Next Article in Journal
Rethinking ME/CFS Diagnostic Reference Intervals via Machine Learning, and the Utility of Activin B for Defining Symptom Severity
Previous Article in Journal
Prevalence of Oral Lesions and Correlation with Intestinal Symptoms of Inflammatory Bowel Disease: A Systematic Review

Ultrasensitive ELISA Developed for Diagnosis

Department of Biology, Waseda University, Tokyo 162-8480, Japan
R&D Headquarters, TAUNS Laboratories, Inc., Shizuoka 410-2325, Japan
Waseda Research Institute for Science and Engineering, Waseda University, Tokyo 162-8480, Japan
Department of Medical Laboratory Science and Biotechnology, Kaohsiung Medical University, Kaohsiung 80756, Taiwan
School of Pharmaceutical Sciences, Health Sciences University of Hokkaido, Hokkaido 061-0293, Japan
Graduate Institute of Medicine, School of Medicine, Kaohsiung Medical University, Kaohsiung 80756, Taiwan
Author to whom correspondence should be addressed.
These authors contributed equally to this work.
Diagnostics 2019, 9(3), 78;
Received: 24 May 2019 / Revised: 4 July 2019 / Accepted: 16 July 2019 / Published: 18 July 2019
(This article belongs to the Section Point-of-Care Diagnostics and Devices)
For the diagnosis of disease, the ability to quantitatively detect trace amounts of the causal proteins from bacteria/viruses as biomarkers in patient specimens is highly desirable. Here we introduce a simple, rapid, and colorimetric assay as a de novo, ultrasensitive detection method. This ultrasensitive assay consists of a sandwich enzyme-linked immunosorbent assay (ELISA) and thionicotinamide-adenine dinucleotide (thio-NAD) cycling, forming an ultrasensitive ELISA, in which the signal substrate (i.e., thio-NADH) accumulates in a triangular manner, and the accumulated thio-NADH is measured at its maximum absorption wavelength of 405 nm. We have successfully achieved a limit of detection of ca. 10−18 moles/assay for a target protein. As an example of infectious disease detection, HIV-1 p24 could be measured at 0.0065 IU/assay (i.e., 10−18 moles/assay), and as a marker for a lifestyle-related disease, adiponectin could be detected at 2.3 × 10−19 moles/assay. In particular, despite the long-held belief that the trace amounts of adiponectin in urine can only be detected using a radioisotope, our ultrasensitive ELISA was able to detect urinary adiponectin. This method is highly versatile because simply changing the antibody enables the detection of various proteins. This assay system requires only the measurement of absorbance, thus it requires equipment that is easily obtained by medical facilities, which facilitates diagnosis in hospitals and clinics. Moreover, we describe an expansion of our ultrasensitive ELISA to a non-amplification nucleic acid detection method for nucleic acids using hybridization. These de novo methods will enable simple, rapid, and accurate diagnosis. View Full-Text
Keywords: adiponectin; diagnosis; HIV; insulin; non-amplification nucleic acid detection; ultrasensitive ELISA adiponectin; diagnosis; HIV; insulin; non-amplification nucleic acid detection; ultrasensitive ELISA
Show Figures

Graphical abstract

MDPI and ACS Style

Iha, K.; Inada, M.; Kawada, N.; Nakaishi, K.; Watabe, S.; Tan, Y.H.; Shen, C.; Ke, L.-Y.; Yoshimura, T.; Ito, E. Ultrasensitive ELISA Developed for Diagnosis. Diagnostics 2019, 9, 78.

AMA Style

Iha K, Inada M, Kawada N, Nakaishi K, Watabe S, Tan YH, Shen C, Ke L-Y, Yoshimura T, Ito E. Ultrasensitive ELISA Developed for Diagnosis. Diagnostics. 2019; 9(3):78.

Chicago/Turabian Style

Iha, Kanako, Mikio Inada, Naoki Kawada, Kazunari Nakaishi, Satoshi Watabe, Yong H. Tan, Chieh Shen, Liang-Yin Ke, Teruki Yoshimura, and Etsuro Ito. 2019. "Ultrasensitive ELISA Developed for Diagnosis" Diagnostics 9, no. 3: 78.

Find Other Styles
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

Back to TopTop