Smith D K, Treutlein H R
Ludwig Institute for Cancer Research, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.
Protein Sci. 1998 Apr;7(4):886-96. doi: 10.1002/pro.5560070406.
Leukemia inhibitory factor (LIF), a member of the gp130 family of helical cytokines, is involved in the hemopoietic and neural systems. The LIF signal transducing complex contains two receptor molecules, the LIF receptor (LIFR) and gp130. The extracellular region of the LIFR is unique in that it includes three membrane-proximal fibronectin type III domains and two cytokine binding domains (CBDs) separated by an immunoglobulin-like domain. Although some mutagenesis data on LIF are available, it is not yet known which regions of LIFR or gp130 bind LIF. Nor is it known whether LIFR contacts gp130 in a manner similar to the growth hormone receptor dimer and, if so, through which of its CBDs. To attempt to elucidate these matters and to investigate the receptor complex, models of the CBDs of LIFR and the CBD of gp130 were constructed. Analyses of the electrostatic isopotential surfaces of the CBD models suggest that gp130 and the membrane-proximal CBD of LIFR hetero-dimerize and bind LIF through contacts similar to those seen in the growth hormone receptor dimer. This work further demonstrates the utility of electrostatic analyses of homology models and suggests a strategy for biochemical investigations of the LIF-receptor complex.
白血病抑制因子(LIF)是螺旋细胞因子gp130家族的成员,参与造血和神经系统。LIF信号转导复合物包含两个受体分子,即LIF受体(LIFR)和gp130。LIFR的细胞外区域独特之处在于它包括三个膜近端III型纤连蛋白结构域和两个由免疫球蛋白样结构域隔开的细胞因子结合结构域(CBD)。尽管已有一些关于LIF的诱变数据,但尚不清楚LIFR或gp130的哪些区域结合LIF。也不清楚LIFR是否以类似于生长激素受体二聚体的方式与gp130接触,如果是这样,是通过其哪个CBD接触。为了试图阐明这些问题并研究受体复合物,构建了LIFR的CBD模型和gp130的CBD模型。对CBD模型的静电等势面分析表明,gp130和LIFR的膜近端CBD异源二聚化,并通过与生长激素受体二聚体中类似的接触结合LIF。这项工作进一步证明了同源模型静电分析的实用性,并提出了一种对LIF受体复合物进行生化研究的策略。