Receptor tyrosine kinases (RTKs) are part of the larger family of protein tyrosine kinases. They are the high-affinity cell surface receptors for many polypeptide growth factors, cytokines, and hormones. Approximately 20 different RTK classes have been identified.[1]
Lapatinib is a EGFR inhibitor used in breast cancer treatment. ERBB2 is necessary for heart cells proliferation and regeneration[2].
Epidermal Growth Factor Receptors are overexpressed in many types of human carcinomas including lung, pancreatic, and breast cancer, and are often mutated. This overexpression leads to excessive activation of the anti-apoptotic Ras signalling cascade, resulting in uncontrolled DNA synthesis and cell proliferation. Studies have revealed that the is responsible for activating this Ras signaling cascade. Upon binding ligands like Epidermal Growth Factor, EGFR dimerizes and autophosphorylates several tyrosine residues at its C-terminal domain. Upon phosphorylation, EGFR undergoes a significant conformational shift, revealing an additional binding site capable of binding and activating downstream signaling proteins.[3] Erlotinib inhibits the EGFR tyrosine kinase by located within the kinase domain. Residues Met 774, Leu 825, Val 707, Thr 835, Asp 836, Phe 837, Thr 771, Lys 726, Ala 724, & Leu 769 tightly bind the inhibitor in place. Unable to bind ATP, EGFR is incapable of autophosphorylating its C-terminal tyrosines, and the uncontrolled cell-proliferation signal is terminated.[4]
Gefitinib inhibits the EGFR by located within the kinase domain. Residues Lys 745, Leu 788, Ala 743, Thr 790, Gln 791, Met 193, Pro 794, Gly 796, Asp 800, Ser 719, Glu 762, & Met 766 tightly bind the inhibitor. Unable to bind ATP, EGFR is incapable of autophosphorylating its C-terminal tyrosines, and the uncontrolled cell-proliferation signal is terminated.[5]
Erlotinib inhibits the EGFR by located within the kinase domain. EGFR uses residues Asp 831, Lys 721, Thr 766, Leu 820, Gly 772, Phe 771, Leu 694, Pro 770, Met 769, Leu 768, Gln 767 & Ala 719 to tightly bind the inhibitor. Unable to bind ATP, EGFR is incapable of autophosphorylating its C-terminal tyrosines, and the uncontrolled cell-proliferation signal is terminated.[6]
A Possible Strategy against Head and Neck Cancer: In Silico. Investigation of Three-in-One inhibitors[7]
(in darkmagenta), which is an enzyme with decarboxylation reaction of uroporphyrinogen III to (in salmon), is overexpressed in tumor tissues and has potential to sensitize cancer patients to radiotherapy. Moreover, (in magenta) and (in deeppink), which are tyrosine kinase receptors in the erbB family, are also overexpressed in tumor tissues and have been indicated as the important targets of therapy for cancer. In this research, we discuss the possible conformation for an inhibitor against three target proteins, UROD, EGFR, and Her2.
Virtual screening of the UROD (PDB ID: 1r3y), EGFR (PDB ID: 3poz), and Her2 (PDB ID: 3pp0) was conducted using the binding site defined by the volume and location of the co-crystallized compounds in each crystal structure. In silico results indicate the traditional Chinese medicine (TCM) compounds had high binding affinity with all 3 target proteins. For (in magenta), the top 3 compounds, (in yellow), (in cyan), and (in orange), formed hydrogen bonds with the residues, Arg803, Lys913 and some other residues in the binding domain. The docking poses of (in deeppink) with (in yellow), (in cyan<), and (in orange), exhibited hydrogen bonds between ligands and the residues in the binding site. For protein (in darkmagenta), (in yellow), (in cyan), and (in orange), have hydrogen bonds with the 3 important binding and catalytic residues Arg37, Arg41, Tyr164, and the residue His220. The 3 TCM compounds hint towards a probable molecule backbone which might be used to evolve drug-like compounds against EGFR, Her2, and UROD, and have potential application against head and neck cancer.
See also Herceptin - Mechanism of Action
Insulin receptor
The insulin receptor (IR) is a dimer of made of 2 and 2 . Within the extracellular ectodomain, there are 4 potential that can interact with insulin on the extracellular side of the membrane. The full extracellular and intracellular components of the IR have only been imaged in separate sections but a larger picture of how these sections combine to initiate downstream tyrosine autophosphorylation is emerging.
