نتایج جستجو برای: tapasin

تعداد نتایج: 263  

2002
Toshio Yabe Sumiyo Kawamura Masako Sato Koichi Kashiwase Hidenori Tanaka Yoshihide Ishikawa Yoji Asao Junko Oyama Kazuma Tsuruta Katsushi Tokunaga Kenji Tadokoro Takeo Juji

HLA class I expression depends on the formation of a peptide-loading complex composed of class I heavy chain; 2microglobulin; the transporter associated with antigen processing (TAP); and tapasin, which links TAP to the heavy chain. Defects in TAP result in a class I deficiency called the type I bare lymphocyte syndrome (BLS). In the present study, we examined a subject with a novel type I BLS ...

Journal: :Poultry science 2006
L Sironi B Lazzari P Ramelli C Gorni P Mariani

Tapasin is a transmembrane glycoprotein located in the endoplasmic reticulum. Its function is to assist the assembly of major histocompatibility complex class I molecules. The chicken Tapasin gene includes 8 exons and is localized inside the major histocompatibility complex between the 2 class IIbeta genes. The aim of the current study was the estimation of single nucleotide polymorphism freque...

Journal: :FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2012
Sabine Hulpke Christoph Baldauf Robert Tampé

The loading of antigen-derived peptides onto MHC class I molecules for presentation to cytotoxic T cells is a key process in adaptive immune defense. Loading of MHC I is achieved by a sophisticated machinery, the peptide-loading complex (PLC), which is organized around the transporter associated with antigen processing (TAP) with the help of several auxiliary proteins. As an essential adapter p...

Journal: :Journal of immunology 1999
W K Suh M A Derby M F Cohen-Doyle G J Schoenhals K Früh J A Berzofsky D B Williams

In human cells the association of MHC class I molecules with TAP is thought to be mediated by a third protein termed tapasin. We now show that tapasin is present in murine TAP-class I complexes as well. Furthermore, we demonstrate that a mutant H-2Dd molecule that does not interact with TAP due to a Glu to Lys mutation at residue 222 of the H chain (Dd(E222K)) also fails to bind to tapasin. Thi...

Journal: :Journal of immunology 2014
Syed Monem Rizvi Nasir Salam Jie Geng Ying Qi Jay H Bream Priya Duggal Shehnaz K Hussain Jeremy Martinson Steven M Wolinsky Mary Carrington Malini Raghavan

MHC class I polymorphisms are known to influence outcomes in a number of infectious diseases, cancers, and inflammatory diseases. Human MHC class I H chains are encoded by the HLA-A, HLA-B, and HLA-C genes. These genes are highly polymorphic, with the HLA-B locus being the most variable. Each HLA class I protein binds to a distinct set of peptide Ags, which are presented to CD8(+) T cells. HLA-...

Journal: :European journal of immunology 2008
Stephen M Thirdborough Joanne S Roddick Joanna N Radcliffe Mark Howarth Freda K Stevenson Tim Elliott

Peptide loading of MHC class I molecules involves multiple cofactors including tapasin. We showed previously in vitro that tapasin edits the peptide repertoire by favoring the binding of peptides with slow dissociation rates. Here, using tapasin-deficient mice and a DNA vaccine that primes directly, we confirm that tapasin establishes hierarchical responses in vivo according to peptide-MHC stab...

2017
Olivier Fisette Sebastian Wingbermühle Lars V. Schäfer

Antigen processing on MHCI involves the exchange of low-affinity peptides by high-affinity, immunodominant ones. This peptide editing process is mediated by tapasin and ERAAP at the peptide C- and N-terminus, respectively. Since tapasin does not contact the peptide directly, a sensing mechanism involving conformational changes likely allows tapasin to distinguish antigen-loaded MHCI molecules f...

Journal: :Journal of immunology 2006
Verónica Montserrat Begoña Galocha Miguel Marcilla Miriam Vázquez José A López de Castro

B*2704 is strongly associated to ankylosing spondylitis in Asian populations. It differs from the main HLA-B27 allotype, B*2705, in three amino acid changes. We analyzed the influence of tapasin, TAP, and immunoproteasome induction on maturation, surface expression, and T cell allorecognition of B*2704 and compared some of these features with B*2705 and B*2706, allotypes not associated to disea...

Journal: :Journal of immunology 2006
Vilasack Thammavongsa Gayatri Raghuraman Tracy M Filzen Kathleen L Collins Malini Raghavan

A single residue polymorphism distinguishes HLA-B*4402(D116) from HLA-B*4405(Y116), which was suggested to allow HLA-B*4405 to acquire peptides without binding to tapasin-TAP complexes. We show that HLA-B*4405 is not inherently unable to associate with tapasin-TAP complexes. Under conditions of peptide deficiency, both allotypes bound efficiently to TAP and tapasin, and furthermore, random nona...

Journal: :Journal of reproductive immunology 2008
Paula W Lampton Carmit Y Goldstein Carol M Warner

Preimplantation mouse embryos express both classical (class Ia) and nonclassical (class Ib) MHC class I proteins, and yet are not rejected by the maternal immune system. Although the function of the embryonic MHC class Ia proteins is unknown, one MHC class Ib protein, Qa-2, the product of the preimplantation embryo development (Ped) gene, actually enhances reproductive success. Similar in struc...

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