Sandbox Reserved 1648

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (12:16, 21 January 2022) (edit) (undo)
 
(34 intermediate revisions not shown.)
Line 1: Line 1:
=='''3V6O: Leptin receptor-antibody complex'''==
=='''3V6O: Leptin receptor-antibody complex'''==
-
<StructureSection load='3v6o' size='340' side='right' frame='true' caption='Leptin receptor' scene=''>
+
<StructureSection load='3v6o' size='340' side='right' frame=‘true’ caption='Leptin receptor' scene=''>
-
The '''leptin receptor''', like the hormone that binds to it : [https://en.wikipedia.org/wiki/Leptin '''leptin'''], allows the '''regulation of body weight''' by balancing food intake. It also plays a role in '''reproduction''', '''immunity''' and '''bone metabolism'''.
+
The '''leptin receptor''' also known as LEP-R or OB-R is a protein encoded by the '''LEPR gene'''. It’s a molecule that receives and transmits signals from [https://en.wikipedia.org/wiki/Leptin '''leptin'''], a digestive peptide hormone mostly produced in adipocytes and responsible for the '''feeling of satiety'''.
-
Here, we give an overview of the current structural knowledge of the receptor and its main functions, without omitting its activation, its regulation and its link with some pathologies.
+
Thus, the interaction between the hormone and the leptin receptor allows the '''regulation of body weight''' and the preservation of '''energy homeostasis''' by balancing food intake. It also plays a role in reproduction, immunity and bone metabolism. Leptin receptors belong to the family of [https://en.wikipedia.org/wiki/Type_I_cytokine_receptor '''class 1 cytokine receptors'''].
Line 11: Line 11:
== '''Structure''' ==
== '''Structure''' ==
-
Leptin receptors belong to the family of [https://en.wikipedia.org/wiki/Type_I_cytokine_receptor class 1 cytokine receptors].
+
The leptin receptor protein exists in different forms. Up to now, six ObR isoforms are known named ObRa to ObRf. They are produced by alternative splicing or ectodomain shedding <ref name="refl"> doi: 10.3389/fendo.2017.00030 </ref> .
 +
It consists of an '''extracellular chain''' of 816 amino acids, a '''transmembrane domain''' of 23 amino acids and a '''cytoplasmic domain''' <ref name="ref1"> Le récepteur de la leptine appartient à la famille des récepteurs de cytokines : http://www.ipubli.inserm.fr/bitstream/handle/10608/746/1996_3_386.pdf?sequence=1 </ref> <ref name="ref2"> La leptine : une nouvelle hormone hypo-insulinémiante ? : http://ipubli-inserm.inist.fr/bitstream/handle/10608/532/MS_1997_10_1200.pdf?sequence=1</ref>.
 +
These proteins exists in a '''long form''' and in a '''short forms''' with a cytoplasmic domain of variable size : 302 amino acids for the long form ObRb and 30-40 amino acids for short forms ObRa, ObRc, ObRd, ObRf. There is also a soluble form ObRe <ref name ="refl"> </ref> .
 +
All isoforms have an identical extracellular domain containing 6 functional domains :
-
The leptin receptor protein is a molecule that exists in different forms : short or long. It consists of an '''extracellular chain''' of 816 amino acids, a '''transmembrane domain''' of 23 amino acids and a '''cytoplasmic domain''' <ref name="ref1"> Le récepteur de la leptine appartient à la famille des récepteurs de cytokines : http://www.ipubli.inserm.fr/bitstream/handle/10608/746/1996_3_386.pdf?sequence=1 </ref> <ref name="ref2"> La leptine : une nouvelle hormone hypo-insulinémiante ? : http://ipubli-inserm.inist.fr/bitstream/handle/10608/532/MS_1997_10_1200.pdf?sequence=1</ref>. This cytoplasmic domain is made up of 34 amino acids for the short form of the leptin receptor and 303 amino acids for the long form <ref name="ref2"/>.
+
- an N-terminal domain ('''NTD''')
-
The extracellular part is itself subdivided into 5 functional domains <ref name="ref3"> Leptin receptor : https://en.wikipedia.org/wiki/Leptin_receptor </ref>:
+
- two CRH domains (a distal membrane homology of the first cytokine receptor '''CHR1''' and a second homology of the cytokine receptor '''CRH2''')
-
- distal membrane homology of the first cytokine receptor ('''CRH1'''),
+
- an immunoglobuline-like domain ('''IGD ''' (<scene name='86/868181/Igd/1'>IGD heavy chain</scene> and <scene name='86/868181/Igd/2'>IGD light chain</scene>)) <ref name="refe"> Sequence and annotations Leptin Receptor-antibody complex : https://www.ncbi.nlm.nih.gov/Structure/icn3d/full.html?&mmdbid=97998&bu=1&showanno=1&source=full-feature </ref> <ref name="ref4"> Leptin : https://www.eurofins-biomnis.com/referentiel/liendoc/precis/LEPTINE.pdf </ref>
-
- immunoglobulin-like domain ('''IGD'''),
+
- two additional membrane-proximal fibronectin type III ('''FN III''' (<scene name='86/868181/Fn_iii/1'>single FN III domain</scene> or <scene name='86/868181/Fn_iii/2'>Fn III domains</scene>)) domains <ref> Structure of the Human Obesity Receptor Leptin-Binding Domain Reveals the Mechanism of Leptin Antagonism by a Monoclonal Antibody : https://doi.org/10.1016/j.str.2012.01.019 </ref> <ref name="refl"> </ref> <ref name="refe"> </ref>.
-
 