The make up the extracellular domain of the IR and are the sites of insulin binding. The α-subunit is comprised of 2 Leucine rich domains (L1 & L2), a Cysteine rich domain (CR), and a . α-CT has a unique position that allows it to reach across the receptor and interact with the insulin at the binding site on the opposing side of the receptor. The α-subunits are held together by a disulfide bond between on each α-subunit. The disulfide bonds are important to the overall stabilization of the molecule as it binds to insulin. Two types of insulin binding sites are present in the α-subunits, and . The sites are in pairs because of the heterodimeric nature of the receptor. Due to structural differences, as well as greater surface area and accessibility, binding sites 1 and 1' have much higher affinity for insulin binding than sites 2 and 2'. Insulin can also bind at sites 2 and 2', but the location on the back of the beta sheet of the FnIII-1 domain and lack of surface area decreases the likelihood of their binding site becoming occupied as quickly.
The spans from the extracellular domain across the TM region and into the intracellular portion of the IR. The β-subunit is composed of part of fibronectin domain III-2 and all of Fibronectin domain III-3. The β-subunit's FnIII-3 domain has links through the TM region into the intracellular part of the membrane. Cryo-EM provided clear representations of the FnIII-2 and FnIII-3 domains, but are missing the TM and intracellular regions. Although the FnIII-3 domain is connected to the TM and intracellular regions, the active conformation likely extends all the way to the tyrosine kinase domain region (4xlv).
The α and β subunits of the extracellular domains fold over one another and form a when the IR is inactivated. Upon activation, the extracellular domain undergoes a conformational change and forms a . An additional component to the ectodomain is . Each of the dimers has an α-CT helix. The α-CT helix is a single α-helix that plays an important role in insulin binding and stabilization of the "T" shape activated conformation. α-CT interacts with a leucine-rich region of the α subunit and a fibronectin type III region of the β subunit to form the insulin binding sites known as .
The structure of the extracellular domain is stabilized through multiple disulfide bonds. The α-subunits are linked through 2 disulfide bonds, with the main one being between of 2 adjacent α-subunits. of both α-subunits are also held together with a disulfide bond. The α-subunit is also attached to the β-subunit by a disulfide bond between the . The IR unit has 4 separate sites for the insulin binding. There are 2 pairs of 2 identical binding sites referred to as and .
The insulin molecules bind to these sites mostly through hydrophobic interactions, with some of the most crucial residues at sites 1 and 1' being between of the IR FnIII-1 domain. Despite some of the residues included being charged, the main interactions are still hydrophobic in this binding site. For example, due to arginine carrying its positive charge at the end of the side chain, to allow the hydrophobic part of the side chain to interact with the other hydrophobic residues. The α-subunits also have significant that help maintain a compact binging site. At sites 2 and 2', the major residues contributing to these hydrophobic interactions are the .
Sites 1 and 1' have a higher binding affinity than sites 2 and 2' due to site 1 having a larger surface area (706 Å2) exposed for insulin to bind to compared to site 2 (394 Å2). The binding interactions of the insulin molecules in sites 1 and 1' are facilitated by hydrophobic residues of an of the IR. The insulin molecules in sites 2 and 2' primarily interact with the residues that comprise some of the of the IR.
At , a occurs between 3 critical parts of the α subunits of the IR. The entire interface of the tripartite interaction involves many residues that are involved with intra-protomer ionic and hydrogen bonding at the binding site. The α-CT chain and the FnIII-1 domain region come into close proximity during the conformational change of the IR and their interaction involves the following residues: and the . This duo then interacts with the L1 region, specifically ARG14, creating an ideal for the insulin ligand. The FnIII-1 and α-CT are interacting from the 2 different α-subunits, which displays a "cross linking" scenario where the domains of the heterodimer can intertwine with each other. The tripartite interaction between α-CT, the FnIII-1 domain, and the L1 region is important because it allows for a strong interaction between 2 subunits of the IR that maintains and stabilizes the T-shape activation state for the rest of the downstream signaling to occur.
