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利用荧光肽偶联 Au 纳米颗粒探针检测人膝关节滑液中的 ADAMTS-4 活性。

Detection of ADAMTS-4 activity using a fluorogenic peptide-conjugated Au nanoparticle probe in human knee synovial fluid.

机构信息

Institute of Sports Medicine, Peking University Third Hospital, Haidian District, Beijing, P R China.

出版信息

ACS Appl Mater Interfaces. 2013 Jul 10;5(13):6089-96. doi: 10.1021/am400854z. Epub 2013 Jun 24.

Abstract

A disintegrin and metalloproteinase with thrombospondin motif-4 (ADAMTS-4) plays a pivotal role in degrading aggrecan, which is an early event in cartilage degrading joint diseases such as osteoarthritis (OA). Detection of ADAMTS-4 activity could provide useful clinical information for early diagnosis of such diseases and disease-modifying therapy. Therefore, we developed a ADAMTS-4 detective fluorescent turn-on AuNP probe (ADAMTS-4-D-Au probe) by conjugating gold nanoparticles with a FITC-modified ADAMTS-4-specific peptide (DVQEFRGVTAVIR). When the ADAMTS-4-D-Au probe was incubated with ADAMTS-4, the fluorescence recovered and fluorescence intensity markedly increased in proportion to concentrations of ADAMTS-4 and the probe. A nearly 3-fold increase in fluorescent intensity in response to only 3.9 pM of ADAMTS-4 was detected, whereas almost no fluorescence recovery was observed when the probe was incubated with matrix metalloproteinase (MMP)-1, -3, and -13. These results indicate a relative high sensitivity and specificity of the probe. Moreover, ADAMTS-4-D-Au probe was used to detect ADAMTS-4 activity in synovial fluid from 11 knee surgery patients. A substantial increase in fluorescent intensity was observed in the acute joint injury group as compared to the chronic joint injury and end-stage OA groups, indicating that this simple and low-cost sensing system might serve as a new detection method for ADAMTS-4 activity in biological samples and in screens for inhibitors for ADAMTS-4-related joint diseases. Additionally, this probe could be a potential biomarker for early diagnosis of cartilage-degrading joint diseases.

摘要

一种解整合素金属蛋白酶与凝血酶反应素-4(ADAMTS-4)在降解聚集蛋白聚糖(aggrecan)中起着关键作用,聚集蛋白聚糖是骨关节炎(OA)等关节疾病软骨降解的早期事件。检测 ADAMTS-4 的活性可为这些疾病的早期诊断和疾病修饰治疗提供有用的临床信息。因此,我们通过将 FITC 修饰的 ADAMTS-4 特异性肽(DVQEFRGVTAVIR)与金纳米粒子缀合,开发了一种 ADAMTS-4 检测荧光开启的 AuNP 探针(ADAMTS-4-D-Au 探针)。当 ADAMTS-4-D-Au 探针与 ADAMTS-4 孵育时,荧光恢复,荧光强度与 ADAMTS-4 和探针的浓度成正比显著增加。仅检测到 3.9 pM 的 ADAMTS-4 时,荧光强度增加近 3 倍,而当探针与基质金属蛋白酶(MMP)-1、-3 和 -13 孵育时,几乎没有荧光恢复。这些结果表明该探针具有相对较高的灵敏度和特异性。此外,还使用 ADAMTS-4-D-Au 探针检测了 11 例膝关节手术患者滑液中的 ADAMTS-4 活性。与慢性关节损伤和终末期 OA 组相比,急性关节损伤组的荧光强度显著增加,表明这种简单且低成本的传感系统可能成为生物样品中 ADAMTS-4 活性以及 ADAMTS-4 相关关节疾病抑制剂筛选的新检测方法。此外,该探针可能是软骨降解性关节疾病早期诊断的潜在生物标志物。

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