Faculty of Mathematics and Natural Sciences, Institute of Biochemistry, University of Cologne, Cologne, Germany.
Division of Infection Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden; Colzyx AB, Lund, Sweden.
J Biol Chem. 2021 Dec;297(6):101169. doi: 10.1016/j.jbc.2021.101169. Epub 2021 Sep 4.
Collagens play important roles in development and homeostasis in most higher organisms. In order to function, collagens require the specific chaperone HSP47 for proper folding and secretion. HSP47 is known to bind to the collagen triple helix, but the exact positions and numbers of binding sites are not clear. Here, we employed a collagen II peptide library to characterize high-affinity binding sites for HSP47. We show that many previously predicted binding sites have very low affinities due to the presence of a negatively charged amino acid in the binding motif. In contrast, large hydrophobic amino acids such as phenylalanine at certain positions in the collagen sequence increase binding strength. For further characterization, we determined two crystal structures of HSP47 bound to peptides containing phenylalanine or leucine. These structures deviate significantly from previously published ones in which different collagen sequences were used. They reveal local conformational rearrangements of HSP47 at the binding site to accommodate the large hydrophobic side chain from the middle strand of the collagen triple helix and, most surprisingly, possess an altered binding stoichiometry in the form of a 1:1 complex. This altered stoichiometry is explained by steric collisions with the second HSP47 molecule present in all structures determined thus far caused by the newly introduced large hydrophobic residue placed on the trailing strand. This exemplifies the importance of considering all three sites of homotrimeric collagen as independent interaction surfaces and may provide insight into the formation of higher oligomeric complexes at promiscuous collagen-binding sites.
胶原蛋白在大多数高等生物的发育和体内平衡中发挥着重要作用。为了发挥功能,胶原蛋白需要 HSP47 这种特殊的伴侣蛋白来进行正确的折叠和分泌。已知 HSP47 可以与胶原蛋白三螺旋结合,但确切的结合位点和数量尚不清楚。在这里,我们利用胶原蛋白 II 肽文库来鉴定 HSP47 的高亲和力结合位点。我们表明,由于结合基序中存在带负电荷的氨基酸,许多先前预测的结合位点的亲和力非常低。相比之下,胶原蛋白序列中某些位置的大疏水性氨基酸,如苯丙氨酸,会增加结合强度。为了进一步进行表征,我们确定了 HSP47 与含有苯丙氨酸或亮氨酸的肽结合的两个晶体结构。这些结构与之前使用不同胶原蛋白序列的结构有很大的不同。它们揭示了 HSP47 在结合位点处的局部构象重排,以适应胶原蛋白三螺旋中间链的大疏水性侧链,最令人惊讶的是,以 1:1 复合物的形式具有改变的结合计量。这种改变的计量比可以通过与迄今为止所有确定结构中存在的第二个 HSP47 分子发生空间位阻来解释,这是由于在尾随链上引入了新的大疏水性残基。这说明了将同源三聚体胶原蛋白的所有三个位点视为独立相互作用表面的重要性,并可能为在混杂的胶原蛋白结合位点形成更高的寡聚复合物提供了一些见解。