It has been hypothesized that activation of the IR can change based on the concentration of insulin. These structures of the IR have demonstrated that at least 3 insulin molecules have to bind to the IR to induce the active conformation, as binding of 2 insulin molecules is insufficient to induce a full conformational change. However, this conclusion has not yet been widely confirmed. In low concentrations of insulin, the IR may not require binding of 3 insulin molecules in order to exhibit activation. Rather, the level of activity will change in accordance to the availability of insulin. When higher concentrations of insulin are present, the conformational difference between the 2-insulin-bound state and the 3-insulin-bound state is drastic as the IR transitions from the inactive to the active . However, in conditions of low insulin availability, the 2-insulin-bound state may be enough to induce partial activation of the receptor.
The conformational change between the inverted, inactive and the active of the IR is induced by insulin binding. The T shape conformation is well observed in the α subunit. It is horizontally composed of L1, CR (including the ), and L2 domains and vertically composed of the FnIII-1, 2, and 3 domains. The proper conformational change of the ectodomain of the IR is crucial for transmitting the signal into the cell. The movements extracellularly cause the 2 receptor tyrosine kinase domains intracellularly to become close enough to each other to autophosphorylate. This autophosphorylation activates the tyrosine kinase domain, initiating intracellular insulin signaling cascades.
When an insulin molecule binds to site 1 of the α-subunit, the respective protomer is recruited and a slight inward movement of the of the β-subunit is initiated. This is accomplished by the formation of several salt bridges, specifically between . Binding of insulin to both protomers establishes a full activation of the IR. This activation is demonstrated through the inward movement of both protomers. This motion has been referred to as a "hinge" motion as both protomers "swing" in towards one another. The conformational change and "hinge motion" between the inactive and active forms of an IR protomer. Upon insulin binding, the β subunits of the inactive form, shown in blue, are "swung" inward to the active form, shown in orange. When the receptor is in an , the FnIII-3 domains are separated by about 120Å. This distance prevents the initiation of autophosphorylation and downstream signaling by the tyrosine kinase domains on the intracellular side of the receptor. Upon the binding of insulin to multiple binding sites, this conformation change brings the FnIII-3 domains within 40Å of each other to induce the conformation. As the fibronectin type III domains of the β subunit swing inward, the α subunits also undergo a conformational change upon insulin binding. As insulin binds to site 1, the leucine-rich region of one protomer interacts with α-CT and the FNIII-1 domains of the other protomer to form the binding site. For the tripartite interface to form, the α subunits of each protomer must undergo a "folding" motion.
(3bu5).
TK domain of IR contains an activation loop and a catalytic loop and . The bound IR substrate 2 peptide tyrosine is the phosphorylated residue[8].
In type 2 diabetes, the TK domain is thought to be down-regulated through phosphorylation of by protein kinase C[9].
. Water molecules shown as red spheres.
Student Projects for UMass Chemistry 423 Spring 2012-1
The crystallized protein, shown here, is the of the IR, as it is difficult to crystallize the protein and determine the structure when the greasy TM portion of the protein is included. Four FAB antibodies (shown in peach, yellow, light green, and light blue) are attached to the protein to aid in crystallization. The IR is to the membrane at the β strand, which extends through the cell membrane. The receptor is attached to the cell membrane by the β strand, which extends through the membrane and into the interior of the cell and mediates activity by the addition of phosphate to tyrosines on specific proteins in cell. In humans, correctly functioning IRs are essential for maintaining glucose levels in the blood. The IR also has role in growth and development (through insulin growth factor II); studies have shown that signalling through IGF2 plays a role in the mediation embryonic growth. In everyday function, insulin binding leads to increase in the high-affinity glucose transporter (Glut4) molecules on the outer membrane of the cell in muscle and adipose tissue. Glut4 mediates the transport of glucose into the cell, so an increase in Glut4 leads to increased glucose uptake. Insulin has 2 different receptor-binding surfaces on opposite sides of the molecule, that interact with 2 different . The 1st binding insulin surface interacts with a site on the L1 module as well as a 120-amino-acid peptide from the insert in FnIII-2'. The 2nd binding site consists of residues on the C-terminal portion of L2 and in the FnIII-1 and FnIII-2 modules. Binding sites are shown highlighted in both monomers of the biologically functional dimer.
