Sandbox Reserved 1774

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This Sandbox is Reserved from February 27 through August 31, 2023 for use in the course CH462 Biochemistry II taught by R. Jeremy Johnson at the Butler University, Indianapolis, USA. This reservation includes Sandbox Reserved 1765 through Sandbox Reserved 1795.

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1 Thyroid Stimulating Hormone Receptor (TSHR) Structure and Function

Thyroid Stimulating Hormone Receptor (TSHR) Structure and Function

Introduction

Figure 1: TSHR binds TSH in the HPT signaling axis pathway, which regulates metabolism and growth.

In humans, the hypothalamic-pituitary-thyroid (HPT) signaling axis regulates functions including metabolism, growth, organ development, and neural differentiation ^[1]. In this pathway, the thyroid stimulating hormone receptor (TSHR) activates transcription of thyroid hormones in response to ligand binding by thyroid stimulating hormone (TSH). After a brief introduction to the biological significance of TSHR, this page explores the structure of TSHR and its significance to TSH binding and receptor activation.

Biological Significance of TSHR

The HPT signaling axis involves the brain, thyroid gland, and bloodstream circulation. In the first step of the pathway, thyrotropin releasing hormone (TRH) is secreted by the hypothalamus, which in turn stimulates the anterior pituitary gland to produce TSH ^[1]. TSH binds to TSHR on the surface of thyroid cells and triggers the production of thyroid hormones thyroxine (T3) and triiodothyronine (T4) through G-protein coupled receptor (GPCR) signaling ^[2]. T3 and T4 circulate in the bloodstream and enter cells via thyroid hormone transporters to regulate metabolic functions. Additionally, T3 and T4 act in a negative feedback loop to inhibit further TSH production ^[1].

Dysregulation of TSHR can lead to disease. In Grave's disease, antibody analogs of TSH cause overactivation of TSHR, leading to clinical symptoms of hyperthyroidism ^[2]. In contrast, congenital mutations which inactivate TSHR can lead to hypothyroidism, which results in growth retardation and neurologic impairment if left untreated ^[1].

Structural Overview of TSHR

Describe the domains here.

TSHR Activation

Hinge Motion

Central to the biological function of TSHR is its hinge motion which allows for transition between active and inactive states. Deformation of the hinge region accommodates up-and-down rotation of the extracellular domain as a rigid body about an imaginary 55 degree axis. When the extracellular domain is upright, the receptor actively signals for thyroid hormone production. When the extracellular domain is hinged down, the receptor is inactive and no signaling activation occurs. Notably, transition between the two states occurs spontaneously; favoring of the active or inactive conformation is influenced by hinge interactions and ligand binding ^[3].

At the following link is an animation of TSHR transition between the two states: Image:TSHR MorphBetterAngle.mp4. The following trends can be observed in the video or viewed through an overlay in the molecule viewer:

Slinky-like deformation of the hinge region shifts the N-terminus of the p10 region 5 Angstroms over the course of the movement ^[3].
Stretching of the hinge pulls on the linked helices in the transmembrane domain, shifting helix 7 about 4 Angstroms inward ^[3].

Stabilizing Interactions in the Hinge

To understand stabilizing interactions which accommodate the hinge motion, the hinge region can be subdivided into the hinge helix, which lies at the intersection of the extracellular and transmembrane domains; helix 1, which sticks up and serves as a binding platform for the TSH ligand; the linker region, which connects p10 and helix 1; and the p10 region, a conserved 10-amino acid sequence which undergoes most of the deformation ^[3] ^[4].

Two key disulfide bridges within the hinge region help to maintain its structure and orientation ^[4].

The first disulfide bridge connects the hinge helix with the linker region
The second disulfide bridge connects the hinge helix with the p10 region.

The upright, active conformation of the hinge is stabilized by its respective interactions wit the EC and TM domains ^[3].

A hydrophobic interaction occurs between I486 in the hinge helix and Y279 in loop region 1 of the EC domain.
An ionic interaction occurs between K660 in TM helix 7 and E409 in the p10 region.

This shows the TSHR hinge movement. This shows the TSHR hinge movement. .

Ligand Binding

Ligand-induced Conformation Change

Describe how TSH binds in the upright conformation here.

Ligand Recognition

Describe seatbelt and hinge important to ligand recognition here.

