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Printable Handouts
Navigable Slide Index
- Introduction
- Chemical protein synthesis
- Emil Fischer- Nobel prize in chemistry (1902)
- HIV-1 protease
- Electronic properties of the catalytic apparatus
- Defining the 'Aspartyl proteases'
- Case study: 'backbone engineering' HIV-1 PR
- Dissecting the energetics of C-cap termination
- The alpha-helix common structural motif
- How does a protein alpha-helix terminate?
- Case study: Ubiquitin (76 aa)
- Conformation vs. solvation effects
- Separting of solvation from conformation effects
- Seven synthetic ubiquitins
- X-ray crystal structure of a protein diastereomer
- Global and local structures are highly conserved
- Stability measurements of [Aaa35] Ubiquitins
- Energetic contributions at helix C' position
- Erythropoietin (Epo)- stimulates hematopoiesis
- Recombinant Epo
- Case study: synthetic erythropoiesis protein
- Synthetic 'glycan mimetic'
- Synthetic scheme
- SEP - analytical data
- SEP - features
- SEP - biological properties
- Glycoprotein synthesis
- Molecular basis of protein function
- The synthetic challenge
- Classical solution synthesis
- Stepwise solid phase synthesis
- Conventional approaches 'stalled out'
- Chemical protein synthesis - re-examined
- Unprotected peptides - a challenge
- Chemical protein synthesis - chemical ligaion
- Principles of chemical ligation
- Thioester- forming ligation
- Total synthesis of D- & L-HIV-1 protease
- Crystal structure of D-HIV-1 protease
- Native chemical ligation (1)
- Thioester-linked ligation product
- Native chemical ligation (2)
- Case study: Crambin (46 aa; 6 Cys)
- Crambin
- Total chemical synthesis of Crambin
- A 'One-Pot' total chemical synthesis of Crambin
- Characterization of synthetic Crambin
- Crambin synthesis - overall yield
- Ligation of unprotected peptides
- Chemical protein synthesis - to date
- Impact of chemical ligation
- CPS current challenges
- Better catalyst for native chemical ligation
- CPS of HIV-1 PR
- Current challenges (1)
- "Middle" segments
- Kinetically-controlled ligation
- Crambin: convergent synthesis
- Crambin synthesis- analytical data
- Targets to which convergent CPS is being applied
- Current challenges (2)
- Solid phase chemical ligation of EETI-II (1)
- Solid phase chemical ligation of EETI-II (2)
- Solid phase chemical ligation of EETI-II (3)
- Folding synthetic proteins
- In vitro folding of synthetic proteins
- AOP-RANTES - folding
- AOP-RANTES- conformational homogeneity
- Crystal structure of AOP-RANTES
- Human secretory PLA4
- CPS - what is the "killer app"?
- 'Single molecule' enzymology
- Entree to a protein world
- Acknowledgements
Topics Covered
- HIV-1 protease
- Electronic properties of the catalytic apparatus
- Defining the 'aspartyl proteases'
- 'Backbone engineering' HIV-1 PR
- The alpha-helix
- Ubiquitin (76 aa)
- Conformation vs. solvation effects
- Global and local structures are highly conserved
- Stability measurements of [Aaa35] ubiquitins
- Energetic contributions at helix C' position
- Erythropoietin (Epo)
- Synthetic erythropoiesis protein
- Synthetic 'glycan mimetic'
- Glycoprotein synthesis
- Molecular basis of protein function
- The synthetic challenge
- Classical solution synthesis
- Stepwise solid-phase synthesis
- Chemical protein synthesis
- Unprotected peptides
- Principles of chemical ligation
- Thioester-forming ligation
- Total synthesis of D- & L-HIV-1 protease
- Crystal structure of D-HIV-1 protease
- Native chemical ligation
- Crambin (46 aa; 6 Cys)
- CPS: current challenges
Talk Citation
Kent, S. (2008, August 14). Chemical protein synthesis: total synthesis of proteins for biological research [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 22, 2024, from https://doi.org/10.69645/UXKO6902.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Stephen Kent has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
Chemical protein synthesis: total synthesis of proteins for biological research
A selection of talks on Biochemistry
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