On Sunday, April 20th 2025, starting 8:30am GMT, there will be maintenance work that will involve the website being unavailable during parts of the day. We apologize for any inconvenience this may cause and appreciate your understanding.
We noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
Printable Handouts
Navigable Slide Index
- Introduction
- Proteins export from the ER
- Model for evolutionary origin of nucleus and ER
- "Hawaiian punch" view of the cell
- Specific protein modifications occurr in the ER
- Advantages of eukaryotic secretion system
- Destination of proteins synthesized in the ER
- Proteins traffic through the Golgi apparatus
- Main themes to be further discussed
- COPII vesicle formation involves a cytosolic coat
- Role of Sec13/31 complex in COPII cage formation
- Flexibility of the COPII cage
- Role of Sec23/24 complex in COPII cage formation
- Cargo proteins contain export signals
- Induction of ER membrane curvature by Sar1-GTP
- Sar1 promotes disassembly of the COPII coat
- Homotypic fusion of COPII vesicles
- ER proteins are retrieved from the Golgi
- Transitional ER (tER) sites
- Cellular distribution of mammalian tER sites
- Mammalian tER sites location relative to Golgi
- The ER-Golgi intermediate compartment (ERGIC)
- Microtubules elimination results in Golgi stacks
- A yeast model for the tER-Golgi relationships
- tER and Golgi are adjacent in Pichia
- How do tER sites proliferate?
- Pichia tER sites form de novo and fuse
- A self-organization model for tER site formation
- Sec16 is a key organizer of tER sites
- Mammalian cells contain Sec16 homologs
- Pychia and tER Golgi dynamics are linked
- Golgi organization in Saccharomyces and Pichia
- Two yeasts have different tER organization
- Golgi structure correlates with tER organization
- The Golgi can be formed de novo from the ER
- Model for de novo Golgi biogenesis
- Stability of Golgi cisternae
- Cisternal maturation vs. stable compartments
- S. cerevisiae is ideal for observing Golgi cisternae
- The Saccharomyces Golgi is very dynamic
- Cisternae clearly mature in Saccharomyces
- Conclusions
Topics Covered
- Evolutionary origin of the ER
- Role of the ER in membrane biogenesis
- Export from the ER in COPII transport vesicles
- Clustering of COPII components at transitional ER sites
- Relationship between ER export and the Golgi apparatus
- Cisternal maturation of Golgi compartments
Talk Citation
Glick, B. (2007, October 1). Membrane transport from the endoplasmic reticulum [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved April 15, 2025, from https://doi.org/10.69645/TDFV7700.Export Citation (RIS)
Publication History
- Published on October 1, 2007
Financial Disclosures
- Dr. Benjamin Glick has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.