首页> 外文期刊>Journal of proteome research >Human Bone Proteomes before and after Decomposition: Investigating the Effects of Biological Variation and Taphonomic Alteration on Bone Protein Profiles and the Implications for Forensic Proteomics
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Human Bone Proteomes before and after Decomposition: Investigating the Effects of Biological Variation and Taphonomic Alteration on Bone Protein Profiles and the Implications for Forensic Proteomics

机译:分解前后的人骨蛋白质:研究生物学变化和术语的影响,对骨蛋白质谱的影响及法医蛋白质组学的影响

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摘要

Bone proteomic studies using animal proxies and skeletonized human remains have delivered encouraging results in the search for potential biomarkers for precise and accurate postmortem interval (PMI) and the age-at-death (AAD) estimation in medico-legal investigations. The development of forensic proteomics for PMI and AAD estimation is in critical need of research on human remains throughout decomposition, as currently the effects of both inter-individual biological differences and taphonomic alteration on the survival of human bone protein profiles are unclear. This study investigated the human bone proteome in four human body donors studied throughout decomposition outdoors. The effects of ageing phenomena (in vivo and post-mortem) and intrinsic and extrinsic variables on the variety and abundancy of the bone proteome were assessed. Results indicate that taphonomic and biological variables play a significant role in the survival of proteins in bone. Our findings suggest that inter-individual and inter-skeletal differences in bone mineral density (BMD) are important variables affecting the survival of proteins. Specific proteins survive better within the mineral matrix due to their mineral-binding properties. The mineral matrix likely also protects these proteins by restricting the movement of decomposer microbes. New potential biomarkers for PMI estimation and AAD estimation were identified. Future development of forensic bone proteomics should include standard measurement of BMD and target a combination of different biomarkers.
机译:使用动物替代物和骨骼化人类遗骸进行的骨蛋白质组学研究在寻找法医学调查中精确和准确的死亡时间间隔(PMI)和死亡年龄(AAD)估计的潜在生物标记物方面取得了令人鼓舞的结果。用于PMI和AAD估计的法医蛋白质组学的发展是整个分解过程中人类遗骸研究的关键需求,因为目前尚不清楚个体间生物学差异和直系组学改变对人类骨蛋白图谱存活的影响。本研究调查了四名人体供体在户外分解过程中的人体骨蛋白质组。评估了衰老现象(体内和死后)以及内在和外在变量对骨蛋白质组多样性和丰度的影响。结果表明,埋藏组学和生物学变量对骨中蛋白质的存活起着重要作用。我们的研究结果表明,个体间和骨骼间骨密度(BMD)的差异是影响蛋白质存活的重要变量。由于矿物质结合特性,特定蛋白质在矿物质基质中存活得更好。矿物质基质也可能通过限制分解微生物的移动来保护这些蛋白质。确定了用于PMI估计和AAD估计的新的潜在生物标志物。法医骨蛋白质组学的未来发展应包括BMD的标准测量和针对不同生物标记物的组合。

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