User:Helena Colvee Martin/Sandbox 1

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This is a default text for your page '''Helena Colvee Martin/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
This is a default text for your page '''Helena Colvee Martin/Sandbox 1'''. Click above on '''edit this page''' to modify. Be careful with the < and > signs.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.
You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.
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<Structure load='4AY9' size='350' frame='true' align='right' caption='Insert caption here' scene='Insert optional scene name here' />
== '''Background''' ==
== '''Background''' ==
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This structure contains three main components with the colors grey, pink and purple. The grey portion is a G-protein coupled receptor which is a seven transmembrane domain receptor. G-protein receptors are cell surface signaling molecules involved in many essential physiological processes in the human body and its activation is essential for the functioning of FSH. The receptor is composed of 695 amino acids and possesses a molecular mass of 76 kDa, with transmembrane helices. On the other hand the extracellular part of the receptor is glycosylated and has leucine-rich repeats.
This structure contains three main components with the colors grey, pink and purple. The grey portion is a G-protein coupled receptor which is a seven transmembrane domain receptor. G-protein receptors are cell surface signaling molecules involved in many essential physiological processes in the human body and its activation is essential for the functioning of FSH. The receptor is composed of 695 amino acids and possesses a molecular mass of 76 kDa, with transmembrane helices. On the other hand the extracellular part of the receptor is glycosylated and has leucine-rich repeats.
This structure also had two different subdomains, the signal specificity subdomain and the hormone-binding subdomain. The transmembrane domain instead contains two cysteine residues that form disulfide bonds in order to stabilize the structure. The purple and pink residues which are found closer together are the hormone itself.
This structure also had two different subdomains, the signal specificity subdomain and the hormone-binding subdomain. The transmembrane domain instead contains two cysteine residues that form disulfide bonds in order to stabilize the structure. The purple and pink residues which are found closer together are the hormone itself.
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The alpha‐subunit peptide sequence and disulfide bond pattern are very similar in all glycoprotein hormones but the beta‐subunit determines the function of the hormone and dictates the binding to its specific receptor. Both subunits are folded into non-globular cystine structures with three loops that extend from the core motifs and consist of disulfide bridges. The alpha-subunit is always composed of 96 amino acids, and FSH has a beta-subunit of 111 amino acids (FSH β), which provides the hormone with its biological activity that will later use for the interaction with the follicle-stimulating hormone receptors. The sugar portion of FSH is bonded with a covalent bond to the amino acid asparagine and is made of N-acetylgalactosamine, mannose, N-acetylglucosamine, and sialic acid. The different proteins presented in human FSH hormones differ in their degree of glycosylation and sialic acid content.
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The alpha‐subunit peptide sequence and disulfide bond pattern are very similar in all glycoprotein hormones but the beta‐subunit determines the function of the hormone and dictates the binding to its specific receptor. Both subunits are folded into non-globular cystine structures with three loops that extend from the core motifs and consist of disulfide bridges. The alpha-subunit is always composed of 96 amino acids, and FSH has a beta-subunit of 111 amino acids (FSH β), which provides the hormone with its biological activity that will later use for the interaction with the follicle-stimulating hormone receptors. The sugar portion of FSH is bonded with a covalent bond to the amino acid asparagine and is made of N-acetylgalactosamine, mannose, N-acetylglucosamine, and sialic acid. The different proteins presented in human FSH hormones differ in their degree of glycosylation and sialic acid content.
== '''Relevance''' ==
== '''Relevance''' ==
Females experience a decrease in hormone levels at the end of their menstrual cycle which can be detected by the cells of the hypothalamus. These cells will then produce more GnRH that will activate the pituitary gland to produce higher levels of FSH and LH. Due to the rise of the follicle-stimulating hormone a follicle will grow in the ovary which will produce other hormones like inhibin or oestradiol. The hypothalamus will also detect the production of these hormones and decrease the amount of GnRH produced so the FSH can be released. As the follicle keeps growing in the ovary more oestrogen will be produced and this will end in the release of an egg from the mature follicle during ovulation.
Females experience a decrease in hormone levels at the end of their menstrual cycle which can be detected by the cells of the hypothalamus. These cells will then produce more GnRH that will activate the pituitary gland to produce higher levels of FSH and LH. Due to the rise of the follicle-stimulating hormone a follicle will grow in the ovary which will produce other hormones like inhibin or oestradiol. The hypothalamus will also detect the production of these hormones and decrease the amount of GnRH produced so the FSH can be released. As the follicle keeps growing in the ovary more oestrogen will be produced and this will end in the release of an egg from the mature follicle during ovulation.

Revision as of 17:00, 29 April 2021

Follicle-Stimulating Hormone and Receptor

FSH

Drag the structure with the mouse to rotate

References

  1. Hanson, R. M., Prilusky, J., Renjian, Z., Nakane, T. and Sussman, J. L. (2013), JSmol and the Next-Generation Web-Based Representation of 3D Molecular Structure as Applied to Proteopedia. Isr. J. Chem., 53:207-216. doi:http://dx.doi.org/10.1002/ijch.201300024
  2. Herraez A. Biomolecules in the computer: Jmol to the rescue. Biochem Mol Biol Educ. 2006 Jul;34(4):255-61. doi: 10.1002/bmb.2006.494034042644. PMID:21638687 doi:10.1002/bmb.2006.494034042644

Fan, Q. R., & Hendrickson, W. A. (2005). Structure of human follicle-stimulating hormone in complex with its receptor. Nature, 433(7023), 269–277. https://doi.org/10.1038/nature03206 Pardue, A., Dvoretz, I., Wright, C., Custard, A., Barbara, E. and Langat, D. (2017), Follicle Stimulating Hormone and Reproductive Aging. The FASEB Journal, 31: 935.3-935.3. https://doi.org/10.1096/fasebj.31.1_supplement.935.3 Hoffmann, A. B. (2011). Sex Hormones: Development, Regulation and Disorders. Nova Science Publishers, Inc Bank, R. (n.d.). FSH:4ay9. Retrieved March 28, 2021, from http://www.rcsb.org/3d-view/4AY9/1 Follicle-stimulating hormone (FSH). (n.d.). Retrieved March 29, 2021, from https://www.yourhormones.info/hormones/follicle-stimulating-hormone/

 Pang, S. C. (2005). Use of Follicle-Stimulating Hormone for the Treatment of Female Infertility – Current Concepts. Women’s Health, 87–95. https://doi.org/10.1517/17455057.1.1.087

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Helena Colvee Martin

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