Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Structural and Functional Basis of CXCL12 (stromal cell-derived factor-1 alpha) Binding to Heparin

Journal Article · · Journal of Biological Chemistry

CXCL12 (SDF-1a) and CXCR4 are critical for embryonic development and cellular migration in adults. These proteins are involved in HIV-1 infection, cancer metastasis, and WHIM disease. Sequestration and presentation of CXCL12 to CXCR4 by glycosaminoglycans (GAGs) is proposed to be important for receptor activation. Mutagenesis has identified CXCL12 residues that bind to heparin. However, the molecular details of this interaction have not yet been determined. Here we demonstrate that soluble heparin and heparan sulfate negatively affect CXCL12-mediated in vitro chemotaxis. We also show that a cluster of basic residues in the dimer interface is required for chemotaxis and is a target for inhibition by heparin. We present structural evidence for binding of an unsaturated heparin disaccharide to CXCL12 attained through solution NMR spectroscopy and x-ray crystallography. Increasing concentrations of the disaccharide altered the two-dimensional 1H-15N-HSQC spectra of CXCL12, which identified two clusters of residues. One cluster corresponds to {beta}-strands in the dimer interface. The second includes the amino-terminal loop and the a-helix. In the x-ray structure two unsaturated disaccharides are present. One is in the dimer interface with direct contacts between residues His25, Lys27, and Arg41 of CXCL12 and the heparin disaccharide. The second disaccharide contacts Ala20, Arg21, Asn30, and Lys64. This is the first x-ray structure of a CXC class chemokine in complex with glycosaminoglycans. Based on the observation of two heparin binding sites, we propose a mechanism in which GAGs bind around CXCL12 dimers as they sequester and present CXCL12 to CXCR4.

Research Organization:
Brookhaven National Laboratory (BNL) National Synchrotron Light Source
Sponsoring Organization:
Doe - Office Of Science
DOE Contract Number:
AC02-98CH10886
OSTI ID:
959591
Report Number(s):
BNL--82577-2009-JA
Journal Information:
Journal of Biological Chemistry, Journal Name: Journal of Biological Chemistry Journal Issue: 13 Vol. 282; ISSN JBCHA3; ISSN 0021-9258
Country of Publication:
United States
Language:
English

Similar Records

Heterologous Quaternary Structure of CXCL12 and its Relationship to the CC Chemokine Family
Journal Article · Thu Dec 31 23:00:00 EST 2009 · Proteins: Structure, Functions, and Bioinformatics · OSTI ID:1020113

PI3K{gamma} activation by CXCL12 regulates tumor cell adhesion and invasion
Journal Article · Fri Oct 16 00:00:00 EDT 2009 · Biochemical and Biophysical Research Communications · OSTI ID:22199836

The 5T4 oncofetal glycoprotein does not act as a general organizer of the CXCL12 system in cancer cells
Journal Article · Thu Mar 15 00:00:00 EDT 2018 · Experimental Cell Research · OSTI ID:23082424