+
ObR is heavily glycosylated causing an increase of 30-70 kDa in molecular weight <ref name="refl"> </ref> .
-
- second homology of the cytokine receptor ('''CRH2'''),
+
-
 
+
-
- two membrane proximal fibronectine type-III ('''FNIII''') domains.
+
Line 30: Line 30:
Leptin receptors are found in different regions depending on the short or long form of the protein.
Leptin receptors are found in different regions depending on the short or long form of the protein.
-
The long form (Ob-Rl) is mainly present in the [https://en.wikipedia.org/wiki/Hypothalamus '''hypothalamus'''], notably in the [https://en.wikipedia.org/wiki/Arcuate_nucleus arcuate nucleus], [https://en.wikipedia.org/wiki/Dorsomedial_hypothalamic_nucleus dorsomedial] and [https://en.wikipedia.org/wiki/Ventromedial_nucleus_of_the_hypothalamus ventromedial] nuclei, and in the paraventricular nucleus ([https://en.wikipedia.org/wiki/Paraventricular_nucleus_of_hypothalamus PVN]) <ref name="ref4"> Leptin : https://www.eurofins-biomnis.com/referentiel/liendoc/precis/LEPTINE.pdf </ref> <ref name="ref5"> La leptine : votre cerveau, l'appétit et l'obésité : https://www.societe-neuroendocrinologie.fr/Breves/03-La-leptine-votre-cerveau-l-appetit-et-l-obesite </ref> <ref name="ref6"> La leptine : une clé pour la reproduction : http://www.ipubli.inserm.fr/bitstream/handle/10608/1310/1999_2_191.pdf?sequence=2 </ref>. It is also found in lesser amounts in the [https://en.wikipedia.org/wiki/Pancreatic_islets '''islets of Langerhans'''] in mouses, as well as in the '''liver''', '''spleen''', heart''', [https://en.wikipedia.org/wiki/White_adipose_tissue '''white fat'''], [https://en.wikipedia.org/wiki/Lymph_node '''lymph node'''], [https://en.wikipedia.org/wiki/Jejunum '''jejunum'''] and [https://en.wikipedia.org/wiki/Hematopoietic_stem_cell '''hematopoietic stem cells''']<ref name="ref2"/> <ref name="ref7"> Leptine et diabète : http://www.exobiologie.info/diabete/24%20leptine.pdf </ref>.
+
The '''long form''' (Ob-Rb) is mainly present in the [https://en.wikipedia.org/wiki/Hypothalamus '''hypothalamus'''], notably in the [https://en.wikipedia.org/wiki/Arcuate_nucleus arcuate nucleus], [https://en.wikipedia.org/wiki/Dorsomedial_hypothalamic_nucleus dorsomedial] and [https://en.wikipedia.org/wiki/Ventromedial_nucleus_of_the_hypothalamus ventromedial] nuclei, and in the paraventricular nucleus ([https://en.wikipedia.org/wiki/Paraventricular_nucleus_of_hypothalamus PVN]) <ref name="ref4"> </ref> <ref name="ref5"> La leptine : votre cerveau, l'appétit et l'obésité : https://www.societe-neuroendocrinologie.fr/Breves/03-La-leptine-votre-cerveau-l-appetit-et-l-obesite </ref> <ref name="ref6"> La leptine : une clé pour la reproduction : http://www.ipubli.inserm.fr/bitstream/handle/10608/1310/1999_2_191.pdf?sequence=2 </ref>. It is also found in lesser amounts in the [https://en.wikipedia.org/wiki/Pancreatic_islets '''islets of Langerhans'''] in mice, as well as in the '''liver''', '''spleen''', '''heart''', [https://en.wikipedia.org/wiki/White_adipose_tissue '''white fat'''], [https://en.wikipedia.org/wiki/Lymph_node '''lymph node'''], [https://en.wikipedia.org/wiki/Jejunum '''jejunum'''] and [https://en.wikipedia.org/wiki/Hematopoietic_stem_cell '''hematopoietic stem cells''']<ref name="ref2"/> <ref name="ref7"> Hormonal Regulation of Fuel Metabolism : https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/leptin-receptor </ref>.
 +
 
