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- Introduction to Protein Folding and Misfolding
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1. Protein folding and misfolding: from theory to therapy
- Prof. Christopher Dobson
- Stability and Kinetics of Protein Folding
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2. Mechanisms of protein folding reactions
- Prof. Thomas Kiefhaber
- Protein Folding Theory
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3. Mapping disordered proteins with single-molecule FRET
- Dr. Hagen Hofmann
- Protein Folding Simulations
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4. Protein folding
- Prof. Eugene Shakhnovich
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5. Simulating protein folding with full atomistic detail
- Prof. Vijay Pande
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6. Molecular dynamics simulations of protein dynamics, unfolding and misfolding
- Prof. Valerie Daggett
- Protein Folding Inside the Cell: Chaperones
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7. Protein folding Inside the cell: macromolecular crowding and protein aggregation
- Prof. Emeritus R. John Ellis
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8. Chaperone mechanisms in cellular protein folding
- Prof. Dr. F. Ulrich Hartl
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9. Quality control of proteins mislocalized to the cytosol
- Dr. Ramanujan Hegde
- Protein Misfolding and Disease
- Protein Design
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11. Designing proteins with life sustaining activities 1
- Prof. Michael Hecht
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12. Designing proteins with life sustaining activities 2
- Prof. Michael Hecht
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13. Folding and design of helical repeat proteins
- Prof. Lynne Regan
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14. Design and engineering of zinc-finger domains
- Prof. Jacqui Matthews
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15. Prediction and design of protein structures and interactions
- Prof. David Baker
- Amyloid Fibrils: Structure, Formation and Nanotechnology
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16. Amyloid fibrils as functional nanomaterials
- Prof. Juliet Gerrard
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17. Functional amyloid fibrils from fungi and viruses
- Prof. Margaret Sunde
- Intrinsically disordered Proteins
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18. Fuzzy protein theory for disordered proteins
- Prof. Monika Fuxreiter
- Intersection of RNA, translation and protein aggregation.
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19. Expanding roles of RNA-binding proteins in neurodegenerative diseases
- Prof. Aaron D. Gitler
- Proteostasis
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20. Adapting proteostasis to ameliorate aggregation-associated amyloid diseases
- Dr. Jeffery W. Kelly
- Archived Lectures *These may not cover the latest advances in the field
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21. Amyloidosis: disease caused by amyloid
- Prof. Mark Pepys
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22. Protein folding and dynamics from single molecule spectroscopy
- Prof. Dr. Benjamin Schuler
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23. Prion diseases
- Prof. Fred Cohen
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25. Titin I27: a protein with a complex folding landscape
- Dr. Jane Clarke
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26. Novel proteins from designed combinatorial libraries
- Prof. Michael Hecht
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28. The sequence determinants of amyloid fibril formation
- Prof. Fabrizio Chiti
Printable Handouts
Navigable Slide Index
- Introduction
- Repeat proteins
- Why undertake protein design
- Repeat protein vs. globular protein
- Tetratricopeptide repeat (TPR)
- Genomic distribution of proteins with tandem TPRs
- Consensus design of a TPR motif
- CTPR1, CTPR2 and CTPR3
- Introducing co-variation, enhancing stability
- Describing TPR stability by a simple model
- Lots of proteins are needed for a model
- Stability as a function of number of tandem TPRs
- Predictions of the Ising model
- Protein stability on a residue-specific basis
- Protein stability - a range of stability
- Other behaviors explained by the Ising model
- What do the long TPRs look like?
- Crystal structure of CTPR8
- Use of crystal structure of CTPR8
- Super-position of TPR domain of OGT and CTPR8
- Functional design: ligand binding
- Functional design: specific contacts
- The nature of ligand-binding sites in proteins
- CTPR - conserved and active residues
- Hypervariability defines the ligand-binding site
- Analogous to antibody hypervariable regions
- Hypervariablity and binding site - general result?
- Hypervariablity and binding site is a general result
- ANK repeats
- Ligand binding to ANK repeats - binding specificitiy
- Functional design
- Electrostatic interactions modulate binding affinity
- Binding is specific
- Split GFP detection of protein-protein intercations
- Split GFP reports on affinity and specificity
- Identifying TPR domains with novel specificities
- Summary
Topics Covered
- Repeat proteins versus globular proteins
- Consensus design, the role of conserved hydrophobic residues
- Co-variation can modulate stability, but is not essential to specify a stable fold
- Structure and stability of the designed CTPR proteins
- The thermodynamic behavior of repeat proteins in terms of a 1D Ising model
- Amide H-exchange to study stability on a residue specific basis
- The structure of long TPRs
- Hypervariability defines the ligand binding site: a general result
- Functional TPR designs
- Useful designer proteins
- The awesome power of screens and selections
Talk Citation
Regan, L. (2015, August 24). Folding and design of helical repeat proteins [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 25, 2024, from https://doi.org/10.69645/POGJ8178.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Lynne Regan has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Biochemistry
Transcript
Please wait while the transcript is being prepared...
0:00
Hello. This is Lynne Regan and I'm going to be talking to you about protein design,
in particular folding and design of helical repeat proteins.
I'm going to be using our work on TPRs,
tetratricopeptide repeats to illustrate various aspects of protein design,
and to show with specific examples from our work what we can learn from this approach.
0:22
First, I need to just introduce you to
repeat proteins and contrast them with globular proteins.
This first slide, we're looking at four different types of repeat protein;
TPR, HEAT, Leucine rich repeat, Ankyrin repeat.
Which you may well have come across because they're widely distributed throughout nature,
and perform a variety of different functions in a variety of cellular pathways.
And what they typically do is to bind and interact with other molecules,
and aid for complex machines,
and complex arrangements of proteins to perform particular functions.
And it's reasonable to speculate that
their elongated structure helps them to perform these functions,
because it exposes a larger surface area than is possible in globular proteins.
If you look at the green-colored repeat units,
which are evident in the TPR, HEAT,
and Ankyrin repeats particularly,
you'll see that the basic unit is about 20 to 40 amino acids long.
And, to create the protein,
there is a direct repeat in tandem of different numbers of those repeats.
Shown on the picture here are three tandem repeats,
the TPR, many more of the HEAT and five for the Ankyrin repeat.
1:36
There are two reasons that we undertake protein design.
One is to better understand the behavior of natural proteins.
If we can recapitulate all the structural and physical properties
of proteins then we really truly understand how they are put together.
This is a kind of a different approach to those in which we take a natural protein,
and so tinker with its structure and properties by making one or two mutations.
This is kind of starting from scratch and building up.
The second reason for undertaking protein design is
to create proteins with novel interesting activities.
And this of course, is a very exciting aspect that we could make
new proteins that will perform new functions and be useful.