The ectodomain of the IR is a of 2 identical monomers. Each v-shaped is composed of 6 domains, 3 on each side of the V, shown in different colors. The red (L1) is involved in substrate binding. Its main feature is a 6 parallel stranded β sheets. The orange (CR) is composed mostly of loops and turns. The yellow domain is a 2nd , (L2) which contains a 5 parallel stranded β sheets and several surface α helices. The next 3 domains are Fibronectin Type III domains. Fibronectin domains, characterized by β sandwiches, are named after the protein fibronectin, which contains 16 of these domains. The green FnIII-1 , contains one antiparallel and one mixed β sheet. The blue FnIII-2 contains an insert domain of 120 residues. The purple FnIII-3 contains just 4 β strands. Each domain occurs twice in the . The insert domain of the FnIII-2 domain separates the α and β chains of each monomer. The α chain contains the L1<, CR, L2, FnIII-1 domains and part of the FnIII-2 domain. The β chain contains the rest of the FnIII-2 domain and the FnIII-3 domain. The insert domain starts and ends with a cleavage site where the chain is cut. The α and β chains are then linked by a single between cysteines C647 and C860, leaving the insert domain as a separate peptide which forms disulphide bonds with cysteines in the FnIII-1 domain. The α chain lies completely on the exterior of the cell, while the end of the β chain extends through the cell membrane and is involved in signaling. This section of the β chain, after the FnIII-3 domain in the sequence, is not shown in the structure which reflects only the . There are few interactions between the 2 legs of the monomer - just 2 salt bridges near the connection between the L2 and FnIII-1 domains. However, there are many interactions between the two monomers including salt bridges and disulphide bonds. This structure is significant relative to previous structures for the protein because of the relative position of the L1 domains in the 2 monomers of the biological unit. In previously proposed structures, the L2, CR, and L1 domains formed a straight leg of the V similar to that of the fibronectin leg. With this model, it was thought that both L1 domains could bind to a single insulin molecule. With this folded over structure of the L2-CR-L1 leg, it is clear that this is not the case, as the L1 domains of each monomer face away from each other.
In order to better understand the binding of the IR, it would make sense to observe its main ligand, . This scene shows both the hydrophobic (in gray) and hydrophilic residues (in magenta). The binding surface is mostly comprised of residues that are hydrophobic.
The insulin in its can also interact with the binding sites available on the IR. Hexamers of insulin are found in the pancreas and help store insulin. They consist of 3 insulin dimers that are held together by 2 Zn ions. Upon creating the hexamer form, a new binding surface for insulin is created that exhibits normal binding at site 1. Binding does not occur at site 2 however, and thus the hexamer form of insulin does not activate the IR as does regular form of insulin. Here is a that highlights the 2nd binding surface. The 2nd binding surface is highlighted on 1 of the 3 dimers and involves a small group of specific residues: SerA12, LeuA13, GluA17, HisB10, GluB13, and LeuB17.
Extensive research has been conducted to see if the IRs can bind to other proteins which can then induce the kinase cascade pathway. In one experiment, the within the IRs has shown to exhibit binding to the active sites of the IRs. It does so through what has been hypothesized to be between the 2 monomers in the homodimer. The actual peptide connecting one piece of the insert domain to the other has yet to be resolved, however the binding portion of the insert domain has been to be at Site 1, between the L1 and FnIII-2 domains. Since insulin binds to Site 1 as well, it is also hypothesized that the binding portion of the insert domain competitively binds with the insulin protein because of its mimical structure to insulin. This is quite an important discovery, because a compound that can mimic the structure of insulin could have a higher affinity for the IRs, which could activate the signal transduction pathway.
Vascular Endothelial Growth Factor Receptors (VEGFRs) are tyrosine kinase receptors responsible for binding with VEGF to initiate signal cascades that stimulate angiogenesis among other effects. The tyrosine kinase domain of VEGFR-2 is separated into 2 segments with a 70 amino acid long kinase insert region. Upon binding VEGFA and subsequent dimerization, VEGFR-2 is autophosphoryalted at the carboxy terminal tail and kinase insert region, 6 tyrosine residues of VEGFR2 are autophosphorylated. within the activation loop of VEGFR2 leads to increased kinase activity. (3c7q).
See also Bevacizumab.