 +
The '''short-form''' (Ob-Ra) is located primarily in the '''lungs''', '''kidneys''' and '''islets of Langerhans''' <ref name="ref4"/>. It is also present in smaller quantities in the brain at the '''hypothalamus'''.<ref name="ref5"/> Ob-Ra is the only form of the protein found in '''ovaries'''. Short form facilitates the passage of leptin across the blood cerebrospinal fluid barrier.
-
Short-form leptin receptors are located primarily in the '''lungs''', '''kidneys''' and '''islets of Langerhans''' <ref name="ref4"/>. In '''ovaries''', only this short form of the protein can be found. The short form Ob-Ra is also present in smaller quantities in the brain at the '''hypothalamus''' <ref name="ref5"/>.
+
Leptin receptors play a role in the regulation of body weight and blunt the drive for food intake, so they are found in '''adipocytes''', '''muscles''', '''hypothalamus'''. Leptin receptors intervene in '''gonads''' to support fertility especially in '''Leydig cells''' in mice, in '''bone marrow''' to promote hematopoiesis and actions in capillary '''endothelium''' to increase angiogenesis <ref name="ref7"> </ref>.
Line 52: Line 54:
== '''Activation''' ==
== '''Activation''' ==
-
The activation of the leptin receptor <ref name="ref3"/> is done through the '''CRH2, IGD and FN III''' domains <ref> The Leptin Receptor Complex: Heavier Than Expected? : https://www.frontiersin.org/articles/10.3389/fendo.2017.00030/full </ref>.
+
The activation of the leptin receptor is done through the '''CRH2, IGD and FN III''' domains <ref> The Leptin Receptor Complex: Heavier Than Expected? : https://www.frontiersin.org/articles/10.3389/fendo.2017.00030/full </ref>.
-
The '''CRH2''' domain is the main leptin binding site on the receptor. This domain is required for the activation of the receptor. It is composed of a region of four consecutive hydrophobic residues. In particular, <scene name='86/868181/Leu_13/1'>Leu13</scene> and '''Leu86''' of leptin interact with '''<scene name='86/868181/Leu_504/1'>Leu504</scene>''' (pink in viewer) in CRH2 forming a bond via hydrophobic interactions<ref>Mapping of the interface between leptin and the leptin receptor CRH2 domain : https://jcs.biologists.org/content/118/11/2519 </ref>. In contrast, the receptor functionality is hardly affected when the CRH1 domain is deleted.
+
The '''CRH2''' domain is the main leptin binding site on the receptor. This domain is required for the activation of the receptor. It is composed of a region of four consecutive hydrophobic residues. In particular, <scene name='86/868181/Leu_13/1'>Leu13</scene> and <scene name='86/868181/Leu_86/1'>Leu86</scene> of leptin interact with '''<scene name='86/868181/Leu_504/2'>Leu504</scene>''' in CRH2 forming a bond via hydrophobic interactions<ref>Mapping of the interface between leptin and the leptin receptor CRH2 domain : https://jcs.biologists.org/content/118/11/2519 </ref>. In contrast, the receptor functionality is hardly affected when the CRH1 domain is deleted.
-
The '''IGD''' domain has no affinity for leptin but is nevertheless '''required''' for receptor activation. In the absence of this domain, the result is a receptor with a wild-type affinity for leptin. However, the receptor is completely devoid of biological activity.
+
The '''IGD''' (<scene name='86/868181/Igd/1'>IGD heavy chain</scene> and <scene name='86/868181/Igd/2'>IGD light chain</scene>) domain has no affinity for leptin but is nevertheless '''required''' for receptor activation. In the absence of this domain, the result is a receptor with a wild-type affinity for leptin. However, the receptor is completely devoid of biological activity <ref name="refe"> </ref> .
-
In the '''FN III''' domains, there are two conserved '''cysteines''' ('''Cys-672 and Cys-751''' <ref>Leptin receptor activation depends on critical cysteine residues in its fibronectin type III subdomains : https://www.jbc.org/article/S0021-9258(20)61429-6/fulltext </ref>) that are crucial for the activation of the receptor.
+
In the '''<scene name='86/868181/Fn_iii/1'>FN III</scene>''' domains, there are two conserved '''cysteines''' ('''Cys-672 and Cys-751''' <ref>Leptin receptor activation depends on critical cysteine residues in its fibronectin type III subdomains : https://www.jbc.org/article/S0021-9258(20)61429-6/fulltext </ref>) that are crucial for the activation of the receptor <ref name="refe"> </ref>.
-
Moreover, in order to form an '''activated 2:4 leptin:ObR complex''', the leptin clusters '''two pre-formed ObR dimers'''.
+
Moreover, in order to form an '''<scene name='86/868181/Activated_leptin_obr_complex/1'>activated 2:4 leptin:ObR complex</scene>'''., the leptin clusters '''two pre-formed ObR dimers'''.
== '''Signaling pathways''' ==
== '''Signaling pathways''' ==

