# Structural basis of lipid-linked galactan export by the mycobacterial ABC transporter Wzm-Wzt

## TL;DR

This study reveals how mycobacteria transport a key cell wall component using a transporter called Wzm-Wzt, based on detailed structural and functional analysis.

## Contribution

The paper provides the first structural and mechanistic insights into the Wzm-Wzt transporter's role in lipid-linked galactan export.

## Key findings

- Cryo-EM structures of Wzm-Wzt show different conformations during the transport cycle.
- The cytosolic gate helix is essential for polysaccharide transport.
- The hydrophobic polyprenyl-moiety is translocated before the galactan-polysaccharide.

## Abstract

Mycobacteria, including Mycobacterium tuberculosis, possess a unique cell envelope containing arabinogalactan, a heteropolysaccharide critical for cell wall integrity and target of several tuberculosis drugs. The cytosolic precursor of arabinogalactan, lipid-linked galactan (LLG), is translocated across the plasma membrane by the essential ABC transporter Wzm-Wzt through a molecular mechanism that is poorly understood. Here, we present a series of cryo-EM structures of Wzm-Wzt from Mycobacterium abscessus, representing different conformations of the transport cycle. Conserved residues lining the proposed LLG translocation pathway were investigated by three orthologous functional assays, revealing that the cytosolic gate helix (GH) plays a key functional role in polysaccharide transport. Our data suggests that the hydrophobic polyprenyl-moiety is translocated first, followed by the galactan-polysaccharide, which requires Wzm-Wzt to open a continuous channel through which the sugar chain is ratcheted at the expense of ATP hydrolysis. Our results provide a rational basis for the development of drugs that inhibit mycobacterial cell wall biosynthesis.

Mycobacteria require a conserved ABC transporter to export lipid-linked galactan for cell wall biosynthesis. Here, the authors determined multiple cryo-EM structures of this transporter in complex with a substrate analogue, thereby shedding light on the transport mechanism.