Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 9 de 9
Filter
Add more filters










Database
Language
Publication year range
1.
Animal ; 7 Suppl 2: 235-43, 2013 Jun.
Article in English | MEDLINE | ID: mdl-23739466

ABSTRACT

Ruminant-derived methane (CH4), a potent greenhouse gas, is a consequence of microbial fermentation in the digestive tract of livestock. Development of mitigation strategies to reduce CH4 emissions from farmed animals is currently the subject of both scientific and environmental interest. Methanogens are the sole producers of ruminant CH4, and therefore CH4 abatement strategies can either target the methanogens themselves or target the other members of the rumen microbial community that produce substrates necessary for methanogenesis. Understanding the relationship that methanogens have with other rumen microbes is crucial when considering CH4 mitigation strategies for ruminant livestock. Genome sequencing of rumen microbes is an important tool to improve our knowledge of the processes that underpin those relationships. Currently, several rumen bacterial and archaeal genome projects are either complete or underway. Genome sequencing is providing information directly applicable to CH4 mitigation strategies based on vaccine and small molecule inhibitor approaches. In addition, genome sequencing is contributing information relevant to other CH4 mitigation strategies. These include the selection and breeding of low CH4-emitting animals through the interpretation of large-scale DNA and RNA sequencing studies and the modification of other microbial groups within the rumen, thereby changing the dynamics of microbial fermentation.


Subject(s)
Air Pollutants/metabolism , Archaea/genetics , Bacteria/genetics , Environmental Restoration and Remediation , Genome, Archaeal , Genome, Bacterial , Livestock/microbiology , Methane/metabolism , Animals , Archaea/classification , Bacteria/classification , Breeding , Fermentation , Livestock/genetics , Rumen/metabolism , Rumen/microbiology , Sequence Analysis, DNA/veterinary
2.
J Mol Endocrinol ; 20(2): 233-44, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9584838

ABSTRACT

We have used fragments of the TSH receptor (TSHR) expressed in E. coli as glutathione S-transferase fusion proteins to produce rabbit polyclonal antibodies and a panel (n=5) of monoclonal antibodies to the extracellular fragment of the TSHR. The binding characteristics of the antibodies to linear, conformational, glycosylated and unglycosylated forms of the receptor in different assay systems have been investigated. The reactivity of these antibodies with the TSHR was assessed by Western blotting with both native and recombinant human TSHR expressed in CHO cells, immunoprecipitation of 35S-labelled full-length TSHR produced in an in vitro transcription/ translation system, immunoprecipitation of 125I-TSH/TSHR complexes, inhibition of 125I-TSH binding to the TSHR and fluorescence activated cell sorter (FACS) analysis of binding to CHO-K1 cells expressing the TSHR on their cell surface. Fab fragments of monoclonal antibodies were isolated, labelled with 125I and used to determine the affinity constants of these antibodies with receptor, bound and free Fab being separated by polyethylene glycol (PEG) precipitation. Rabbit polyclonal and mouse monoclonal antibodies reacted with the TSHR in Western blotting and one monoclonal antibody (3C7) was able to inhibit 125I-TSH binding to native human TSHR (74% inhibition), recombinant human TSHR (84% inhibition) and porcine TSHR (65% inhibition). Affinity constant values for TSHR monoclonal antibody Fab fragments calculated using Scatchard analysis were about 10(7) M(-1). Four out of five monoclonal antibodies reacted in FACS analysis with TSHR expressed on the surface of CHO-K1 cells. The FACS unreactive monoclonal (3C7) bound well to detergent solubilised TSH receptors and this emphasised the importance of using a combination of FACS analysis and radioactively-labelled probes in analysis of the TSH receptor. The monoclonal antibodies produced in this study were found to be of relatively low affinity but proved useful for detection of the receptor by Western blotting and by FACS analysis.


