Glycoprotein Ib-IX-V Receptor Complex


The GPIb-IX-V complex is a profuse membrane receptor complex originating in megakaryocytes and exclusively functional on the surface of platelets. It primarily functions to mediate the first critical step in platelet adhesion, by facilitating binding to von Willebrand factor on damaged sub-endothelium under conditions of high fluid shear stress. Although the primary ligand for the GPIb-V-IX receptor is VWF, it can also bind to a number of other ligands in the circulation such as thrombin, P-selectin, factor XI, factor XII, high molecular weight kininogen as well as bacteria. GPIb-IX-V offers a critical role in thrombosis, metastasis, and the life cycle of platelets, and is implicated in a number of thrombotic pathological processes such as stroke or myocardial infarction.

Molecular structure

Overview

GPIb-IX-V consists of four different subunits namely: GPIbα, GPIbβ, GPIX and GPV. The complex is assembled such that GPIbα, GPIbβ and GPIX form a highly integrated protein complex in a 1:2:1 stoichiometry; and this associates weakly with GPV resulting in an overall stoichiometric ratio of 1:1.
Each subunit of the complex is a type I transmembrane protein which consists of a leucine-rich repeat ectodomain, a single transmembrane helix, and a relatively short cytoplasmic tail that lacks enzymatic activity.
The quaternary stabilization of the receptor is facilitated by covalent and non-covalent interactions. The GPIbα subunit is linked to two GPIbβ subunits via membrane-proximal disulfide bonds, while GPIX associates itself tightly through non-covalent interactions with GPIb. The concomitant expression of all three subunits is required to allow the effective expression of GPIb-IX on the platelet cell surface and analysis of receptor expression in transfected Chinese hamster ovary cells has further supported that the interaction between these subunits also acts to stabilize them.
s between GPIbα and GPIbβ.
Each of the four subunits is part of the leucine rich repeat motif superfamily. These leucine rich repeat sequences tend to be about 24 amino acids in length either occurring singly or in tandem repeats flanked by conserved N-terminal and C-terminal disulfide loop structures. Nevertheless, even though these structural similarities exist, distinctive genes that exist on different chromosomes of the genome code for the polypeptides that make up the GPIb-V-IX complex.
The four genes that code for the components of the receptor in humans have a simple organization in which the coding sequence is contained within a single exon. This is with the exception of the gene for GPIbβ, which contains an intron 10 bases following the start codon.
Human GPIbα is the product of a gene on chromosome 17 specifically 17p12, GPIbβ is the product of a gene on chromosome 22 specifically 22q11.2, while GPV and GPIX are products of genes found on chromosome 3 specifically 3q21 and 3q29 respectively. Under normal conditions, all four molecules are expressed exclusively in the platelet lineage. GPIbα, GPIbβ and GPIX are necessary for the effective biosynthesis of the receptor and are closely associated at the platelet membrane. Typically, a lack of a single subunit significantly decreases the surface expression of the entire receptor complex.

GPIbα

consisting of 610 amino acids is the major subunit and contains all known extracellular ligand-binding sites of the complex for example: the A1 domain of von Willebrand factor has a binding region as marked in the N-terminal domain of GPIbα; while the thrombin binding site is contained in a conformationally flexible acidic residue-rich sequence containing sulfated tyrosines.
depicting the various components of the GPIbα subunit.
Dissection of the crystal structure of the GPIbα N-terminal leucine rich repeat domain discloses the presence of a single disulfide bond between cysteine residues Cys4 and Cys17 in the N-capping region, and two disulfide bonds in the C-capping region. Furthermore, there are seven tandem leucine rich repeats and their flanking sequences in the central parallel β-coil region. This parallel β-coil region is made up of three sided coils stacked in layers and contains two asparagine residues, which serve as N-glycosylation sites. Following the leucine rich repeat domain is the acidic residue-rich sequence containing sulfated tyrosines, the highly O-glycosylated macroglycopeptide, a stalk region of about 40 to 50 residues, a single transmembrane sequence and finally a cytoplasmic tail containing 96 amino acid residues which includes serine residues such as Ser587, Ser590 and Ser609 that can be phosphorylated.

GPIbβ, GPIX, GPV

contains 181 amino acids. In the extracellular domain, both the N-capping and C-capping regions, which flank the leucine rich repeat sequence, contain two interlocking disulfide bonds. Furthermore, there is only a single leucine-rich repeat giving rise to a much less curved parallel β-coil region as compared to that in GPIbα. GPIbβ contains only one N-glycosylation site and is disulfide linked to GPIbα immediately proximal to the plasma membrane of the platelet via Cys122 located at the junction of the extracellular and transmembrane domains.
depicting the crystal structure of the GPIbβ extracellular domain. The N-terminus is positioned at the top, the concave β-strands sit to the right and the convex loops are positioned to the left. Disulfide bonds present in LRR regions are indicated in yellow.
The GPIbβ cytoplasmic domain has a sequence of 34 amino acids. The region adjacent to the membrane is enriched in basic residues and Ser166 found more distally is phosphorylated and appears to have a role in platelet cytoskeletal rearrangement.
GPIX contains 160 amino acids. The extracellular domain, which also only has a single leucine rich repeat sequence shares more than 45% sequence identity with GPIbβ counterpart. However, the transmembrane and cytoplasmic sequences are considerably different. The GPIX cytoplasmic tail is short consisting of 8 residues and is not known to associate with intracellular proteins. There is also a cysteine residue located at the junction of the transmembrane and cytoplasmic domains. The extracellular domain of GPV contains 13 leucine rich repeats flanked by N- and C- capping regions both containing two interlocking disulfide bonds. This is followed by a stalk region, the transmembrane sequence and a short cytoplasmic tail rich in basic residues.
The GPV subunit is only weakly associated with the GPIb-IX part of the receptor complex through interactions between the transmembrane domains and has little impact on the surface expression of GPIb-IX, although GPIb-IX is required for efficient expression of GPV. Furthermore, GPV doesn’t appear to be critical for VWF binding or signal transduction.

Role in disease

Abnormalities of the GPIb-V-IX complex result in abnormal appearance and functioning of platelets resulting in Bernard–Soulier syndrome, a condition first described by Bernard J and Soulier J.P. It is a rare hereditary bleeding disorder most commonly with an autosomal recessive inheritance and diagnosed based on prolonged skin-bleeding time, a reduced number of very large platelets and defective ristocetin-induced platelet agglutination.
Bernard Soulier Syndrome is characterized by little or no expression of GPIb-IX on the surface of platelets which in turn has the same effect on GPV. There have been a number of mutations associated with BSS patients that have been mapped to GPIbα, GPIbβ and GPIX demonstrating that all three subunits are required for effective surface expression of the complex on platelets.