Current revision

3V6O: Leptin receptor-antibody complex

Leptin receptor

Drag the structure with the mouse to rotate

References

  1. 1.0 1.1 1.2 1.3 Wauman J, Zabeau L, Tavernier J. The Leptin Receptor Complex: Heavier Than Expected? Front Endocrinol (Lausanne). 2017 Feb 21;8:30. doi: 10.3389/fendo.2017.00030., eCollection 2017. PMID:28270795 doi:http://dx.doi.org/10.3389/fendo.2017.00030
  2. Le récepteur de la leptine appartient à la famille des récepteurs de cytokines : http://www.ipubli.inserm.fr/bitstream/handle/10608/746/1996_3_386.pdf?sequence=1
  3. 3.0 3.1 La leptine : une nouvelle hormone hypo-insulinémiante ? : http://ipubli-inserm.inist.fr/bitstream/handle/10608/532/MS_1997_10_1200.pdf?sequence=1
  4. 4.0 4.1 4.2 4.3 Sequence and annotations Leptin Receptor-antibody complex : https://www.ncbi.nlm.nih.gov/Structure/icn3d/full.html?&mmdbid=97998&bu=1&showanno=1&source=full-feature
  5. 5.0 5.1 5.2 Leptin : https://www.eurofins-biomnis.com/referentiel/liendoc/precis/LEPTINE.pdf
  6. Structure of the Human Obesity Receptor Leptin-Binding Domain Reveals the Mechanism of Leptin Antagonism by a Monoclonal Antibody : https://doi.org/10.1016/j.str.2012.01.019
  7. 7.0 7.1 La leptine : votre cerveau, l'appétit et l'obésité : https://www.societe-neuroendocrinologie.fr/Breves/03-La-leptine-votre-cerveau-l-appetit-et-l-obesite
  8. La leptine : une clé pour la reproduction : http://www.ipubli.inserm.fr/bitstream/handle/10608/1310/1999_2_191.pdf?sequence=2
  9. 9.0 9.1 Hormonal Regulation of Fuel Metabolism : https://www.sciencedirect.com/topics/agricultural-and-biological-sciences/leptin-receptor
  10. Leptin receptor : https://www.britannica.com/science/leptin-receptor
  11. Leptin in pregnancy and development: a contributor to adulthood disease? : https://journals.physiology.org/doi/full/10.1152/ajpendo.00312.2014
  12. The Leptin Receptor Complex: Heavier Than Expected? : https://www.frontiersin.org/articles/10.3389/fendo.2017.00030/full
  13. Mapping of the interface between leptin and the leptin receptor CRH2 domain : https://jcs.biologists.org/content/118/11/2519
  14. Leptin receptor activation depends on critical cysteine residues in its fibronectin type III subdomains : https://www.jbc.org/article/S0021-9258(20)61429-6/fulltext
  15. Role of OB-RGRP : https://www.institutcochin.fr/linstitut/evenements/ob-rgrp-regulateur-negatif-du-recepteur-de-la
  16. Le récepteur à la leptine et son role dans le développement de l'obésité : https://www.futura-sciences.com/sante/dossiers/medecine-recepteurs-membranaires-point-mire-medicaments-783/page/4/
  17. Polymorphisme des récepteurs de la leptine et de la leptine et perte de grossesse récurrente : https://fre.bioconus.com/leptin-leptin-receptor-polymorphisms-721959
Personal tools