Structural basis for chemokine recognition and activation of a viral G protein–coupled receptor

Author:

Burg John S.123,Ingram Jessica R.4,Venkatakrishnan A. J.356,Jude Kevin M.123,Dukkipati Abhiram123,Feinberg Evan N.356,Angelini Alessandro7,Waghray Deepa123,Dror Ron O.356,Ploegh Hidde L.4,Garcia K. Christopher123

Affiliation:

1. Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.

2. Department of Structural Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.

3. Department of Molecular and Cellular Physiology, Stanford University School of Medicine, Stanford, CA 94305, USA.

4. Whitehead Institute for Biomedical Research, 9 Cambridge Center, Cambridge, MA 02142, USA.

5. Department of Computer Science, Stanford University, Stanford, CA 94305, USA.

6. Institute for Computational and Mathematical Engineering, Stanford University, Stanford, CA 94305, USA.

7. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA 02139, USA.

Abstract

Molecular “go” signals reveal their secrets Chemokines are proteins that direct how cells move within the body. For instance, chemokines help immune cells locate invading pathogens and ensure that cells position themselves correctly within a developing organ. Cells detect chemokines through G protein–coupled receptors on their surface; however, the molecular details of how these proteins interact remain unclear (see the Perspective by Standfuss). Qin et al. solved the crystal structure of the chemokine receptor CXCR4 bound to the viral chemokine vMIP-II. Burg et al. solved the crystal structure of a viral chemokine receptor bound to the chemokine domain of CX3CL1. Given the role of chemokines in a number of diseases, these results may help in future drug design. Science , this issue p. 1117 , p. 1113 ; see also p. 1071

Funder

NIH

Howard Hughes Medical Institute

Cancer Research Institute

Swiss National Science Foundation

Keck Foundation Medical Scholars Program

Terman Faculty Fellowship

Ludwig Foundation for Cancer Research

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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