Aguirre K M, McCormick R J, Schwarzbauer J E
Department of Molecular Biology, Princeton University, New Jersey 08544-1014.
J Biol Chem. 1994 Nov 11;269(45):27863-8.
The formation of a fibrillar fibronectin (FN) extracellular matrix requires self-association of FN dimers. In this report, we show that the major sites for self-association are the amino-terminal repeats I1-5 and the first type III repeats. Recombinant FNs and fragments were generated by baculovirus expression of cysteine-rich domains and by bacterial expression of type III repeats as fusion proteins with maltose binding protein. When recombinant polypeptides were immobilized on microtiter wells, FN bound to 70-kDa amino-terminal fragment and to fusion proteins containing repeats III1-2 and III1-6 but not to other type III repeats. Similar results were obtained with a gel overlay assay. Binding was concentration-dependent and saturable. The amino-terminal binding site for III1-2 was further localized to repeats I1-5. Therefore, at least two different sites for FN-FN interaction reside near the amino terminus of the molecule. A model for the regulation of FN matrix assembly is proposed based on intramolecular interactions between these amino-terminal sites.
纤维状纤连蛋白(FN)细胞外基质的形成需要FN二聚体的自我缔合。在本报告中,我们表明自我缔合的主要位点是氨基末端重复序列I1 - 5和第一个III型重复序列。通过杆状病毒表达富含半胱氨酸的结构域以及通过细菌表达作为与麦芽糖结合蛋白的融合蛋白的III型重复序列来产生重组FN和片段。当重组多肽固定在微量滴定板孔上时,FN与70 kDa的氨基末端片段以及含有重复序列III1 - 2和III1 - 6的融合蛋白结合,但不与其他III型重复序列结合。凝胶覆盖试验也得到了类似的结果。结合是浓度依赖性的且可饱和的。III1 - 2的氨基末端结合位点进一步定位于重复序列I1 - 5。因此,至少两个不同的FN - FN相互作用位点位于分子的氨基末端附近。基于这些氨基末端位点之间的分子内相互作用,提出了一个FN基质组装调控模型。