Department of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati, College of Medicine, Cincinnati, Ohio 45267, USA.
Department of Chemical and Biological Engineering, Center for Biotechnology and Interdisciplinary Studies, Rensselaer Polytechnic Institute, Troy, New York 12180, USA.
Exp Biol Med (Maywood). 2021 Feb;246(4):467-482. doi: 10.1177/1535370220966296. Epub 2020 Nov 16.
Heparin and heparan sulfate (HS) are highly sulfated polysaccharides covalently bound to cell surface proteins, which directly interact with many extracellular proteins, including the transforming growth factor-β (TGFβ) family ligand antagonist, follistatin 288 (FS288). Follistatin neutralizes the TGFβ ligands, myostatin and activin A, by forming a nearly irreversible non-signaling complex by surrounding the ligand and preventing interaction with TGFβ receptors. The FS288-ligand complex has higher affinity than unbound FS288 for heparin/HS, which accelerates ligand internalization and lysosomal degradation; however, limited information is available for how FS288 interactions with heparin affect ligand binding. Using surface plasmon resonance (SPR) we show that preincubation of FS288 with heparin/HS significantly decreased the association kinetics for both myostatin and activin A with seemingly no effect on the dissociation rate. This observation is dependent on the heparin/HS chain length where small chain lengths less than degree of polymerization 10 (dp10) did not alter association rates but chain lengths >dp10 decreased association rates. In an attempt to understand the mechanism for this observation, we uncovered that heparin induced dimerization of follistatin. Consistent with our SPR results, we found that dimerization only occurs with heparin molecules >dp10. Small-angle X-ray scattering of the FS288 heparin complex supports that FS288 adopts a dimeric configuration that is similar to the FS288 dimer in the ligand-bound state. These results indicate that heparin mediates dimerization of FS288 in a chain-length-dependent manner that reduces the ligand association rate, but not the dissociation rate or antagonistic activity of FS288.
肝素和硫酸乙酰肝素 (HS) 是通过共价键与细胞表面蛋白结合的高度硫酸化多糖,它们直接与许多细胞外蛋白相互作用,包括转化生长因子-β (TGFβ) 家族配体拮抗剂,卵泡抑素 288 (FS288)。卵泡抑素通过围绕配体并阻止其与 TGFβ 受体相互作用,形成几乎不可逆的非信号复合物,从而中和 TGFβ 配体,如肌肉生长抑制素和激活素 A。FS288-配体复合物与肝素/HS 的亲和力高于未结合的 FS288,这加速了配体的内化和溶酶体降解;然而,关于 FS288 与肝素相互作用如何影响配体结合的信息有限。我们使用表面等离子体共振 (SPR) 表明,FS288 与肝素/HS 预孵育显著降低了肌肉生长抑制素和激活素 A 与 FS288 的结合动力学,而对解离速率似乎没有影响。这种观察结果取决于肝素/HS 的链长,其中短链长度小于聚合度 10 (dp10) 不会改变结合速率,但链长>dp10 会降低结合速率。为了理解这种观察结果的机制,我们发现肝素诱导卵泡抑素二聚化。与我们的 SPR 结果一致,我们发现只有肝素分子>dp10 才会发生二聚化。FS288 肝素复合物的小角 X 射线散射支持 FS288 采用类似于配体结合状态下 FS288 二聚体的二聚体构象。这些结果表明,肝素以链长依赖性方式介导 FS288 的二聚化,从而降低配体结合速率,但不降低 FS288 的解离速率或拮抗活性。