T Cell Receptor and the B Cell Receptor: Comparison

T stall Receptor and the B Cell Receptor ComparisonThe entire world is full of pathogens which we need to stir up off to leave a normal life. Due to this, we nurture an repellent system that services us fight off and prevent/manage posterior infections. Our tolerant system skunk be classified into two, the innate and acquired immune responses. The innate immune response is broadly particularised and wills the first vindicatory action against some(prenominal) infection. Their response to every subsequent infection stays the same as the initial infection. In contrast, the acquired immune response is exceedingly specific such that it provides defence by elementrating antibodies specific to an antigen. They excessively put on the capacity of keeping infection memory such that there ordain be a more powerful response to future infections. born(p) immune response is mostly provided by macrophages, dendritic electric cells, polymorphonuclear leukocytes, mast cells, natural grampus cells, erythrocytes and platelets. The acquired immune response is provided by lymphocytes, the T (T cells) and B lymphocytes (B cells).The lymphocytes are derived from hematogenic stem cells (HSC) in the bead marrow. That form MLPs (myeloid-lymphoid progenitors). If the HSC and MLP stay in the b champion marrow they form B cells and if they migrate (via blood) to the thymus they form T cells (see figure below).Initiation of immune response by the lymphocytes first considers realization of the antigens and this is achieved by cell surface receptors called BCRs (B cell receptor) and TCRs (T cell receptor). These two receptors generate great correspondingities and differences in their structure involvedes, antigen credit rating, cell energizing and cistrontic recombination.A) social organization OF BCRs AND TCRs both(prenominal) the BCR and TCR perplex great similarities and differences in the structure. They both exist as multi- arrange complexes as seen in the d iagrams belowi) Antigen recognition comp cardinalntsIn the figure above, persona A shows the structure of a BCR. The BCR antigen recognition medium is an immune gamma globulin (Ig) pinch (a transmembrane antibody). The antibody is modified via alternative splicing that adds a hydrophobic transmembrane domain and a short cytoplasmatic domain (3 aminoacids) at the C terminal of the immune globulin minacious chain (Wall Kuehl 1983). All nave B cells however express both IgM and IgD classes of immunoglobulin but do switch to former(a) classes upon activation by antigens (Goding, 1978). The antibody (figure 2C) is a highly specific Ig that empennage adopt any one of the 5 immunoglobulin isotopes, IgG, IgA, IgM, IgD and IgE. The antibody has 3 countrys of which 2 regions (FAB) vary from antibody to antibody and admit to antigens and 1 region (FC) that stick arounds to effector pinchs. The antibody is composed of 2 out of work and 2 heavy gyves held together by inter and int ra disulphide bonds. The heavy duress depending on the Ig iso lineaments can be any one of , , , or bonds. The variable domains (VH and VL) splice to antigen and also bring rough vari skill and antigen recognition specificity. This specificity is mainly due to the presence of 3 hypervariable regions (Complementary Determining Regions), namely CDR1, CDR2 and CDR3 in the variable regions. comparable to BCR, the antigen recognition medium in TCR is an immunoglobulin heterodimer make from and Ig chains (in most T cells) or and Ig chains. Un corresponding in BCRs where the IG can be of 5 types, in TCRs the Ig heterodimers are nevertheless of 2 types. The two Ig chains in TCRs are (also like BCRs) held together by intra and inter disulphide bonds. As seen in section C, all(prenominal) Ig chain folds into 2 domains, the variable and the constant domain. This folding greatly resembles the FAB region of the antibody in BCRs. Likewise antibodies, the and heterodimers also cons truct hypervariable regions (CDR1, CDR2 and CDR3) in variable domains. The variable regions in both BCRs and TCRs bring about specificity and diversenessThe BCR antibodies have a hinge joint (connecting FAB and FC) that hurls the Ig mote very flexible. Unlike antibodies, the flexibility of the TCR Ig molecule is very particular(a) at the elbow region (junction of constant and variable region) (Degano et al, 1996).ii) ACCESSORY PROTEINSBoth the BCR and TCR have very short cytoplasmic domains that restrict the screen of any bless transduction factors to the receptors. Due to this the receptors are unable to transducer signals into cells upon antigen recognition. Signal transduction is achieved via the assistant proteins. BCRs (figure 2 section A) accessory proteins consists of one or more dimmers of one distributively of Ig- and Ig- chains held together in the cell membrane by a pair of disulphide bonds. The cytoplasmic domains of these chains have phosphorylation sites called ITAMS. Unlike BCR accessory protein, the TCR accessory proteins (figure 2, section C) is composed of a complex know as CD3. It consists of 3 types of invariant chains, namely , and . A or chain couples up with one chain (by formation of disulphide bonds) each to form two dimmers ( and ). In rundown to this, a dimmer of 2 zeta () chains is also present. Together, these 3 dimers make up the CD3 complex. The chains have a much longer cytoplasmic tail than the , and chains and have 3 ITAMs as compared to one in the , and chains. Therefore for both BCR and TCR accessory proteins are dimmers that all contain ITAMs.B) times OF RECEPTOR DIVERSITYThere are millions antigens and we need to pee-pee millions of antibodies against them. However, we do non have millions of Ig genes so how are we able to produce all these different antibodies? The answer is antibodies are produced in developing B cells via genetic recombination of genes encoding the immunoglobulins (Hozumi and Tonegaw a, 1976). The figure below shows the gene segments coding immunoglobulins. trope legend The human heavy chain locus as shown in the last row, consists of about 38-46 functional VH genes, 27 DH and 6 JH genes. The wispy chain can be either made of or chains. The locus consists of about 30 functional V genes and 5 J genes each apart(p) by a J segments. The Kappa locus has about 34-40 functional V genes and 5 J genes.The variable heavy chain region of the antibody is made from the connecter of the V (variable), D (diversity) and J (joint) gene segments and the variable light chain (which can be either or ) is formed from the joining of V and J segments only. A process called V(D)J recombination involves joining different gene segments and as a result bringing about antibody diversity. At the heavy chain locus, any one of the 27 D and 6 J gene segments are first joined together and becausece any one of 46 V gene segment is joined to this DJ segment. This rearranged DNA is then transcribed to form a primary template RNA. This mRNA then affordes splicing to bring the VDJ segment close to the constant gene segment. Additional diversity is achieved as any 1 of the two types of light chains can be formed. Random insertion of nucleotides either nerve of D segments also creates N-nucleotide diversity. In total about 106 possible immunoglobulin gene combinations can be formed. This recombination process is driven by recombination signal grades that flank the coding gene segments. Certain enzymes (RAG-1 and RAG-2) help mediate this incarnate recombination process. The antibodies produce undergo a processs of clonal selectin where only the antibody specific to the antigen preferentially proliferates to make many antibodies.Binding affinity of BCR is greatly increased after(prenominal) antigen recognition where the variable regions of both heavy and light chain undergo somatic hypermutations. This is where point mutations are put in the variable regions of ra pidly proliferating B cells. These mutations produce antibodies that may have cracking, moderate or good affinity for the antigens. The antibody with good affinity will have a selective advantage during clonal selection.The gene segements encoding TCR chain follow the similar V,D,J and C arrangement of BCRs. The recombination process involves of of the two D genes rearranges next to one of J genes. Then one of the 50 V genes arranges next to the preformed DJ genes. As seen , this is also similar to the B cells where a DJ segement forms first and then joins up with a V segment. There is also random insertion, just like in B cells, of nucleotides either berth of D segments to create N-nucleotide diversity. Unlike in B cells, there is no somatic hypermutation in T cells after antigen recognition. If this occurs, the TCR will loose its ability to separate MHC and the peptide it presents.C) ANTIGEN BINDING/RECOGNITIONBCR and TCR have similar immunoglobulin antigen recognition recepto rs but the types of antigens they prize are very different. BCR can severalize nave (as a whole) antigens and TCR can only recognise a single antigen peptide sequence presented onto cell surfaces by MHC (Major histocompatibility complex) molecules. The antigens treasure by B cells are nave and therefore the antibody in BCR mostly recognise discontinuous epitopes on the antigen and antigens accepted by the TCR is in form of linear peptide sequences and therefore they mostly recognise continuous or linear epitopes.Antigen recognition by BCR is very unreserved where the antibody variable region simply recognises specific epitopes on antigen and bind to it. The BCR can recognise 3 types of antigens, Type 1 thymus independent antigens (where bacterial lipoproteins can bind to mitogenic bypass molecules on B cells surface and this allows non-specific antigen B cell activation), Type 2 thymus independent antigens (appiles to antigens that have swell spaced and repetitive polysacchari des that bind to multiple antibodies in BCR and activate the B cell) and Thymus dependent antigens (require helper T cells). Thymus dependent antigens when bind to TCR, instead of causing activation normally cause anergy. Due to this, erstwhile the binding has occurred, the whole antigen+TCR comples is endocytosed, the antigen is hydrolysed by enzymes and processed to small linear