TY - JOUR
T1 - A step-by-step overview of the dynamic process of epitope selection by major histocompatibility complex class II for presentation to helper T cells [version 1; referees
T2 - 4 approved]
AU - Sadegh-Nasseri, Scheherazade
N1 - Publisher Copyright:
© 2016 Sadegh-Nasseri S.
PY - 2016
Y1 - 2016
N2 - T cell antigen receptors (TCRs) expressed on cytotoxic or helper T cells can only see their specific target antigen as short sequences of peptides bound to the groove of proteins of major histocompatibility complex (MHC) class I, and class II respectively. In addition to the many steps, several participating proteins, and multiple cellular compartments involved in the processing of antigens, the MHC structure, with its dynamic and flexible groove, has perfectly evolved as the underlying instrument for epitope selection. In this review, I have taken a step-by-step, and rather historical, view to describe antigen processing and determinant selection, as we understand it today, all based on decades of intense research by hundreds of laboratories.
AB - T cell antigen receptors (TCRs) expressed on cytotoxic or helper T cells can only see their specific target antigen as short sequences of peptides bound to the groove of proteins of major histocompatibility complex (MHC) class I, and class II respectively. In addition to the many steps, several participating proteins, and multiple cellular compartments involved in the processing of antigens, the MHC structure, with its dynamic and flexible groove, has perfectly evolved as the underlying instrument for epitope selection. In this review, I have taken a step-by-step, and rather historical, view to describe antigen processing and determinant selection, as we understand it today, all based on decades of intense research by hundreds of laboratories.
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U2 - 10.12688/F1000RESEARCH.7664.1
DO - 10.12688/F1000RESEARCH.7664.1
M3 - Review article
AN - SCOPUS:85010866377
SN - 2046-1402
VL - 5
JO - F1000Research
JF - F1000Research
M1 - 1305
ER -