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Structure of the trypanosome transferrin receptor reveals mechanisms of ligand recognition and immune evasion


To maintain prolonged infection of mammals, African trypanosomes have evolved remarkable surface coats and a system of antigenic variation1. Within these coats are receptors for macromolecular nutrients such as transferrin2,3. These must be accessible to their ligands but must not confer susceptibility to immunoglobulin-mediated attack. Trypanosomes have a wide host range and their receptors must also bind ligands from diverse species. To understand how these requirements are achieved, in the context of transferrin uptake, we determined the structure of a Trypanosoma brucei transferrin receptor in complex with human transferrin, showing how this heterodimeric receptor presents a large asymmetric ligand-binding platform. The trypanosome genome contains a family of around 14 transferrin receptors4, which has been proposed to allow binding to transferrin from different mammalian hosts5,6. However, we find that a single receptor can bind transferrin from a broad range of mammals, indicating that receptor variation is unlikely to be necessary for promiscuity of host infection. In contrast, polymorphic sites and N-linked glycans are preferentially found in exposed positions on the receptor surface, not contacting transferrin, suggesting that transferrin receptor diversification is driven by a need for antigenic variation in the receptor to prolong survival in a host.

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Fig. 1: The structure of the trypanosome transferrin receptor.
Fig. 2: The role of the trypanosome transferrin receptor in pH-dependent transferrin binding and iron release.
Fig. 3: Binding of the transferrin receptor to transferrin from different mammalian species.
Fig. 4: Glycans and sequence diversity concentrate around the membrane-distal head of the transferrin receptor.

Data availability

Crystallographic data, including molecular models and reflection data, are available in the Protein Data Bank with accession codes 6SOY and 6SOZ. All other data and constructs are available on request from the corresponding authors.


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This work was supported by a research grant from the Medical Research Council (grant no. MR/R001138/1). C.E.T. holds a BBSRC iCASE studentship. M.K.H. is a Wellcome Investigator. The authors are grateful for the assistance of E. Lowe and the beamline scientists of beamline I03 at Diamond Light Source with crystallographic data collection. They also thank G. Grime at the Surrey Ion Beam Centre for assistance with μPIXE data collection, which was funded through EPSRC grant no. NS/A000059/1 to the UK National Ion Beam Centre.

Author information




C.E.T. performed protein production, crystallization and surface plasmon resonance analysis. C.E.T. and M.K.H. determined the crystal structure. C.E.T., O.J.S.M. and M.C. conducted growth and expression analyses. P.G.W. and E.F.G. performed and analysed μPIXE experiments. A.L.G., S.R., T.J.V. and R.M. participated in design and experimental coordination. C.E.T., M.C. and M.K.H. devised the study and wrote the manuscript.

Corresponding authors

Correspondence to Mark Carrington or Matthew K. Higgins.

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Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Extended data

Extended Data Fig. 1 Phylogenic analysis of transferrin receptors.

a. Evolutionary trees showing the relatedness of different transferrin receptor variants within the blood stream expression sites of the Lister 427 strain. The BES1 and BES17 receptors are highlighted in red. b. Comparison of the BES17 ESAG6 and ESAG7 proteins. The black box indicates the signal sequence and the dashed black box indicates the GPI-anchor addition site. Blue cylinders represent the helical regions of the structure. Red stars mark residues which make direct contacts with human transferrin. Orange highlighting of the text indicates residues which differ between ESAG6 and ESAG7.

Extended Data Fig. 2 Data collection and refinement statistics.

Table of data collection and refinement statistics for crystal structures.

Extended Data Fig. 3 Comparison of the transferrin receptor with VSGs and the haptoglobin-haemoglobin receptor.

a. Structural alignment of the transferrin receptor with known VSG structures, 1VSG (orange), 2VSG (yellow) and 5LY9 (pink) and the Trypanosoma brucei haptoglobin–haemoglobin receptor (TbHpHbR, red). b. Sequence alignment of the two subunits of the transferrin receptor with the three VSGs. Orange highlighting indicates divergent residues.

