Class I pathwayPrediction of proteasomal

cleavage and TAP binding

Outline

• MHC class I epitopes– Antigen processing

• Proteasome– Specificity and Polymorphism– Prediction methods

• TAP– Binding motif

• Evolution• Immune escape

Peptide generation in the class I pathway

Proteasomal cleavage

• ~20% of all peptide bonds are cleaved• Average peptide length 6-8 amino acids• Not all peptide bonds are equally likely cleaved

• Cleavage more likely after hydrophobic than after hydrophilic amino acids

Proteasome specificity

• Low polymorphism– Constitutive & Immuno-proteasome

• Evolutionary conserved• Stochastic and low specificity

– Only 70-80% of the cleavage sites are reproduced in repeated experiments

Proteasome evolution (1 unit)

Constitutive

Immuno

Human (Hs) - HumanDrosophila (Dm) - FlyBos Taurus (Bota) - Cow

Oncorhynchus mykiss (Om) - FishArabidopsis thaliana (Didi)- Plant

Trichomonas vaginalis (SP)- Bacteria…

Immuno- and Constitutive proteasome specificity

...LVGPTPVNIIGRNMLTQL..

P1 P1’

Immuno Constitutive

Immuno- and Constitutive proteasome specificity

...LVGPTPVNIIGRNMLTQL..

P1 P1’

Immuno Constitutive

• NetChop– Neural network based method

• PaProc– Partially non-linear method (a neural network without hidden neurons????)

• SMM (stabilized matrix method)• FragPredict

– Based on a statistical analysis of cleavage-determining amino acid motifs present around the scissile bond (i.e. also weight matrix like)

Predicting proteasomal cleavage

NetChop20S-3.0In vitro digest data from the constitutive proteasome

Toes et al., J.exp.med. 2001

NetChop 3.0 Cterm (MHC ligands)

LDFVRFMGVMSSCNNPA LVQEKYLEYRQVPDSDP RTQDENPVVHFFKNIVT TPLIPLTIFVGENTGVP LVPVEPDKVEEATEGEN YMLDLQPETTDLYCYEQ PVESMETTMRSPVFTDN ISEYRHYCYSLYGTTLE AAVDAGMAMAGQSPVLR QPKKVKRRLFETRELTD LGEFYNQMMVKAGLNDD GYGGRASDYKSAHKGLK KTKDIVNGLRSVQTFAD LVGFLLLKYRAREPVTK SVDPKNYPKKKMEKRFV SSSSTPLLYPSLALPAP FLYGALLLAEGFYTTGA

• NetChop-3.0 C-term

– Trained on class I epitopes

– Most epitopes are generated by the immunoproteasome

– Predicts the processing specificity

Predicting proteasomal cleavage

-0.4-0.20

0.20.40.60.81

Performance

FragPredictPAProCI Netchop2.0NetChop3.0

Sens Spec CC

0

0.5

1

Performance

CC PCC Aroc

CC 0.12 0.1 0.41 0.48

PCC 0.13 0.48 0.55

Aroc 0.56 0.82 0.85

FragPredict PAProCI Netchop20S NetChop20S-3.0

NetChop-3.0

NetChop20S--3.0

• Relative poor predictive performance–For MHC prediction CC~0.92 and AUC~0.95

Proteasome specificity

What does TAP do?

TAP affinity prediction

• Transporter Associated with antigen Processing• Binds peptides 9-18 long• Binding determined mostly by N1-3 and C terminal amino acids

TAP binding motif matrix

Peters et el., 2003. JI, 171: 1741.

A low matrix entry corresponds to an amino acid well suited for TAP binding

TAP affinity prediction

Predicting TAP affinity

9 meric peptides >9 meric

Peters et el., 2003. JI, 171: 1741.

ILRGTSFVYV-0.11 + 0.09 - 0.42 - 0.3 = -0.74

Proteasome, TAP and MHC co-evolution

• Antigen processing and presentation is highly ineffective• Only 1 in 200 peptides will bind a given MHC complex• If proteasome and TAP do not effectively produce MHC restricted peptides, antigen processing would be a severe bottleneck for antigen recognition

Co-evolution of Proteasome, TAP and MHC

• CP-P1: Constitutive proteasome specificity at P1 position• TAP-9: TAP motif at P9 position• MHC-9: Average MHC motif at P9

Co-evolution of Proteasome, TAP and MHC

• IP-P1: Immuno proteasome specificity at P1 position• CP-P1: Constitutive proteasome specificity at P1 position• TAP-9: TAP motif at P9 position• MHC-9: Average MHC motif at P9

More evolution

Constitutive proteasome!!!

What is going on at the N terminal?

S T R K F L D G N E M T L . . .

Epitope identification

TAP precursor A2 Epitope FLDGNEMTL

FLDGNEMTL 2.0100 KFLDGNEMTL -2.5300

RKFLDGNEMTL -3.7400 TRKFLDGNEMTL -2.4400

0.0101 0.6483 0.9955 0.9984 0.4299 0.2261 0.0103 0.0265 0.0099 0.0099 0.9590 0.4670 0.9989

Proteasomal cleavage

N terminal trimming

>50% need 2-3 amino acids N terminal trimming

S T R K F L D G N E M T L . . .

0.0101 0.6483 0.9955 0.9984 0.4299 0.2261

Immune escape

• Pathogens evolve under strong selection pressure to avoid CTL recognition

• Generate point mutations or insertions/deletions to disturb– Peptide binding to MHC– CTL recognition

•Only involve the antigenic peptide region

– Antigen processing•Can involve peptide flanking region

Immune escape via antigen processingHIV-1 Nef epitope VPLRPMTY (Milicic et al. JI, 2005, 4618)

IP

IP

CP

Summary

• The most important players (MHC, TAP and proteasome) in the MHC class I pathway have co evolved to a share a common C terminal pathway specificity

• We can predict (up to a degree) proteasomal cleavage • TAP binding motif characterized in a weight matrix

– Binding mostly determined by the N1-3 and C terminal amino acids

• Proteasome produces and TAP transports precursor T cell epitopes of length 8-13 amino acids

• Epitope trimming in the ER by several amino peptidases (ERAP)

• We still do not understand everything– Many more important players are involved in the class I path way