Subject(s)
Antibodies, Monoclonal/immunology , Receptors, Thyrotropin/immunology , Animals , Binding Sites, Antibody , Blotting, Western , CHO Cells , Cell Separation , Cricetinae , Female , Flow Cytometry , Humans , Immunoglobulin Fab Fragments/immunology , Rabbits , Receptors, Thyrotropin/metabolism , Recombinant Proteins/immunology , Recombinant Proteins/metabolism , Thyrotropin/metabolism
3.
J Clin Endocrinol Metab ; 79(5): 1517-21, 1994 Nov.
Article in English | MEDLINE | ID: mdl-7962352

ABSTRACT

Autoantibodies to steroid 21-hydroxylase (21-OH) are characteristic of adult onset Addison's disease and we have investigated the effects of these autoantibodies on recombinant human 21-OH enzyme activity. Antibody preparations from 11/11 Addison sera inhibited the ability of 21-OH to convert progesterone to deoxycorticosterone with 8 IgGs showing almost complete inhibition, 2 partial inhibition and 1 weak inhibition. Control IgGs from patients with autoimmune thyroid disease and normal blood donors had little or no effect on 21-OH activity. Our results suggest that 21-OH autoantibodies have the potential to contribute to adrenal failure in Addison's disease by inhibiting the 21-OH enzyme.


Subject(s)
Addison Disease/etiology , Adrenal Insufficiency/immunology , Autoantibodies/physiology , Autoimmune Diseases/etiology , Steroid 21-Hydroxylase/immunology , Steroid 21-Hydroxylase/physiology , Addison Disease/immunology , Adult , Autoantibodies/analysis , Autoantibodies/immunology , Autoimmune Diseases/immunology , Humans , Immunoglobulin G/analysis
4.
J Clin Endocrinol Metab ; 79(2): 372-6, 1994 Aug.
Article in English | MEDLINE | ID: mdl-8045950

ABSTRACT

Human 21-hydroxylase (21-OH) genes containing various mutations, truncations, and deletions were expressed in yeast, and autoantibody binding was studied by Western blotting using patient sera and rabbit antibodies to 21-OH. 21-OH autoantibodies in 13 Addisonian sera showed a marked reduction in their ability to recognize 21-OH mutated at Pro453-->Ser (mean +/- SD, 31 +/- 9% of binding to wild type), whereas the effect on rabbit antibody binding was small (88 +/- 11% of binding to wild type; n = 7). Mutation at Arg339-->His had a less pronounced effect on autoantibody binding (85 +/- 11% of binding to wild type; n = 13) and caused a small enhancement of rabbit antibody binding (124 +/- 16% of binding to wild type; n = 7). These studies indicate that Pro453 has a key role in forming an autoantigenic epitope on 21-OH. It is important to note, however, that the Pro453 mutation caused only partial loss of autoantibody binding, i.e. all Addisonian sera studied still reacted with the mutated protein. This may indicate that each serum sample contains at least two different populations of 21-OH autoantibodies, only one of which recognizes a site dependent on Pro453. A series of more extensive modifications of the 21-OH sequence, including truncations (amino acids 460-494, 448-494, and 418-494) and deletions (amino acids 165-379, 142-240, and 142-280) indicated that most of the sequence of amino acids from 241-494 is important for autoantibody binding. The involvement of such an extensive region of the molecule suggests that the binding sites are generated by three-dimensional folding, with Pro453 having a critical role in forming at least one major autoantigenic epitope.


Subject(s)
Adrenal Glands/immunology , Autoantibodies/metabolism , Mutation , Steroid 21-Hydroxylase/genetics , Steroid 21-Hydroxylase/immunology , Autoantigens/chemistry , Autoantigens/immunology , Base Sequence , Blotting, Western , Gene Deletion , Gene Expression , Humans , Molecular Sequence Data , Mutagenesis, Site-Directed , Restriction Mapping , Saccharomyces cerevisiae/genetics , Steroid 21-Hydroxylase/chemistry , Structure-Activity Relationship
6.
FEBS Lett ; 332(1-2): 123-6, 1993 Oct 11.
Article in English | MEDLINE | ID: mdl-8405426

ABSTRACT

Human steroid 21-hydroxylase (21-OH) expressed in an in vitro translation system was found to react specifically with adrenal autoantibodies from patients with Addison's disease. The epitopes on 21-OH which reacted with autoantibodies were studied by incorporating a series of terminal and internal deletions into the 21-OH gene and analysing the expressed proteins by Western blotting. N-Terminal deletions up to amino acid 280 had no effect on autoantibody binding whereas a series of C-terminal deletions and truncations (amino acids 281-494) showed marked effects. Our results indicate that a central segment (281-379) and a C-terminal segment (380-494) of 21-OH interact to form at least one major autoantibody binding site.


