Project B02

Principal Investigator

Prof. Dr. Thomas Krey & Dr. Gabrielle Vieyres

Universität zu Lübeck

B2

PhD candidate

Niklas Ebersberger


B2

Project Summary

Structural and functional characterization of the scavenger receptor B1 – a cellular receptor for Hepatitis C virus (HCV)

Scavenger receptor class B type 1 (SR-B1), a member of the CD36 superfamily, is a transmembrane protein comprising an N- and C-terminal transmembrane region framing a large ectodomain1. SR-B1 is a lipoprotein receptor and interacts e.g., with high-density lipoproteins (HDL) and promotes the uptake of cholesterol esters to the liver and steroidogenic tissues by oligomerization in the membrane and formation of a channel2. The multifunctional glycoprotein also acts as the initial attachment receptor for the hepatitis C virus (HCV), either via 1) a direct interaction between the hypervariable region 1 of the major HCV glycoprotein E2 and SR-B1, or 2) an effect of SR-B1 activity on high-density lipoproteins (HDL) associated to infectious HCV particles3. Our goal is to gain insights into the role of SR-B1 in HCV entry using structural virology approaches combined with fluorescent imaging.

B2

References

  1. Acton, S. et al. Identification of scavenger receptor SR-BI as a high density lipoprotein receptor. Science 271, 518–520 (1996).
  2. Marques, P. E. et al. Multimerization and Retention of the Scavenger Receptor SR-B1 in the Plasma Membrane. Dev. Cell 50, 283-295.e5 (2019).
  3. Lindenbach, B. D. & Rice, C. M. The ins and outs of hepatitis C virus entry and assembly. Nat. Rev. Microbiol.11, 688–700 (2013).