Takeuchi Akari, Ohtsuki Chikara, Kamitakahara Masanobu, Ogata Shin-ichi, Miyazaki Toshiki, Tanihara Masao
Graduate School of Materials Science, Nara Institute of Science and Technology, 8916-5, Takayama, Ikoma, Nara 630-0192, Japan.
J Mater Sci Mater Med. 2008 Jan;19(1):387-93. doi: 10.1007/s10856-007-3179-2. Epub 2007 Jul 3.
Deposition of a hydroxyapatite layer with similar structure to bone mineral is an attractive approach to the fabrication of bioactive coating layers to achieve direct bonding to living bone. To get successful coating of a hydroxyapatite layer on an organic polymer using a biomimetic solution, it is essential to find organic substrates that can effectively induce heterogeneous nucleation of hydroxyapatite after exposure to the body environment. Our previous study showed that sericin, a type of silk protein, has the ability to induce hydroxyapatite nucleation in a biomimetic solution when the sericin has a beta sheet structure. To confirm the effectiveness of the beta sheet structure in hydroxyapatite nucleation, we focused on investigating hydroxyapatite deposition on a synthetic polypeptide with a beta sheet structure in a biomimetic solution. The beta sheet forming polypeptides with and without carboxyl groups, poly(FE)(3)FG, poly(FQ)(3)FG, poly(LE)(3)LG and poly(LQ)(3)LG, were synthesized in this study. All the polypeptides had mainly beta sheet structure. After soaking the polypeptide films in 1.5SBF, which has 1.5 times the inorganic ion concentrations of human blood plasma, hydroxyapatite formed on the surfaces of the polypeptides with carboxyl groups, poly(FE)(3)FG and poly(LE)(3)LG, within 2 days, but not on those without carboxyl groups, poly(FQ)(3)FG and poly(LQ)(3)LG. We confirmed that the beta sheet structure was effective for hydroxyapatite nucleation even in the synthetic polypeptide. This finding is useful for the future design of organic polymers that can effectively induce nucleation of hydroxyapatite.
沉积具有与骨矿物质相似结构的羟基磷灰石层是制备生物活性涂层以实现与活骨直接结合的一种有吸引力的方法。为了使用仿生溶液在有机聚合物上成功涂覆羟基磷灰石层,找到在暴露于身体环境后能够有效诱导羟基磷灰石异质成核的有机底物至关重要。我们之前的研究表明,丝胶蛋白(一种丝蛋白)在具有β折叠结构时,有能力在仿生溶液中诱导羟基磷灰石成核。为了证实β折叠结构在羟基磷灰石成核中的有效性,我们专注于研究在仿生溶液中羟基磷灰石在具有β折叠结构的合成多肽上的沉积。本研究合成了具有和不具有羧基的形成β折叠的多肽,聚(FE)(3)FG、聚(FQ)(3)FG、聚(LE)(3)LG和聚(LQ)(3)LG。所有多肽主要具有β折叠结构。将多肽膜浸泡在1.5SBF(其无机离子浓度是人血浆的1.5倍)中后,在2天内,具有羧基的多肽聚(FE)(3)FG和聚(LE)(3)LG表面形成了羟基磷灰石,而没有羧基的多肽聚(FQ)(3)FG和聚(LQ)(3)LG表面则没有形成。我们证实,即使在合成多肽中,β折叠结构对羟基磷灰石成核也是有效的。这一发现对于未来能够有效诱导羟基磷灰石成核的有机聚合物的设计很有用。