Download presentation
Presentation is loading. Please wait.
Published byRosemary Randall Modified over 9 years ago
1
Graves’ Disease Case: Previously Normal thyroid signaling requires circuit of signaling: hypothalamus, pituitary, thyroid Signaling between any cells requires signals and receptors 5 types of extracellular signaling What they are and how they work 4 classes of receptors (only showed list) Receptors: What are they (describing all of them) Now: More details on the 4 classes of receptors Hypothesizing what goes wrong in Graves’
2
What’s different in a Grave’s disease patient? (hyperthyroidism=increased thyroid function) Patients have increased T3 and T4 in bloodstream YOUR HYPOTHESES? What might make a thyroid put in overtime?
3
Hypothesis : Thyroid being over-stimulated Hypothesis: Mutation in signaling within cell leading increase in thyroid hormone production Normal stimulation results from TSH/receptor interaction How does the thyroid know to react? How does a receptor provide specificity Normal activation is the result of signal transduction second messenger cascade How does signal transduction work? What could have gone wrong?
4
Testing the hypotheses IF hypothesis is true then what is expected? What data would suggest the hypothesis needs to be revised? Hypothesis : Thyroid being over-stimulated Known: Normal stimulation results from TSH/receptor interaction How does the thyroid ‘know’ to react? How does a receptor provide specificity?
5
Protein structure Amino acid sequence and folding environment determine the conformation of a protein Parts of a protein: amino acids Amino acids: 5 characteristic parts If all proteins made of amino acids and all amino acids have the same parts why do proteins do different things?
6
Side chains hold the ‘information’ Conventions for writing and speaking about proteins: The N and C termini Polarity of proteins
7
Can we predict protein structure? Motifs and Domains How do you change a protein’s shape? Alter the chain Change the environment– what it is floating in or binding with
8
Levels of Protein Structure Adapted from: http://www.bmb.psu.edu/courses/bisci004a/chem/profold.jpg Benjamin Cummings. Ltd. 2001http://www.bmb.psu.edu/courses/bisci004a/chem/profold.jpg Primary Structure Secondary Structure
9
Levels of Protein Structure Tertiary Structure
10
Quaternary structure Protein Kinase C Interacting Protein. http://lectures.molgen.mpg.de/ProteinStructure/Levels/quaternary.gif http://lectures.molgen.mpg.de/ProteinStructure/Levels/quaternary.gif
11
TSH Receptor: What level of structure? TSH Receptor: from “The Thyroid Manager” Ch16 Plasma membrane Extracellular Cytosolic
12
Graves’ hypothesis 1: TSH, TSH-Receptor interaction ‘too strong’ According to this hypothesis and what we now know about protein binding…… T3 and T4 levels should be _?_ in Graves’ vs. normal. TSH levels should be __?__ in Graves’ vs. normal TSH/TSH receptor interactions should show __?___ binding constant vs. normal.
Similar presentations
© 2025 SlidePlayer.com. Inc.
All rights reserved.