| Literature DB >> 29594592 |
Najmeh Ansari1, Kiarash Ghazvini2, Mohammad Ramezani3, Mahin Shahdordizadeh4, Rezvan Yazdian-Robati4, Khalil Abnous5, Seyed Mohammad Taghdisi6.
Abstract
The Mycobacterium Ag85 complex is the major secretory protein of M. tuberculosis. It is a potential marker for early diagnosis of tuberculosis (TB). The authors have identified specific aptamers for Ag85A (FbpA) via protein SELEX using magnetic beads. After twelve rounds of selection, two aptamers (Apt8 and Apt22) were chosen from different groups, and their binding constants were determined by flow cytometry. Apt22 (labeled with Atto 647N) binds to FbpA with high affinity (Kd = 63 nM) and specificity. A rapid, sensitive, and low-cost fluorescent assay was designed based on the use of Apt22 and graphene oxide, with a limit of detection of 1.5 nM and an analytical range from 5 to 200 nM of FbpA. Graphical abstract Schematic illustration of graphene oxide-based aptasensor for fluorometric determination of FbpA.Entities:
Keywords: Fluorescent assay; Limit of detection; Quenching; SELEX; Secretory protein; Serum
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Year: 2017 PMID: 29594592 DOI: 10.1007/s00604-017-2550-3
Source DB: PubMed Journal: Mikrochim Acta ISSN: 0026-3672 Impact factor: 5.833