Production and engineering of nanobody‐based quenchbody sensors for detecting recombinant human growth hormone and its isoforms

Author:

Jung Jaehoon12,Jeong Yujin13,Xu Yinglan1,Yi Joonyeop14,Kim Minyoung1,Jeong Hee‐Jin5,Shin Sang Hoon6,Yang Yung‐Hun2,Son Junghyun1ORCID,Sung Changmin1ORCID

Affiliation:

1. Doping Control Center Korea Institute of Science and Technology Seoul Republic of Korea

2. Department of Microbial Engineering, College of Engineering Konkuk University Seoul Republic of Korea

3. Department of Bioengineering Hanyang University Seoul Republic of Korea

4. Interdisciplinary Program of Bioengineering Seoul National University Seoul Republic of Korea

5. Department of Biological and Chemical Engineering Hongik University Sejong‐ro 2639 Sejong Republic of Korea

6. Department of Surgery Chonnam National University Hwasun Hospital Hwasun Republic of Korea

Abstract

AbstractDue to athletes' misuse of recombinant human growth hormone (rhGH) for performance improvement, the World Anti‐Doping Agency has designated rhGH as a prohibited substance. This study focuses on the development and improvement of a simple and fast rhGH detection method using a fluorescence‐incorporated antibody sensor “Quenchbody (Q‐body)” that activates upon antigen binding. Camelid‐derived nanobodies were used to produce stable Q‐bodies that withstand high temperatures and pH levels. Notably, pituitary human growth hormone (phGH) comprises two major isoforms, namely 22 and 20 kDa GH, which exist in a specific ratio, and the rhGH variant shares the same sequence as the 22 kDa GH isoform. Therefore, we aimed to discriminate rhGH abuse by analyzing its specific isoform ratio. Two nanobodies, NbPit (recognizing phGH) and NbRec (preferentially recognizing 22 kDa rhGH), were used to develop the Q‐bodies. Nanobody production in Escherichia coli involved the utilization of a vector containing 6xHis‐tag, and Q‐bodies were obtained using a maleimide‐thiol reaction between the N‐terminal of the cysteine tag and a fluorescent dye. The addition of tryptophan residue through antibody engineering resulted in increased fluorescence intensity (FI) (from 2.58‐fold to 3.04‐fold). The limit of detection (LOD) was determined using a fluorescence response, with TAMRA‐labeled NbRec successfully detecting 6.38 ng/ml of 22 kDa rhGH while unable to detect 20 kDa GH. However, ATTO520‐labeled NbPit detected 7.00 ng/ml of 20 kDa GH and 2.20 ng/ml 22 kDa rhGH. Q‐bodies successfully detected changes in the GH concentration ratio from 10 to 40 ng/ml in human serum within 10 min without requiring specialized equipment and kits. Overall, these findings have potential applications in the field of anti‐doping measures and can contribute to improved monitoring and enforcement of rhGH misuse, ultimately enhancing fairness and integrity in competitive sports.

Funder

Korea Institute of Science and Technology

Publisher

Wiley

Subject

Spectroscopy,Pharmaceutical Science,Environmental Chemistry,Analytical Chemistry

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