RAB2B

RAB2B is a human protein whose gene is located in the fourteenth chromosome. It has a core made of basic elements such as oxygen, carbon, nitrogen and phosphorus. Its secondary structure contains eight alpha helix and six beta strands. Moreover, it has attached a magnesium ion and a GDP.[6]

Mature RAB2B contains three post-translational modifications, a phosphoserine is found in the location 202 instead of a normal serine, and two lipidations can be found in locations 215-216. It has a motif domain between the amino acids 35 and 43.

Due to the alternative splicing, two isoforms of this same protein exist. Isoform 1 is the canonical sequence, meaning it is the most common one, having a molecular weight of 24,214 Da.[7] Isoform 2 consists just of 151 amino acids, having a mass of 16,667 Da.

Small GTPases of the RAB superfamily are recognized as key players of the protein machinery involved in vesicular transport[8] and organelle dynamics in eukaryotic cells. RAB2B follows mainly exocytic pathways, from the endoplasmic reticulum to Golgi complex. RAB proteins are involved in docking and fusion of transport vesicles with their target membranes. These proteins associate with effector proteins (GARIL4 and GARIL5) to create complexes.

Representation of how RAB2B acts during an antiviral response and the elements it interacts with

In order to do its biological function, RAB2B has to switch from the GDP form to the GTP form, and this is possible thanks to the catalysation of GEF proteins, which are guanine exchange factors. On the other hand, when RAB2B are inactive in the cytosol, the GDP form is maintained due to the interaction with GDI proteins, which are GDP dissociation proteins.[9]

Studies have also shown that RAB2B affects the IFN antiviral response which is induced by cytosolic DNA. Because of this, RAB2B deficiency allows for vaccinia virus to replicate itself. After DNA stimulation, RAB2B attaches itself on the Golgi apparatus, along with stimulator of interferon genes (STING), the downstream signal mediator of cGAS. In order for RAB2B to adhere to the Golgi apparatus, RAB2B’s GTP-binding activity is required, as well as for the recruitment of GARIL5, so the RAB2B-GARIL5 complex can be formed. It is also shown that GARIL5 deficiency affects the IFN antiviral response, indicating that the entire RAB2B-GARIL5 complex regulates the cGAS-STING signalling axis, thus promoting IFN responses against cytosolic DNA (DNA viruses).[10]

RAB2B isoform knockdown affects the morphology of the Golgi complex in mammals, inducing its fragmentation.[11] Even though these RAB family proteins are highly homologous to each other (RAB2A and RAB2B have 85.8% amino acid identity), the knockdown of any of them (from RAB1A to RAB8A) causes Golgi complex to disperse through the cell's cytoplasm. Because of this, the RAB2B-GARIL5 complex stops functioning properly, affecting the IFN response[10] and enhancing the replication of many viruses, as seen previously.

The expression pattern of the human RAB2B gene reveals a transcript in kidney, prostate, lung, thymus, and colon, and a lower expression level in placenta, pancreas and skeletal muscle. Moreover, it is shown that the transcript is over-expressed in colon adenocarcinoma, as well as pancreatic cancer.[12] This observation entails that this protein could have a close relationship with colon tumours.[13]

• Overview of all the structural information available in the PDB for UniProt: Q8WUD1 (Ras-related protein Rab-2B) at the PDBe-KB.