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血红蛋白的扩散和红细胞对氧气的捕获动力学。

Hemoglobin diffusion and the dynamics of oxygen capture by red blood cells.

机构信息

Laboratoire Léon Brillouin, CEA, CNRS, Université Paris-Saclay, CEA-Saclay, F-91191, Gif-sur-Yvette, France.

Juelich Centre for Neutron Science, outstation at SNS, Oak Ridge National Laboratory, Oak Ridge, TN, 37831, USA.

出版信息

Sci Rep. 2017 Sep 5;7(1):10448. doi: 10.1038/s41598-017-09146-9.

Abstract

Translational diffusion of macromolecules in cell is generally assumed to be anomalous due high macromolecular crowding of the milieu. Red blood cells are a special case of cells filled quasi exclusively (95% of the dry weight of the cell) with an almost spherical protein: hemoglobin. Hemoglobin diffusion has since a long time been recognized as facilitating the rate of oxygen diffusion through a solution. We address in this paper the question on how hemoglobin diffusion in the red blood cells can help the oxygen capture at the cell level and hence to improve oxygen transport. We report a measurement by neutron spin echo spectroscopy of the diffusion of hemoglobin in solutions with increasing protein concentration. We show that hemoglobin diffusion in solution can be described as Brownian motion up to physiological concentration and that hemoglobin diffusion in the red blood cells and in solutions at similar concentration are the same. Finally, using a simple model and the concentration dependence of the diffusion of the protein reported here, we show that hemoglobin concentration observed in human red blood cells ([Formula: see text]330 g.L ) corresponds to an optimum for oxygen transport for individuals under strong activity.

摘要

大分子在细胞中的平动扩散通常被认为是异常的,这是由于环境中高分子的高度拥挤。红细胞是一种特殊的细胞,几乎完全充满了一种几乎呈球形的蛋白质:血红蛋白。很长一段时间以来,血红蛋白的扩散一直被认为可以促进氧气在溶液中的扩散速度。在本文中,我们探讨了血红蛋白在红细胞中的扩散如何有助于细胞水平的氧气捕获,从而改善氧气输送。我们通过中子自旋回波光谱法报告了血红蛋白在蛋白质浓度不断增加的溶液中的扩散测量结果。我们表明,血红蛋白在溶液中的扩散可以用布朗运动来描述,直到生理浓度,并且血红蛋白在红细胞中的扩散和在相似浓度的溶液中的扩散是相同的。最后,使用一个简单的模型和这里报道的蛋白质扩散的浓度依赖性,我们表明,人类红细胞中观察到的血红蛋白浓度([Formula: see text]330 g.L)对于高强度活动的个体的氧气输送是最佳的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78b2/5585185/c16b08e36d06/41598_2017_9146_Fig1_HTML.jpg

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