peptides and then presented onto the B cell surface via MHC2 molecules. Helper T cells then recognise this peptide-MHC complex. B cells have loads of CD40 on their surface that binds to CD40L present on Th helper cells. In response to this Th cells secrete IL-4, 5, 6 that also help activate other costimulatory molecules in the BCR coreceptor complex. All these events provide costimulation of the B cells and it is activated. heterodimer TCRs in comparison can recognise any type of antigen that is processed and presented as a single peptide on MHC1 on fool cells and MHC2 on B cells, macrophages and dendrit ic cells (all professional antigen presenting cells). The non-covalent forces that help TCR bind to the peptide-MHC complex are similar to the forces that enable the antibody bond to the antigen i.e. noncovalent.Unlike BCR that only have to recognise epitopes on antigens, the TCR has to both recognise the presence of both MHC molecule and antigen peptide. The TCR V (variable alpha region) overlays 2 scroll of MHC1 or 1 helix of MHC2 and the V domain overlays 1 helix in both MHC1/2. The CDR1 and CDR2 bind to helices of MHC and the CDR3 (which is more variable), binds to the antigen peptide on MHC. This concept is summarised in the picture below attribute legend The picture shows how the TCR variable complementarity determining regions (CDR) which are the binding sites interact with peptide-MHC complex. The CDR1 and CDR2 bind to the MHC alpha helices and CFR3 binds to the peptide.The TCRs are more similar to BCR antibody as they can recognise nave antigens without the requirement o f processed antigen presentation. Another similarity of BCR and TCRs is that in the antibodies of BCRs, the CDR3 regions on heavy chain are shorter than the CDR3 in heavy chains and also the same in TCRs is seen where the are shorter than the CD3.COSTIMULATIONSBoth lymphocytes do not get activated (but undergo anergy) once they recognise and bind to an antigen. They require costimulatory signals that will eventually lead to the activation of the lymphocytes. The B cells have BCR co receptor complex consisting of CD19 and CD21 (complement receptor), CD81 and LEU13 (interferon induced transmembrane protein 1). All these molecules are stimulated in presence of interferons and complements that give a costimulatory signal to B cells and activate it when it has recognised an antigen. The precise details of how these costimulatory molecules stimulate B cell signalling are tranquillize under investigation.In contrast to the 4 main costimulatory molecules in B cells, the primary costimu latory molecule in T cells is CD28 (figure besides)The binding of peptide-MHC to TCR causes up-regulation of certain molecules (e.g. CD28). T cells, like B cells can be costimulated by either cytokines or costimulatory molecule interactions.APC have surface molecules such as the B7.1 and B7.2 (or the CD80 and CD86) that recognise and bind to a molecule on the surface of the T cells called CD28 frame on CD. This interacting provides co stimulation. The CTLA4 molecule is highly expressed after proliferation of the T cells. Once it binds to B7, instead of co stimulating T cells, it turns the T cells off. This is ministrant in preventing excessive immune responses. No such regulatory instrument is seen in B cells.A unique feature of T cells is that they have co receptors (CD4 and CD8) that help recognise the MHC molecules. CD4 molecules act as co receptors for MHC2 and are found on helper T cells and CD8 molecules present on cytotoxic T cells help recognise MHC1 molecules.ACTIVATION OF B AND T CELLSThe activation of B and T cells following antigen recognition is somehow similar as it involves the phosphorylation of the ITAMS of accessory proteins. In B cells, antigen binding and co stimulation recruits the BCR+antigen to lipoid lots that brings protein tyrosine kinase Lyn close to the ITAMs of the cytoplasmic tails of the BCR associated proteins. Lyn phosphorylates ITAMs and triggers a signal cascade down that results in increase of cytoplasmic calcium levels that activate transcription factors that image the entry of B cells into cell cycle. Eventually activate the B cells which then form plasma cells (that make loads of clones of antibodies to the antigen) and memory cells that will help manage subsequent infections. The initial proliferation of the activated B cell is tended to(p) by somatic hypermutation of the rearranged antibody variable genes that lead to the production of antibodies that may have poor, moderate or good binding capacity to the antig en. The good binding antibodies will be preferentially selected during clonal selection and they will kick upstairs undergo proliferation to produce plasma and memory cells.A similar particular also occurs in T cells where there is activation of lipid rafts that bring the zeta chain ITAMS close to Lck (a protein tyrosine kinase) that phosphorylates the ITAMs and therefore create opportunity for other factors to bind to it and eventually cause mobilization of calcium that causes proliferation of T cell into Helper T cells, Regulatory T cells and Cytotoxic T cells.