Immunoglobulin G: Difference between revisions
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Azeredo et al. J of Exp Med. 2002. 195: 665. |
Azeredo et al. J of Exp Med. 2002. 195: 665. |
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==Use as diagnostic== |
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The measurement of immunoglobulin G can be a diagnostic tool for certain conditions if indicated by certain symptoms.{{fact|August 2012}} |
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Testing of IgG is not indicated for diagnosis of allergy.<ref name="AAAAIfive">{{Citation |author1 = American Academy of Allergy, Asthma, and Immunology |author1-link = American Academy of Allergy, Asthma, and Immunology |date = |title = Five Things Physicians and Patients Should Question |publisher = [[American Academy of Allergy, Asthma, and Immunology]] |work = Choosing Wisely: an initiative of the [[ABIM Foundation]] |page = |url = http://choosingwisely.org/wp-content/uploads/2012/04/5things_12_factsheet_AAAAI.pdf |accessdate = August 14 2012}}</ref><ref name="pearlspitfalls">{{cite PMID|19119701}}</ref> |
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==See also== |
==See also== |
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Revision as of 19:21, 30 August 2012
Immunoglobulin G (IgG) is an antibody isotype. It is a protein complex composed of four peptide chains — two identical heavy chains and two identical light chains arranged in a Y-shape typical of antibody monomers. Each IgG has two antigen binding sites. Representing approximately 75% of serum immunoglobulins in humans, IgG is the most abundant antibody isotype found in the circulation.[1] IgG molecules are synthesized and secreted by plasma B cells.
Functions
Antibodies are major components of the immune system. IgG is the main antibody isotype found in blood and extracellular fluid allowing it to control infection of body tissues. It binds many kinds of pathogen--including viruses, bacteria, and fungi--and protects the body against them using several immune mechanisms: For example, agglutination and immobilization, complement activation (classical pathway), opsonization for phagocytosis, and neutralization of toxins. It also plays an important role in antibody-dependent cell-mediated cytotoxicity (ADCC) and intracellular antibody-mediated proteolysis, in which it binds to TRIM21 (the receptor with greatest affinity to IgG in humans) in order to direct marked virions to the proteasome in the cytosol.[2] IgG is also associated with Type II and Type III Hypersensitivity.
IgG antibodies are generated following class switching and maturation of the antibody response and thus participate predominantly in the secondary immune response.[3] IgG is secreted as a monomer that is small in size allowing it to easily perfuse tissues. It is the only isotype that can pass through the human placenta, thereby providing protection to the fetus in utero. Along with IgA secreted in the breast milk, residual IgG absorbed through the placenta provides the neonate with humoral immunity before its own immune system develops. Colostrum contains a high percentage of IgG, especially bovine colostrum.
Structure
IgG antibodies are large molecules of about 150 kDa composed of four peptide chains. It contains two identical class γ heavy chains of about 50 kDa and two identical light chains of about 25 kDa, thus a tetrameric quaternary structure. The two heavy chains are linked to each other and to a light chain each by disulfide bonds. The resulting tetramer has two identical halves, which together form the Y-like shape. Each end of the fork contains an identical antigen binding site. The Fc regions of IgGs bear a highly conserved N-glycosylation site. The N-glycans attached to this site are predominantly core-fucosylated diantennary structures of the complex type. In addition, small amounts of these N-glycans also bear bisecting GlcNAc and α-2,6-linked sialic acid residues.[4]
Low-frequency internal motion
Immunoglobulin G has a low-frequency wave number of 28 cm−1 in the Raman spectra.[5] This emission has been assigned to the breathing motion in the beta-barrel of nine beta-strands in its V domain.[6] The dynamic mechanism of the "chelate effect" and "trigger effect" of IgG has been analyzed from the angle of low-frequency resonance among the 12 beta-barrels of an IgG molecule.[7]
Subclasses
There are four IgG subclasses (IgG1, 2, 3, and 4) in humans, named in order of their abundance in serum (IgG1 being the most abundant).
