza A, Korpula-Mastalerz R, Rose-John S, Dubin A.The horse leucocyte elastase inhibitor (HLEI), present in neutrophils, monocytes and bone marrow cells, is apparently a cytoplasmic protein which is not released from cells even in response to stimulation with lipopolysaccharide, phorbol ester, tumour necrosis factor alpha, interleukin-1 or elastin degradation products. Although no expression of the inhibitor was detected in neutrophils, both monocytes and bone marrow cells were efficient in its synthesis. Using a new expression vector pREST5d, recombinant inhibitor was produced in a large quantity in a soluble form, with a yield of 88 mg per ...
Characteristics of equine herpesvirus 1 glycoproteins expressed in insect cells.
Veterinary microbiology    September 1, 1995   Volume 46, Issue 1-3 193-201 doi: 10.1016/0378-1135(95)00083-m
Whalley JM, Love DN, Tewari D, Field HJ.A series of recombinant baculoviruses containing genes for glycoproteins C, D, H and L of equine herpesvirus 1 (EHV-1) have been constructed, and the EHV-1 products characterised by gel electrophoresis and immunoblotting. The EHV-1 glycoproteins expressed in insect cells were similar but not identical in apparent sizes to those expressed in EHV-1 infected mammalian cells. Each of the EHV-1 products was recognised by convalescent equine sera, indicating that they were all targets for an equine immune response. Mice immunised with baculovirus-expressed EHV-1 gD and gC acquired an enhanced abilit...
Development and evaluation of an ELISA using recombinant fusion protein to detect the presence of host antibody to equine arteritis virus.
Journal of virological methods    July 1, 1995   Volume 54, Issue 1 1-13 doi: 10.1016/0166-0934(95)00020-u
Chirnside ED, Francis PM, de Vries AA, Sinclair R, Mumford JA.A recombinant glutathione-S-transferase fusion protein expressing amino acids 55-98 of equine arteritis virus (EAV) GL (rGL 55-98) was tested in an ELISA for its ability to detect serum antibodies to EAV. Host antibodies induced following EAV infection bound the recombinant antigen by ELISA. The ELISA specificity and sensitivity were determined with a panel of equine sera including postinfection and postvaccination samples. A good correlation existed between EAV neutralizing antibody titers and ELISA absorbance values (r = 0.827). The sensitivity and specificity of the ELISA were 99.6 and 90.1...
Kinetics of inhibition of replication of vesicular stomatitis virus in blood mononuclear cells of horses after in vitro and in vivo treatment with recombinant equine interferon-beta 1.
American journal of veterinary research    August 1, 1994   Volume 55, Issue 8 1093-1100 
Marquardt J, Heymer J, Heinz H, Adolf GR, Deegen E.Recombinant equine interferon-beta 1 (reqIFN-beta 1) induces an antiviral state in blood mononuclear cells (BMC) of horses. Maximal protection against replication of vesicular stomatitis virus is achieved 6 hours after treatment with IFN in vitro and in vivo. Duration of the protective effect depends on the dose of IFN in vitro and in vivo. Availability of reqIFN-beta 1 in cultures of BMC for up to 48 hours does not prolong the antiviral state. The protective effect on BMC after treatment with IFN has similar duration in vivo and in vitro. Monitoring of the effect of IFN in vivo is, thus, simp...
Formation of sulphmyoglobin during expression of horse heart myoglobin in Escherichia coli.
FEBS letters    March 7, 1994   Volume 340, Issue 3 281-286 doi: 10.1016/0014-5793(94)80154-1
Lloyd E, Mauk AG.Expression of recombinant horse heart myoglobin in Escherichia coli has been found to result in the production of both native and variable amounts (approximately 16-17% total) of two sulphmyoglobin isomers. The recombinant sulphmyoglobin produced consists primarily of the A and B isomers as identified by 1H NMR spectroscopy with no evidence for production of the C isomer. Conversion of recombinant sulphmyoglobin to the native protein can be achieved by reconstitution with protohaem IX. The possible relationship of this observation to recombinant expression of other heme proteins is discussed.
Kinetics and haematological effects of erythropoietin in horses.
Veterinary research    January 1, 1994   Volume 25, Issue 6 568-573 
Jaussaud P, Audran M, Gareau RL, Souillard A, Chavanet I.A plasma kinetic study of erythropoietin (EPO) was carried out in 4 horses after subcutaneous administration (30 IU/kg bwt) of recombinant human erythropoietin (rhEPO). At standardized intervals for 48 h before injection and for 60 h post-administration, the EPO plasma levels were determined with an immunoradiometric assay based on a sandwich technique. The peak plasma concentration (30-113 mIU/ml) was observed after a delay ranging from 6 to 9 h post-administration and the drug levels reached a physiological value around 60 h following rhEPO injection. Moreover, reference values for plasma EP...
A soluble recombinant fusion protein of the transmembrane envelope protein of equine infectious anaemia virus for ELISA.
Veterinary microbiology    June 1, 1992   Volume 31, Issue 2-3 127-137 doi: 10.1016/0378-1135(92)90071-z
Thomas LM, Huntington PJ, Mead LJ, Wingate DL, Rogerson BA, Lew AM.The use of the bacterial expression vector, pGex, to produce an abundant, soluble fusion protein of gp45 from equine infectious anaemia virus is described. Purification of the recombinant protein was achieved by one step affinity chromatography on immobilized glutathione using competitive elution so no harsh conditions were required. This provides a readily available antigen that is defined, plentiful and cheap. Yields of 3.5 mg of purified soluble protein/litre of bacterial culture were obtained. This antigen was found to be suitable for ELISA. Background reactivity to either the glutathione-...
Increased ovulation rates in mares after immunisation against recombinant bovine inhibin alpha-subunit.
Equine veterinary journal    March 1, 1992   Volume 24, Issue 2 144-146 doi: 10.1111/j.2042-3306.1992.tb02800.x
McKinnon AO, Brown RW, Pashen RL, Greenwood PE, Vasey JR.THE name inhibin was first used around 60 years ago for a water-soluble. non-steroidal, gonadal factor that would regulate follicle-stimulating hormone (FSH) secretion through negative feedback McUullagh 1930. Inhihin is now defined as a glycoprotein hormone, consisting of two dissimilar, disulphide-linked, subunits termed at and 13 1 Burger and Igarashi 1988). Effective methods for blocking inhibin production could provide useful means by which FSH secretion, and therefore ovarian function and fertility, could be improved in the female. Increased ovulation rates have been demonstrated in shee...
Gonadotropin-induced up- and down-regulation of ovarian follicle-stimulating hormone (FSH) receptor gene expression in immature rats: effects of pregnant mare’s serum gonadotropin, human chorionic gonadotropin, and recombinant FSH.
Endocrinology    March 1, 1992   Volume 130, Issue 3 1289-1295 doi: 10.1210/endo.130.3.1537292
LaPolt PS, Tilly JL, Aihara T, Nishimori K, Hsueh AJ.The actions of gonadotropins on ovarian differentiation are associated with dynamic changes in gonadotropin receptor content, presumably due to modulation of receptor gene expression. The present studies used a reverse transcription-polymerase chain reaction to obtain a rat FSH receptor cDNA fragment, followed by synthesis of a labeled cRNA probe to examine the regulation of FSH receptor mRNA levels during follicular maturation, ovulation, and luteinization. Northern blot analysis of ovarian RNA with the FSH receptor probe revealed two predominant hybridization signals of 7.0 and 2.5 kilobases...