1 / 30

Structure and gating mechanism of the acetylcholine receptor pore

Structure and gating mechanism of the acetylcholine receptor pore. Acetylcholine receptor. Important in transmitting messages from neuron to neuron Is a excitatory neurotransmitter Acetylcholine is stored in vesicles at the end of a neuron

dobry
Download Presentation

Structure and gating mechanism of the acetylcholine receptor pore

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Structure and gating mechanism of the acetylcholine receptor pore

  2. Acetylcholine receptor • Important in transmitting messages from neuron to neuron • Is a excitatory neurotransmitter • Acetylcholine is stored in vesicles at the end of a neuron • When the right signal comes along, it causes the release of acetylcholine into the synaptic cleft • Here it binds to the acetylcholine receptor and which will allow for further transmission of the signal

  3. Propagation of signal from neuron to neuron via neurotransmitters

  4. Acetylcholine receptor • Classic example of a ligand gated channel • So it is a ion channel that is ligand gated • It ultimately leads to an influx of positive ions

  5. Ach Receptor Structure • 5 transmembrane polypeptides and they are 2 alpha, 1 beta, 1 delta, and 1 gamma • Each subunit is made up of 4 transmembrane alpha helices (helical bundle). They are M1-M4

  6. Picture of subunits and M1-M4

  7. Each helices has features • M2 is mostly amphipathic while M1, M3, and M4 are mostly hydrophobic • M2 has polar side chains for the most part in the middle of the pore and hydrophobic backing up against the back of the pore

  8. Inside the channel • In the middle of the channel there are 5 leucine sidechains and these 5 leucine sidechains come 1 from each M2 helix • There function is to protrude into the channel and block it • This is when the channel is in its closed conformation and inactivated

  9. Picture inside the channel

  10. The activated Ach Receptor • Bulky hydrophobic leucines are removed from channel core • This occurs when Ach binds to the receptor • Binding causes conformational change, twisting of the M2 helices and the leucines twist out of the way

  11. The Activated Ach Receptor continued • The M2 helices now instead of having bulky hydrophobic residues now have polar residues facing inward and ions can go down the channel

  12. Picture of Activated Ach Receptor

  13. Ach Receptor Summary • Bulky hydrophobic leucine side chains of M2 helices close the channel • Upon activation from Ach binding, the leucine side chains twist out of the way and now the polar hydrophilic side chains and now positive ions can rush through.

  14. The Paper about Ach Receptor • Used liquid high helium temperatures • Resolved protein structure at 4A • Proposed a mechanism of how the pore opens and closes in response to presence or absence of Ach

  15. Method • Obtained crystals from Torpedo marmorata membranes • Crystals at first did not yield high amplitudes so they adjusted their procedure using Fourier transforms to enhance signal • Used electron imaging to obtain their structures

  16. Signal Transduction • When cells convert an extracellular signal to an intracellular signal that alter the behavior of the target cell

  17. Signal Transduction

  18. Ionotropic Channel Very fast Metabotropic Second messenger slower Recptors

  19. Receptors • Ion-channel-linked (AchR) ionotropic • G-protein linked metabotropic • Enzyme-linked metabotropic involves the covalent modification of P to serine threonine or tyrosine

  20. G protein receptor • 7 transmembrane helices • Links outside to inside of cell

  21. G protein • Made up of three subunits, alpha, beta, and gamma ( A heterotrimeric protein) • The alpha subunit is referred to as the key player in relaying the signal

  22. Mechanism of G protein

  23. Activated G protein leads to the exchange of GDP (inactive form) to GTP (active form) • Then this activated subunit will then go and activate another protein

  24. Alpha Subunit • GTP will bind at a site on this subunit and activate it Gfrom Transducin

  25. Pic of Beta Subunit Beta Subunit • Built from 7 WD repeats ( motifs that are built from tryptophan(W) and aspartate(D) • Beta Propellar formed by seven subunits made of Beta Sheets

  26. Putting it all together • G does not interact with Gbut the are linked by the Gsubunit • GGinteract • Forms functional signaling unit

  27. GEF GDP GTP GAP

  28. Ras protein • Monomeric • Is active when it has GTP bound • Play a role in cell growth and differentiation • GTP linked to Ras via Mg2+

  29. Ras protein

  30. Ras protein with GTP linked to it via Mg2+

More Related