| Name | Percent | Crosses placenta easily | Complement activator | Binds to Fc receptor on phagocytic cells |
| IgG1 | 66% | yes (1.47)† | second-highest | high affinity |
| IgG2 | 23% | no (0.8)† | third-highest | extremely low affinity |
| IgG3 | 7% | yes (1.17)† | highest | high affinity |
| IgG4 | 4% | yes (1.15)† | no | intermediate affinity |
| †: Quota cord/maternity concentrations blood. Based on data from a Japanese study on 228 mothers. [8] | ||||
Note: IgG affinity to Fc receptors on phagocytic cells is specific to individual species from which the antibody comes as well as the class. The structure of the hinge regions gives each of the 4 IgG classes its unique biological profile. Even though there is about 95% similarity between their Fc regions, the structure of the hinge regions is relatively different.
In a model of autoantibody mediated anemia using IgG isotype switch variants of an anti erythrocytes autoantibody, it was found that IgG2a was superior to IgG1 in activating complement. Moreover, it was found that the IgG2a isotype was able to interact very efficiently with FcgammaR. As a result, 20 times higher doses of IgG1 in relationship to IgG2a autoantibodies, were requried to induce autoantibody mediated pathology.
Azeredo et al. J of Exp Med. 2002. 195: 665.
Use as diagnostic
The measurement of immunoglobulin G can be a diagnostic tool for certain conditions if indicated by certain symptoms.[citation needed]
Testing of IgG is not indicated for diagnosis of allergy.[9][10]
See also
External links
- Janeway Immunobiology - The structure of a typical antibody (IgG)
- A booklet with everything you wanted to know about IgG subclasses
References
- ^ Junqueira, Luiz C. (2003). Basic Histology. McGraw-Hill. ISBN 0-8385-0590-2.
{{cite book}}: Unknown parameter|coauthors=ignored (|author=suggested) (help) - ^ Mallery DL, McEwan WA, Bidgood SR, Towers GJ, Johnson CM, James LC (2010). "Antibodies mediate intracellular immunity through tripartite motif-containing 21 (TRIM21)". Proc. Natl. Acad. Sci. U.S.A. 107 (46): 19985–19990. doi:10.1073/pnas.1014074107. PMC 2993423. PMID 21045130.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Meulenbroek, A.J.; Zeijlemaker, W.P. (1996).
- ^ "Analysis of immunoglobulin glycosylation by LC-ESI-MS of glycopeptides and oligosaccharides". Proteomics. 8 (14): 2858–2871. 2008. doi:10.1002/pmic.200700968. PMID 18655055.
{{cite journal}}: Unknown parameter|authors=ignored (help) - ^ Painter PC, Mosher LE, Rhoads C (1982). "Low-frequency modes in the Raman spectra of proteins". Biopolymers. 21 (7): 1469–72. doi:10.1002/bip.360210715. PMID 7115900.
{{cite journal}}: Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link) - ^ Chou KC (1985). "Low-frequency motions in protein molecules. Beta-sheet and beta-barrel". Biophys. J. 48 (2): 289–97. doi:10.1016/S0006-3495(85)83782-6. PMC 1329320. PMID 4052563.
{{cite journal}}: Unknown parameter|month=ignored (help) - ^ Chou KC (1987). "The biological functions of low-frequency vibrations (phonons). VI. A possible dynamic mechanism of allosteric transition in antibody molecules". Biopolymers. 26 (2): 285–95. doi:10.1002/bip.360260209. PMID 3828475.
{{cite journal}}: Unknown parameter|month=ignored (help) - ^ Hashira S, Okitsu-Negishi S, Yoshino K (2000). "Placental transfer of IgG subclasses in a Japanese population". Pediatr Int. 42 (4): 337–42. doi:10.1046/j.1442-200x.2000.01245.x. PMID 10986861.
{{cite journal}}: Unknown parameter|month=ignored (help)CS1 maint: multiple names: authors list (link) - ^ American Academy of Allergy, Asthma, and Immunology, "Five Things Physicians and Patients Should Question" (PDF), Choosing Wisely: an initiative of the ABIM Foundation, American Academy of Allergy, Asthma, and Immunology, retrieved August 14 2012
{{citation}}: Check date values in:|accessdate=(help)CS1 maint: multiple names: authors list (link) - ^ Template:Cite PMID