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用于骨密度生物标志物的适配体筛选与适配体传感器构建

Aptamer selection and aptasensor construction for bone density biomarkers.

作者信息

Chinnappan Raja, Zaghloul Norhan Sameh, AlZabn Razan, Malkawi Abeer, Abdel Rahman Anas, Abu-Salah Khalid M, Zourob Mohammed

机构信息

Department of Chemistry, Alfaisal University, Al Zahrawi Street, Al Maather, Al Takhassusi Rd, Riyadh, 11533, Saudi Arabia.

Department of Cellular Therapy and Cancer Research-Nanomedicine Section, King Abdullah International Medical Research Center/ King Saud Bin Abdulaziz University for Health Sciences, Ministry of the National Guard-Health Affairs, Riyadh, Saudi Arabia.

出版信息

Talanta. 2021 Mar 1;224:121818. doi: 10.1016/j.talanta.2020.121818. Epub 2020 Oct 29.

Abstract

Osteoporosis (OP) is a bone disease involved in dysregulation of one of the bone metabolism arms, formation, or desorption cause a porous bone. Osteocalcin (OC) and beta-crosslap (BC), are the well-known markers for OP, which are connected to bone formation and desorption, respectively. In addition to the OP biomarker, BC is also used as an estrogen replacement therapeutic monitoring. ELISA and other antibody-based detection methods are routinely used for measuring OC and BC. These methods have limitations that include thermostability, sensitivity, sacrificing animals, and cost of production. However, aptamer-based-assays are of interest to overcome these drawbacks and achieve the most specific and robust application. Herein, specific aptamers for OC and BC were selected by the systematic evolution of ligands by exponential enrichment (SELEX) method from the pool of ssDNA library with 60 random sequences. The binding affinity (K) of the selected aptamers were evaluated against the respective biomarkers. The high-affinity aptamers of OC and BC showed the K values of 59 and 55 nM respectively. A graphene oxide-based aptasensors were fabricated from the high-affinity aptamers, and the detection limits of OC and BC were found to be 0.4 pg/ml and 0.21 pg/ml, respectively. These aptasensors have been tested with OC and BC spiked buffer samples and validated using serum samples collected from osteoporotic rats.

摘要

骨质疏松症(OP)是一种涉及骨代谢分支之一失调的骨病,骨形成或骨吸收异常会导致骨多孔。骨钙素(OC)和β-交联氨基末端肽(BC)是众所周知的OP标志物,分别与骨形成和骨吸收相关。除了作为OP生物标志物外,BC还用于雌激素替代治疗监测。酶联免疫吸附测定(ELISA)和其他基于抗体的检测方法通常用于测量OC和BC。这些方法存在局限性,包括热稳定性、灵敏度、动物牺牲以及生产成本。然而,基于适配体的检测方法有望克服这些缺点并实现最特异、最可靠的应用。在此,通过指数富集配体系统进化(SELEX)方法,从具有60个随机序列的单链DNA文库中筛选出针对OC和BC的特异性适配体。评估所选适配体与各自生物标志物的结合亲和力(K)。OC和BC的高亲和力适配体的K值分别为59 nM和55 nM。用高亲和力适配体制备了基于氧化石墨烯的适配体传感器,发现OC和BC的检测限分别为0.4 pg/ml和0.21 pg/ml。这些适配体传感器已用添加了OC和BC的缓冲液样本进行测试,并使用从骨质疏松大鼠采集的血清样本进行了验证。

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