regrades need to be typed and turned in next tuesday after class

24
Regrades need to be typed and turned in next TUESDAY after class

Post on 21-Dec-2015

222 views

Category:

Documents


2 download

TRANSCRIPT

Page 1: Regrades need to be typed and turned in next TUESDAY after class

Regrades need to be typed and turned in next TUESDAY after class

Page 2: Regrades need to be typed and turned in next TUESDAY after class

X-ray structure of a protein-conducting channel

Page 3: Regrades need to be typed and turned in next TUESDAY after class

Secreted Proteins Have a special sequence on them called a

signal sequence, which directs them to Endoplasmic Reticulum

Ribosome brings the half made protein to ER membrane where it must be thread through the membrane

Sec61 is one of these channels that funnels the protein through to the inside of the ER

Page 4: Regrades need to be typed and turned in next TUESDAY after class

QuickTime™ and aTIFF (Uncompressed) decompressor

are needed to see this picture.

BACKGROUND

-how secreted proteins are made-very ordered and controlled

EndoplasmicReticulum

Sec61/SecY

Page 5: Regrades need to be typed and turned in next TUESDAY after class

Study Show importance of Sec61/SecY for

protein translocation into ER Use M.jannaschii to determine by X-ray

crystollography at 3.2 A Determine the process of how

translocation is carried out

Page 6: Regrades need to be typed and turned in next TUESDAY after class

Mutations Made point mutations in genes of the

subunit to strengthen crystal contact

Page 7: Regrades need to be typed and turned in next TUESDAY after class

Hypothesis Proposed a mechanism of the channel

where it opens for polypeptide translocation by displacement of a PLUG

Page 8: Regrades need to be typed and turned in next TUESDAY after class

How is this plug unlocked The plug is removed so translocation

can occur from the Signal Sequence that is on the polypeptide

Page 9: Regrades need to be typed and turned in next TUESDAY after class

Model from Experimental Work

QuickTime™ and aTIFF (Uncompressed) decompressor

are needed to see this picture.

Page 10: Regrades need to be typed and turned in next TUESDAY after class

Immune System

QuickTime™ and aTIFF (Uncompressed) decompressor

are needed to see this picture.

Page 11: Regrades need to be typed and turned in next TUESDAY after class

Immune Cells Need to be able to present bad guys to

cells that can get rid of them Therefore evolution has created a set of

specially designed proteins for this

Page 12: Regrades need to be typed and turned in next TUESDAY after class

MHC class 1 and class 2 MHC1 on all cells. Binds proteins that are

degraded from inside cell and presents them for monitoring

MHC2 present mostly on antigen presenting cells so

OVERALL IDEA, these are great for binding a variety of proteins in order to display on surface

Page 13: Regrades need to be typed and turned in next TUESDAY after class

Antibodies

-important for binding antigen so that it may be neutralized andtaken up by cells that eat (macrophage)

Page 14: Regrades need to be typed and turned in next TUESDAY after class

Made By B cells Two chains: heavy and light Both have variable and constant regions Variable regions will bind to antigen Change in 1 amino acid of the

sequence is enough for the antibody to be specific for another antigen

Page 15: Regrades need to be typed and turned in next TUESDAY after class

How do we get such wide diversity in the body of antibody Have rearrangements of genes Heavy variable chain is encoded by V,

D, J Light chain is encoded by V and J

Page 16: Regrades need to be typed and turned in next TUESDAY after class

OVERALL PIC Rearrangement is going to give us the

ability to produce a lot of different antibody in case we come across a antigen of that type

Page 17: Regrades need to be typed and turned in next TUESDAY after class

Cell Membranes

QuickTime™ and aTIFF (Uncompressed) decompressor

are needed to see this picture.

Page 18: Regrades need to be typed and turned in next TUESDAY after class

What is in a cell membrane

QuickTime™ and aTIFF (Uncompressed) decompressor

are needed to see this picture.

Page 19: Regrades need to be typed and turned in next TUESDAY after class

What processes occur across a cell membrane Pinocytosis- cell drinking Endocytosis-cell taking up specific

molecules via the molecule binding to a specific membrane protein

Then you have passive diffusion, facilitated diffusion, and active transport

Page 20: Regrades need to be typed and turned in next TUESDAY after class

Basic Unit of the bilayer

QuickTime™ and aTIFF (Uncompressed) decompressor

are needed to see this picture.

Links hydrophillic part to hydrophobic

Page 21: Regrades need to be typed and turned in next TUESDAY after class

The phospholipid has double character

-has two parts: Water loving polar head and water hating hydrophobic tail-this is termed an Amphipathic Molecule-when you through in water by itself, it will energetically surround where the heads interact with each other and the tails are hidden from the water and interact with each other- this is called a micelle

Page 22: Regrades need to be typed and turned in next TUESDAY after class

How do proteins fit into all this?

QuickTime™ and aTIFF (Uncompressed) decompressor

are needed to see this picture.

Page 23: Regrades need to be typed and turned in next TUESDAY after class

Membrane Proteins need to be designed in a way that allows them to energetically exist in the membrane while still being able to carry out their functions

Page 24: Regrades need to be typed and turned in next TUESDAY after class

Kyte-Doolittle plot

QuickTime™ and aTIFF (Uncompressed) decompressor

are needed to see this picture.

-tells you if you protein of interest crosses the membrane-number of peaks tells you how many times it crosses