Center for Advanced Jet Engineering Technologies (CaJET), Key Laboratory of High-efficiency and Clean Mechanical Manufacture (Ministry of Education), Department of Mechanical Engineering , Shandong University , Jingshi Road 17923 , Jinan 250061 , China.
Department of Chemical and Materials Engineering , University of Alberta , Edmonton , Alberta T6G 1H9 , Canada.
Biomacromolecules. 2019 Feb 11;20(2):1056-1067. doi: 10.1021/acs.biomac.8b01678. Epub 2019 Jan 16.
Probing the adsorption and lubrication behavior of lubricin, also known as proteoglycan 4 (PRG4), is important for understanding the ultralow friction of cartilage lubrication. Most previous research has focused on native lubricin either purified from synovial fluid or articular cartilage explant culture media. In this work, the adsorption behavior and lubrication mechanism of full-length recombinant human PRG4 (rhPRG4) on mica as well as the effect of adding hyaluronic acid (HA, a polysaccharide) were systematically investigated using a surface forces apparatus (SFA) technique. A low friction coefficient (μ ∼ 0.04) was measured when multilayer rhPRG4 (∼31 nm) was confined in between mica surfaces, even when the load increased to ∼1.2 MPa. Intriguingly, a previously unreported ultralow friction coefficient (μ < 0.005) was observed at a low sliding velocity ( v = 0.14 μm/s) with the applied load P reaching ∼3.6 MPa when a diluted rhPRG4 solution (∼90 μg/mL) was used. The distinct friction behavior is likely due to the smooth and more close-packed lubricin coating, as made evident by the atomic force microscope imaging. Adding HA onto multilayer rhPRG4-coated mica increased the friction coefficient μ to ∼0.1; however, the load bearing property increased, indicating potential synergistic effect between rhPRG4 and HA, which was further demonstrated by the weak adhesion observed when separating rhPRG4-coated mica and HA-coated aminopropyltriethoxysilane-mica (APTES-mica). Alternatively, adding premixed rhPRG4-HA on mica had a friction coefficient (μ ∼ 0.1) close to that of injecting concentrated rhPRG4 (∼450 μg/mL) with lower load sustainability. Our results provide fundamental insights into the adsorption and lubrication behavior of lubricin and its interaction with HA, with useful implications for the underlying mechanism of ultralow friction provided by synovial fluid.
探究黏蛋白(也称为蛋白聚糖 4,PRG4)的吸附和润滑行为对于理解软骨润滑的超低摩擦非常重要。之前的大多数研究都集中在从滑液或关节软骨组织培养物中纯化的天然黏蛋白。在这项工作中,使用原子力显微镜(AFM)技术系统地研究了全长重组人 PRG4(rhPRG4)在云母上的吸附行为和润滑机制,以及添加透明质酸(HA,一种多糖)的影响。当多层 rhPRG4(约 31nm)被限制在云母表面之间时,测量到低摩擦系数(μ∼0.04),即使在负载增加到约 1.2MPa 时也是如此。有趣的是,当使用稀释的 rhPRG4 溶液(约 90μg/mL)时,在低滑动速度(v=0.14μm/s)和施加的负载 P 达到约 3.6MPa 时,观察到以前未报道的超低摩擦系数(μ<0.005)。这种明显的摩擦行为可能是由于润滑蛋白的光滑和更紧密堆积的涂层,这从原子力显微镜成像中可以明显看出。在多层 rhPRG4 涂层的云母上添加 HA 会将摩擦系数μ增加到约 0.1;然而,承载能力增加,表明 rhPRG4 和 HA 之间存在潜在的协同作用,这进一步通过分离 rhPRG4 涂层云母和 HA 涂层氨丙基三乙氧基硅烷云母(APTES-mica)时观察到的弱粘附得到证明。或者,在云母上添加预混合的 rhPRG4-HA 的摩擦系数(μ∼0.1)与注射浓缩 rhPRG4(∼450μg/mL)的摩擦系数相近,但负载可持续性较低。我们的研究结果为黏蛋白的吸附和润滑行为及其与 HA 的相互作用提供了基本的认识,对滑液提供超低摩擦的潜在机制具有重要意义。