Subject(s)
Addison Disease/immunology , Autoantibodies/immunology , Binding Sites, Antibody , Steroid 21-Hydroxylase/immunology , Adult , Base Sequence , Humans , Molecular Sequence Data , Oligodeoxyribonucleotides , Restriction Mapping , Sequence Deletion , Steroid 21-Hydroxylase/genetics
7.
J Mol Endocrinol ; 10(3): 325-36, 1993 Jun.
Article in English | MEDLINE | ID: mdl-8373516

ABSTRACT

Saccharomyces cerevisiae and the methylotrophic yeast Hansenula polymorpha have been used to express both full-length and a large hydrophilic domain of human thyroid peroxidase (TPO). Expression of TPO in S. cerevisiae, using the natural signal sequence or the yeast alpha-mating factor (MF alpha) signal sequence, resulted in undetectable or very low levels of recombinant TPO production. However, TPO was expressed when the natural TPO leader sequence was replaced by the yeast STE2 signal sequence. This recombinant TPO reacted with both rabbit anti-human TPO polyclonal and mouse anti-human TPO monoclonal antibodies on Western blots. In the case of H. polymorpha, TPO expression was achieved when the natural TPO leader sequence was replaced by the MF alpha leader and the construct placed under the control of the methanol-regulated promoter from the methanol oxidase gene. The recombinant TPO produced in H. polymorpha reacted with both TPO polyclonal and TPO monoclonal antibodies. No TPO was produced when the signal sequence of SUC2 (invertase) or the TPO natural signal sequence was used to direct expression.


Subject(s)
Iodide Peroxidase/genetics , Pichia/genetics , Saccharomyces cerevisiae/genetics , Amino Acid Sequence , Base Sequence , DNA/genetics , Gene Expression , Humans , Molecular Sequence Data , Protein Sorting Signals/genetics , Recombinant Proteins/genetics
8.
FEBS Lett ; 309(1): 51-5, 1992 Aug 31.
Article in English | MEDLINE | ID: mdl-1511745

ABSTRACT

An adrenal-specific protein reacting with autoantibodies in the sera of patients with adult onset Addison's disease has been purified from human adrenal glands. The protein, mol.wt. 55K, has the biochemical characteristics of steroid 21-hydroxylase and reacts on Western blots with rabbit antibodies to recombinant 21-hydroxylase. Absorption of the native human 55K adrenal protein with human adrenal autoantibodies prevented the subsequent reaction of the 55K protein with rabbit antibodies to 21-hydroxylase in Western blot analysis. In addition, human adrenal autoantibodies reacted with recombinant 21-hydroxylase expressed in yeast. These data indicate that the adrenal specific enzyme steroid 21-hydroxylase is a major autoantigen involved in adult onset autoimmune Addison's disease.


Subject(s)
Addison Disease/enzymology , Addison Disease/immunology , Autoantibodies/analysis , Autoantigens/immunology , Steroid 21-Hydroxylase/immunology , Adrenal Glands/immunology , Adult , Blotting, Western , Cloning, Molecular , Electrophoresis, Polyacrylamide Gel , Female , Graves Disease/immunology , Humans , Immunoglobulin G/analysis , Immunoglobulin G/isolation & purification , Microsomes/immunology , Molecular Weight , Placenta/immunology , Pregnancy , Saccharomyces cerevisiae/genetics , Steroid 21-Hydroxylase/genetics , Thyroid Gland/immunology
SELECTION OF CITATIONS
SEARCH DETAIL
...