Cis-Prenyltransferases (cis-PTs) is a large enzyme family which is well conserved in all domains of life. Cis-PTs catalyze condensation reactions of isopentenyl pyrophosphate (IPP) and produce linear polyprenyl diphosphate. The length of this isoprenoid carbon chain varies from short molecules like geranyl diphosphate (C10) to natural rubber (C>10’000). The human cis-Prenyltransferase Complex (hcis-PT) has an essential role in protein N-glycosylation. It synthesises the precursor of glycosyl carrier dolichol-phosphate. Mutations in genes coding for hcis-PT can cause severe diseases, such as retinitis pigmentosa.[1]

Structure

The hcis-PT subunits

The hcis-PT is a tetramer formed by assembling a dimer of heterodimers. The hcis-PT is composed of two catalytically active dehydrodolichyl diphosphate synthases () and the Nogo-B receptor (). The NgBR can be divided into two domains a C-terminal pseudo prenyltransferase domain that interacts with DHDDS and an N-terminal transmembrane domain that is anchored in the endoplasmic reticulum. The NgBR C-terminus encompasses the RxG motif which might have an important role in hcis-PT activity and which is not present in NUS1 (6jcn), the yeast homolog of NgBR. The structure of DHDDS can be divided into three domains: (residues 251–333), an (residues 1–26) and a (residues 27–250). The cis-PT homology domain heterodimerizes with NgBR. The tetramer is formed by heterotypic interactions of the "turn" region with NgBR and by homotypic interactions between DHDDS. The whole complex is directed into the cytosol.

The active site organization

Farnesyl diphosphate (FPP) and Mg²⁺ are only detected in the active site of DHDDS and only the active site of DHDDS is required for the catalytic activity. NgBR induces an increase in the expression and activity of the complex but itself has no catalytic activity. In fact, NgBR active site does not have a visible substrate-binding cavity. The 3 β-strands and 2 α-helices are packed via hydrophobic interactions so there is no cavity anymore and it is devoid of water.

Catalytical activity of the human cis-prenyltransferases

The catalytical domain of DHDDS is homologous to undecaprenyl pyrophosphate synthase (UPPS) with 2 α-helices and four β-strands within each monomer. The active site is formed by a stabilizing the interaction between IPP and a which accommodate the elongating carbon chain. In the active-site, there are two substrate-binding sites, a S1 and a S2 site. The binds the initiatory substrate FPP. It also interacts with Mg²⁺ ions which are crucial for IPP hydrolysis during the condensation reaction. The Mg²⁺ is and stabilized. binds the IPP molecule which will be used for chain elongation. The C-terminus of NgBR (RxG) is directly involved in forming the superficial polar region and enable the formation of S1 and S2. In fact, at the S1 site, we have two polar interaction networks between NgBR and DHDDS. At , the backbone nitrogen atoms directly coordinate the phosphate molecule.

The elongation reaction in the hydrophobic active-site tunnel

The cis-PT catalyze the chain elongation of FPP by successive head-to-tail condensation with a specific number of IPP to form linear lipids with designated chain lengths. The reaction is as follows: IPP headgroups are bound to the enzyme at the superficial polar region while the carbon chains point toward the . First, the pyrophosphate group (FPP) of the initiatory substrate, which interacts with a Mg²⁺ ion, is hydrolyzed at the . Then, the condensation of remaining carbon with the IPP from S2 site follows. The elongated products translocate to the S1 so the carbon chain goes into the hydrophobic tunnel of the active site. At the end, a new IPP molecule binds to the S2 site and the cycle is repeated until the active site can no longer accommodate the long chain isoprenoid.

Regulation of the product length

The hydrophobic tunnel of DHDDS is formed by 2 α-helix and 4 β-strands. The opening between the 2 α-helices is larger in DHDDS compared to short and medium chain cis-PT. The larger the diameter, the better is the accommodation of longer product.

Functional importance and link to human health

Product of the N-glycosylation

The N-glycosylationis a post-translational modification realized in the endoplasmic reticulum of the cell. This process consist in linking a glycan to a protein, which provide the biological protein fonction and folding. The hcis-PT produce DHDD (dehydrodolichyl diphosphate), an important precursor molecule for the dolichol-phosphate lipid carrier needed in the N-glycosylation reaction.

Disease comprehension

The Retinitis pigmentosa is a hereditary disease. The patient loses progressively a part of his sight: Night vision as a teenager, side vision as a young adult and central vision in later life. This loss of sight is due to the progressive decrease of rod and cone photoreceptor cells which provide coloured vision. Scientists observed that symptoms appear many years after the beginning of the photoreceptor’s degeneration in most cases. Retinitis pigmentosa can be encoded by many genes. More than 45 have been identified but these genes concern only 60% of sick patients. Therefore 40% of cases of Retinitis pigmentosa are unidentified genes. Until today there is no cure. But studies showed a slow down of the disease with the intake of vitamin A palmitate foods and omega-3-rich fish [2].

For instance, missense mutations can provoke an autosomal recessive Retinitis pigmentosa (arRP). These mutations concern the S1 and S2 sites of the active site where pyrophosphate can bind and most of the mutations related to the disease impact directly the substrate binding, according to scientists. For one mutation, , it is more complicated. Scientists remarked that this mutation can associate itself with the other mutation via a salt bridge, which provokes in the protein scale, hypothetically, an interaction with the adjacent active-site residues positively charged. Experiments revealed the stable salt bridge between K42E and E234 but also another stable salt bridge with the residue. Finally, experiments proved that aberrant polar networks are due to the K42E mutation, disturbing the active-site residues which can’t interact with the substrate and leading to a decrease of the catalytic activity [1].