References

↑ ^1.0 ^1.1 ^1.2 ^1.3 Brent GA. Mechanisms of thyroid hormone action. J Clin Invest. 2012;122(9):3035-3043. DOI: 10.1172/JCI60047
↑ ^2.0 ^2.1 Chu YD, Yeh CT. The Molecular Function and Clinical Role of Thyroid Stimulating Hormone Receptor in Cancer Cells. Cells. 2020;9(7):1730. DOI:10.3390/cells9071730
↑ ^3.0 ^3.1 ^3.2 ^3.3 ^3.4 Faust B, Billesbolle CB, Suomivuori CM, Singh I, Zhang K, Hoppe N, Pinto AFM, Diedrich JK, Muftuoglu Y, Szkudlinski MW, Saghatelian A, Dror RO, Cheng Y, Manglik A. Autoantibody mimicry of hormone action at the thyrotropin receptor. Nature. 2022 Aug 8. pii: 10.1038/s41586-022-05159-1. doi:, 10.1038/s41586-022-05159-1. PMID:35940205 doi:http://dx.doi.org/10.1038/s41586-022-05159-1
↑ ^4.0 ^4.1 Duan J, Xu P, Luan X, Ji Y, He X, Song N, Yuan Q, Jin Y, Cheng X, Jiang H, Zheng J, Zhang S, Jiang Y, Xu HE. Hormone- and antibody-mediated activation of the thyrotropin receptor. Nature. 2022 Aug 8. pii: 10.1038/s41586-022-05173-3. doi:, 10.1038/s41586-022-05173-3. PMID:35940204 doi:http://dx.doi.org/10.1038/s41586-022-05173-3

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@@ Line 18: / Line 18: @@
 == TSHR Activation ==
 === Hinge Motion ===
-Central to the biological function of TSHR is its hinge motion which allows for transition between active and inactive states. Deformation of the hinge region accommodates up-and-down rotation of the extracellular domain as a rigid body about an imaginary 55 degree axis. When the extracellular domain is upright, the receptor actively signals for thyroid hormone production. When the extracellular domain is hinged down, the receptor is inactive and no signaling activation occurs. Notably, transition between the two states occurs spontaneously; favoring of the active or inactive conformation is influenced by hinge interactions and ligand binding.
+Central to the biological function of TSHR is its hinge motion which allows for transition between active and inactive states. Deformation of the hinge region accommodates up-and-down rotation of the extracellular domain as a rigid body about an imaginary 55 degree axis. When the extracellular domain is upright, the receptor actively signals for thyroid hormone production. When the extracellular domain is hinged down, the receptor is inactive and no signaling activation occurs. Notably, transition between the two states occurs spontaneously; favoring of the active or inactive conformation is influenced by hinge interactions and ligand binding <ref name="Faust">PMID:35940205</ref>.
 At the following link is an animation of TSHR transition between the two states: [[Image:TSHR_MorphBetterAngle.mp4|Figure 1]]. The following trends can be observed in the video or viewed through an overlay in the molecule viewer:
-#Slinky-like deformation of the hinge region shifts the N-terminus of the p10 region 5 Angstroms over the course of the movement.
+#Slinky-like deformation of the hinge region shifts the N-terminus of the p10 region 5 Angstroms over the course of the movement <ref name="Faust" />.
-#Stretching of the hinge pulls on the linked helices in the transmembrane domain, shifting helix 7 about 4 Angstroms inward.
+#Stretching of the hinge pulls on the linked helices in the transmembrane domain, shifting helix 7 about 4 Angstroms inward <ref name="Faust" />.
 === Stabilizing Interactions in the Hinge ===
-To understand stabilizing interactions which accommodate the hinge motion, the hinge region can be subdivided into the hinge helix, which lies at the intersection of the extracellular and transmembrane domains; helix 1, which sticks up and serves as a binding platform for the TSH ligand; the linker region, which connects p10 and helix 1; and the p10 region, a conserved 10-amino acid sequence which undergoes most of the deformation <ref name="Faust">PMID:35940205</ref> <ref name="Duan">PMID:35940204</ref>.
+To understand stabilizing interactions which accommodate the hinge motion, the hinge region can be subdivided into the hinge helix, which lies at the intersection of the extracellular and transmembrane domains; helix 1, which sticks up and serves as a binding platform for the TSH ligand; the linker region, which connects p10 and helix 1; and the p10 region, a conserved 10-amino acid sequence which undergoes most of the deformation <ref name="Faust" /> <ref name="Duan">PMID:35940204</ref>.
 Two key disulfide bridges within the hinge region help to maintain its structure and orientation <ref name="Duan" />.