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胶原蛋白原纤维分子间间距随异丙醇的变化:一种组织硬度的机制

Collagen Fibril Intermolecular Spacing Changes with 2-Propanol: A Mechanism for Tissue Stiffness.

作者信息

Wells Hannah C, Sizeland Katie H, Kelly Susyn J R, Kirby Nigel, Hawley Adrian, Mudie Stephen, Haverkamp Richard G

机构信息

School of Engineering and Advanced Technology, Massey University, Private Bag 11222, Palmerston North 4442, New Zealand.

Australian Synchrotron, 800 Blackburn Road, Clayton, Melbourne, Victoria 3168, Australia.

出版信息

ACS Biomater Sci Eng. 2017 Oct 9;3(10):2524-2532. doi: 10.1021/acsbiomaterials.7b00418. Epub 2017 Sep 13.

Abstract

Materials composed primarily of collagen are important as surgical scaffolds and other medical devices and require flexibility. However, the factors that control the suppleness and flexibility of these materials are not well understood. Acellular dermal matrix materials in aqueous mixtures of 2-propanol were studied. Synchrotron-based small-angle X-ray scattering was used to characterize the collagen structure and structural arrangement. Stiffness was measured by bend tests. Bend modulus increased logarithmically with 2-propanol concentration from 0.5 kPa in water to 103 kPa in pure 2-propanol. The intermolecular spacing between tropocollagen molecules decreased from 15.3 to 11.4 Å with increasing 2-propanol concentration while fibril diameter decreased from 57.2 to 37.2 nm. D-spacing initially increased from 63.6 to 64.2 nm at 50% 2-propanol then decreased to 60.3 nm in pure 2-propanol. The decrease in intermolecular spacing and fibril diameter are due to removal of water and the collapse of the hydrogen bond structure between tropocollagen molecules causing closer packing of the molecules within a fibril. We speculate this tighter molecular packing may restrict the sliding of collagen within fibrils, and similar disruption of the extended hydration layer between fibrils may lead to restriction of sliding between fibrils. This mechanism for tissue stiffness may be more general.

摘要

主要由胶原蛋白组成的材料作为手术支架和其他医疗设备很重要,并且需要柔韧性。然而,控制这些材料柔韧性和弹性的因素尚未得到充分理解。对2-丙醇水性混合物中的脱细胞真皮基质材料进行了研究。使用基于同步加速器的小角X射线散射来表征胶原蛋白的结构和结构排列。通过弯曲试验测量刚度。弯曲模量随着2-丙醇浓度从水中的0.5 kPa对数增加到纯2-丙醇中的103 kPa。随着2-丙醇浓度的增加,原胶原蛋白分子之间的分子间距从15.3 Å减小到11.4 Å,而原纤维直径从57.2 nm减小到37.2 nm。在50%的2-丙醇中,D间距最初从63.6 nm增加到64.2 nm,然后在纯2-丙醇中减小到60.3 nm。分子间距和原纤维直径的减小是由于水的去除以及原胶原蛋白分子之间氢键结构的坍塌,导致分子在原纤维内更紧密地堆积。我们推测这种更紧密的分子堆积可能会限制胶原蛋白在原纤维内的滑动,并且原纤维之间延伸的水化层的类似破坏可能会导致原纤维之间滑动的限制。这种组织刚度机制可能更具普遍性。

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