首页> 美国卫生研究院文献>eLife >Protein sequences bound to mineral surfaces persist into deep time
【2h】

Protein sequences bound to mineral surfaces persist into deep time

机译:结合到矿物表面的蛋白质序列持续很长时间

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Proteins persist longer in the fossil record than DNA, but the longevity, survival mechanisms and substrates remain contested. Here, we demonstrate the role of mineral binding in preserving the protein sequence in ostrich (Struthionidae) eggshell, including from the palaeontological sites of Laetoli (3.8 Ma) and Olduvai Gorge (1.3 Ma) in Tanzania. By tracking protein diagenesis back in time we find consistent patterns of preservation, demonstrating authenticity of the surviving sequences. Molecular dynamics simulations of struthiocalcin-1 and -2, the dominant proteins within the eggshell, reveal that distinct domains bind to the mineral surface. It is the domain with the strongest calculated binding energy to the calcite surface that is selectively preserved. Thermal age calculations demonstrate that the Laetoli and Olduvai peptides are 50 times older than any previously authenticated sequence (equivalent to ~16 Ma at a constant 10°C).>DOI:
机译:化石记录中的蛋白质比DNA保留的时间更长,但是寿命,存活机制和底物仍然存在争议。在这里,我们证明了矿物结合在保留鸵鸟(Struthionidae)蛋壳中蛋白质序列中的作用,包括来自坦桑尼亚的Laetoli(3.8 Ma)和Olduvai Gorge(1.3 Ma)的古生物学遗址。通过及时追溯蛋白质的成岩作用,我们发现一致的保存方式,证明了存活序列的真实性。蛋壳中的主要蛋白质struthiocalcin-1和-2的分子动力学模拟显示,不同的结构域与矿物质表面结合。选择性保留的是计算到方解石表面结合能最强的区域。热年龄的计算表明,Laetoli和Olduvai肽的年龄是以前鉴定的任何序列的50倍(在恒定10°C时相当于〜16 Ma)。> DOI:

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号