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基于酶的生物硅和生物方解石:再生医学中未来的生物材料。

Enzyme-based biosilica and biocalcite: biomaterials for the future in regenerative medicine.

机构信息

ERC Advanced Investigator Grant Research Group, Institute for Physiological Chemistry, University Medical Center, Johannes Gutenberg University Mainz, Duesbergweg 6, D-55128 Mainz, Germany.

ERC Advanced Investigator Grant Research Group, Institute for Physiological Chemistry, University Medical Center, Johannes Gutenberg University Mainz, Duesbergweg 6, D-55128 Mainz, Germany.

出版信息

Trends Biotechnol. 2014 Sep;32(9):441-7. doi: 10.1016/j.tibtech.2014.05.004. Epub 2014 Jun 4.

Abstract

The oldest animals on Earth, sponges, form both the calcareous and the siliceous matrices of their spicules enzymatically. Until recently, it has been neglected that enzymes play crucial roles during formation of these biominerals. This paradigm shift occurred after the discovery that the enzyme silicatein, which catalyzes the polycondensation of silica, and the enzyme carbonic anhydrase (CA), which catalyzes the formation of bicarbonate (HCO3(-)/CaCO3), produce solid amorphous bioglass or biocalcite. This suggests that in mammals, biosilica and biocalcite can act anabolically during hydroxyapatite (HA) synthesis and bone formation. Biosilica and biocalcite are thus promising candidates for the fabrication of biomaterials for regenerative medicine.

摘要

地球上最古老的动物——海绵,通过酶的作用形成它们的骨针的钙质和硅质基质。直到最近,人们才忽视了酶在这些生物矿物质形成过程中所起的关键作用。这一范式的转变发生在发现了能够催化硅聚合的酶——硅蛋白和催化碳酸氢根(HCO3(-)/CaCO3)形成的酶——碳酸酐酶(CA)之后,这两种酶可以产生固体无定形生物玻璃或生物方解石。这表明,在哺乳动物中,生物硅和生物方解石可以在羟磷灰石(HA)合成和骨形成过程中发挥合成代谢作用。因此,生物硅和生物方解石是再生医学中生物材料制造的有前途的候选材料。

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