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Peptide length determines the outcome of T cell receptor/peptide-MHCI engagement
DOI:
10.1182/blood-2012-06-437202
PMID:
23255554
Authors:
J.
Ekeruche-makinde
(Cardiff University, U.K.)
,
John
Miles
(Cardiff University)
,
H. A.
Van Den Berg
,
A.
Skowera
,
D. K.
Cole
(Cardiff University, U.K.)
,
G.
Dolton
(Cardiff University, U.K.)
,
A. J. A.
Schauenburg
(Cardiff University, U.K.)
,
M. P.
Tan
(Cardiff University, U.K.)
,
J. M.
Pentier
(Cardiff University, U.K.)
,
S.
Llewellyn-lacey
(Cardiff University, U.K.)
,
K. M.
Miles
(Cardiff University, U.K.)
,
A. M.
Bulek
(Cardiff University, U.K.)
,
M.
Clement
(Cardiff University, U.K.)
,
T.
Williams
(Cardiff University, U.K.)
,
A.
Trimby
(Cardiff University, U.K.)
,
M.
Bailey
(University of Bristol, U.K.)
,
Pierre
Rizkallah
(Cardiff University)
,
J.
Rossjohn
(Cardiff University, U.K.)
,
M.
Peakman
(King's College London, U.K.)
,
D. A.
Price
(Cardiff University, U.K.)
Co-authored by industrial partner:
No
Type:
Journal Paper
Journal:
Blood
, VOL 121 (7)
, PAGES 1112-1123
State:
Published (Approved)
Published:
December 2012
Abstract: MHCI-restricted TCRs exhibit an explicit preference for a single MHCI-peptide length. Effective CD8+ T-cell immunity can only be achieved by length-matched Ag-specific T-cell clonotypes.
Journal Keywords: Antigen; Antigens ; CD8-Positive; Clone; Histocompatibility; Humans ; Immunity ; Cellular ; Models ; Molecular ; Oligopeptides ; Peptide; Peptide; Receptors ; Antigen ; T-Cell ; alpha-beta
Subject Areas:
Biology and Bio-materials
Instruments:
I03-Macromolecular Crystallography
Added On:
07/01/2013 14:43
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Technical Tags: