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|pagetype =Blood
 
|pagetype =Blood
 
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=Introduction=
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T-cells rely on Major Histocompatability Complexes (MHC) to present antigen fragments for their recognition.  MHC has evolved to form two classes to present antigen: '''MHC I''' presents digestion fragments from antigen in '''cellular cytoplasm''', and '''MHC II''' presents digestion fragments from antigen in the '''tissue fluid'''.  As such, MHC I tends to bind slightly smaller peptides (~9 amino acids) than MHC II (~15 amino acids).
    
=Classes=
 
=Classes=
    
==MHC I==
 
==MHC I==
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[[Image:MHC I.jpg|thumb|200px|right|'''MHC I presentation pathway, courtesy of B. Catchpole, 2008''']]
 
===Structure===
 
===Structure===
 
* MHC class I is expressed on virtually all nucleated cells
 
* MHC class I is expressed on virtually all nucleated cells
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**** This limits the size of epitope seen by the T-cell receptors
 
**** This limits the size of epitope seen by the T-cell receptors
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===Function===
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===Presentation Pathway===
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*Viral proteins are broken down to peptides by the proteasome and transferred to the endoplasmic reticulum via TAP (Transporters associated with Antigen Processing) molecules
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*In the ER< peptides are processed with empty MHC I molecules and exported to the cell surface for presentation
 
* MHC class I molecules bind antigenic peptides derived from within the cell and present these to the T-cell receptors of '''CD8+ T-cells'''
 
* MHC class I molecules bind antigenic peptides derived from within the cell and present these to the T-cell receptors of '''CD8+ T-cells'''
** E.g. virus-encoded antigen
   
* Endogenously produced proteins are produced in the cell cytoplasm
 
* Endogenously produced proteins are produced in the cell cytoplasm
 
** Intracellular pathogens utilise this cellular metabolic machinery for protein synthesis  
 
** Intracellular pathogens utilise this cellular metabolic machinery for protein synthesis  
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