Selective binding of C-6 OH sulfated hyaluronic acid to the angiogenic isoform of VEGF(165)

• Published in: Biomaterials Vol. 77; pp. 130 - 138
• Main Authors: Lim, Dong-Kwon, Wylie, Ryan G, Langer, Robert, Kohane, Daniel S
• Format: Journal Article
• Language: English
• Published: Netherlands 01.01.2016
• Subjects: Amino Acid Sequence; Angiogenesis Inhibitors - chemical synthesis; Angiogenesis Inhibitors - metabolism; Angiogenesis Inhibitors - pharmacology; Bevacizumab - metabolism; Carbohydrate Conformation; Chondroitin Sulfates - metabolism; Drug Evaluation, Preclinical; Human Umbilical Vein Endothelial Cells; Humans; Hyaluronic Acid - analogs & derivatives; Hyaluronic Acid - chemical synthesis; Hyaluronic Acid - metabolism; Hyaluronic Acid - pharmacology; Kinetics; Molecular Sequence Data; Molecular Weight; Neovascularization, Physiologic - drug effects; Protein Binding; Protein Structure, Tertiary; Recombinant Proteins - metabolism; Substrate Specificity; Vascular Endothelial Growth Factor A - metabolism; Sulfated sodium hyaluronate; Angiogenesis; Vascular endothelial growth factor 165; VEGF(165a); VEGF(165b); Selective binding property
• ISSN: 1878-5905
• DOI: 10.1016/j.biomaterials.2015.10.074

Vascular endothelial growth factor 165 (VEGF165) is an important extracellular protein involved in pathological angiogenesis in diseases such as cancer, wet age-related macular degeneration (wet-AMD) and retinitis pigmentosa. VEGF165 exists in two different isoforms: the angiogenic VEGF165a, and the anti-angiogenic VEGF165b. In some angiogenic diseases the proportion of VEGF165b may be equal to or higher than that of VEGF165a. Therefore, developing therapeutics that inhibit VEGF165a and not VEGF165b may result in greater anti-angiogenic activity and therapeutic benefit. To this end, we report the selective binding properties of sulfated hyaluronic acid (s-HA). Selective biopolymers offer several advantages over antibodies or aptamers including cost effective and simple synthesis, and the ability to make nanoparticles or hydrogels for drug delivery applications or VEGF165a sequestration. Limiting sulfation to the C-6 hydroxyl (C-6 OH) in the N-acetyl-glucosamine repeat unit of hyaluronic acid (HA) resulted in a polymer with strong affinity for VEGF165a but not VEGF165b. Increased sulfation beyond the C-6 OH (i.e. greater than 1 sulfate group per HA repeat unit) resulted in s-HA polymers that bound both VEGF165a and VEGF165b. The C-6 OH sulfated HA (Mw 150 kDa) showed strong binding properties to VEGF165a with a fast association rate constant (Ka; 2.8 × 10(6) M(-1) s(-1)), slow dissociation rate constant (Kd; 2.8 × 10(-3) s(-1)) and strong equilibrium binding constant (KD; ∼1.0 nM)), which is comparable to the non-selective VEGF165 binding properties of the commercialized therapeutic anti-VEGF antibody (Avastin(®)). The C-6 OH sulfated HA also inhibited human umbilical vein endothelial cell (HUVEC) survival and proliferation and human dermal microvascular endothelial cell (HMVEC) tube formation. These results demonstrate that the semi-synthetic natural polymer, C-6 OH sulfated HA, may be a promising biomaterial for the treatment of angiogenesis-related disease.