Extended Data Fig. 4 Sequence alignment of mammalian transferrin variants analysed in this study.

a. Phylogenic tree of placental mammals adapted from ref. 36. b. Sequence alignment of selected transferrin variants. Variable residues are highlighted in orange and residues which directly contact the BES17 transferrin receptor are indicated by red stars. Green circles identify residues which contact the human transferrin receptor.

Extended Data Fig. 5 Table of interactions.

Table of interactions between the trypanosome transferrin receptor and transferrin.

Extended Data Fig. 6 Surface plasmon resonance analysis.

Measurement of kinetic binding parameters for transferrin receptor variants to transferrins. BES1mut has a G139R mutation in ESAG6 and S246Y I229V and C223R in ESAG7. ESAG6 is e6 and ESAG7 is e7 in the table.

Extended Data Fig. 7 Elemental analysis by mPIXE to determine the number of Fe ions per transferrin or transferrin:TfR complex at different pH values.

Plots of counts per channel for emission induced by different photon energies, annotated with the element responsible for emission. Comparison of the quantities of Fe and S, together with knowledge of the protein sequences, and the numbers of S atoms, allowed determination of the number of Fe ions per transferrin or transferrin:TfR complex. Data shown is representative of three technical replicates.

Extended Data Fig. 8 Comparison of the sequences of BES17 and BES1 transferrin receptors.

Sequence alignments of ESAG6 subunits and ESAG7 subunits. Numbering is according to the BES17 sequence, which matches that of the crystal structure. Residues highlighted in orange vary between the BES1 and BES17 variants. Residues indicated by a red star directly contact human transferrin in the BES17 receptor. Residues indicated by a blue triangle are those mutated in the BES1mut mutant. Residues boxed with a continuous line represent the putative signal peptides while those boxed with a discontinuous line represent the GPI-anchor addition sequence.

Extended Data Fig. 9 SPR analysis of transferrin receptor variants and mutants.

a. Analysis of the binding of chimeric receptors formed between the ESAG6 and ESA7 subunits of the BES1 and BES17 transferrin receptor variants to human transferrin by surface plasmon resonance. b. Analysis of the binding to human and rat transferrin of mutants of the BES1 transferrin receptor. Each concentration series was performed once.

Extended Data Fig. 10 Analysis of transferrin receptor expression during growth in sera from different mammals.

a. Sequences of ESAG7 from different transferrin receptor variants within the blood stream expression sites of the Lister 427 strain, showing nucleotide sequences equivalent to 778 to 837 in the BES1 sequence. Below this are shown the predominant sequences found in Trypanosoma brucei cells grown in serum exclusively containing cow, horse, rabbit and pig transferrin for 309 hours. The red lettering and red star indicate a sequence difference at position 798 in which a T is unique to the BES1 receptor. b. Sequencing chromatograms of the expressed transferrin receptor variants in cells, showing nucleotides equivalent to 791 to 805 in the BES1 sequence. The star marks residue 798, which is T in BES1 and C in the other receptors in the Lister 427 strain. The top chromatogram shows that Trypanosoma brucei grown in fetal calf serum (cow) for 72 hours predominantly express BES1. These cells were transferred into media containing serum from cow, pig, horse or rabbit and were grown for a further 119 hours (the 191h time point) and 309 hours (the 381h time point) and the chromatograms show the transferrin receptor sequences expressed at these times remains predominantly BES1, with lower levels of other receptors in all four sera. A similar outcome was seen for ESAG6 sequences (not shown).

Supplementary information

Reporting Summary

Supplementary Table 1

Sequences used for sequence entropy calculations.

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Trevor, C.E., Gonzalez-Munoz, A.L., Macleod, O.J.S. et al. Structure of the trypanosome transferrin receptor reveals mechanisms of ligand recognition and immune evasion. Nat Microbiol 4, 2074–2081 (2019).

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