E-ISSN: 2477-054X P-ISSN: 1907-3879 Open Access
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Open Access Peer Reviewed

PENGEMBANGAN MARKER MULTIEPITOP UNTUK KIT DIAGNOSTIK HPV E6 BERBASIS LATERAL FLOW ASSAY MELALUI PENDEKATAN IN SILICO

Nadifah Hasna (Politeknik Kesehatan Kementerian Kesehatan Bandung)
Sabrina Rizki Febriyanti (Politeknik Kesehatan Kementerian Kesehatan Bandung)
Taniani Alginta (Politeknik Kesehatan Kementerian Kesehatan Bandung)
Shafira Syifa Aprilia (Politeknik Kesehatan Kementerian Kesehatan Bandung)
Ghaisani Fitri Sajidah (Politeknik Kesehatan Kementerian Kesehatan Bandung)
Salsabila (Politeknik Kesehatan Kementerian Kesehatan Bandung)
Asep Iin Nur Indra (Politeknik Kesehatan Kementerian Kesehatan Bandung)
Article Publication History
Received 27 Mar 2025
Revised 04 Sep 2025
Accepted 04 Sep 2025
Published Online 05 Sep 2025
10.26874/jkkes.v20i2.441
419
281
Scholar Citations
114-124

Abstract

Background : Cervical cancer is the second most common cancer after breast cancer and has a high mortality rate from all cancer deaths. Cervical cancer has been proven to be caused by continuous infection of oncogenic types of Human papillomavirus (HPV), namely high-risk HPV types including types 31, 33, 35, and 58. In the HPV life cycle, the E6 protein plays a crucial role in regulating cellular functions that contribute to cell transformation into cancer. The E6 protein from HPV types functions as the main oncoprotein that plays a role in the process of immortalization and cell malignancy. Mechanistically, the E6 protein from high-risk HPV contributes to the inactivation of the p53 tumor suppressor protein. Objective : This study aims to develop a multiepitope marker based on the E6 protein as the main component in the Lateral Flow Assay (LFA. Method : diagnostic kit with a bioinformatics approach method to identify immunogenic and conservative B cell epitopes in the HPV E6 protein which are then cloned in silico in the pET-28a (+) plasmid, so that it can produce a diagnostic kit that is specific for detecting Human papillomavirus (HPV). Result : The results showed that the designed multiepitope marker has the ability to trigger an effective immune response against B cells and has a fairly strong interaction between antigen and antibody. This study also showed the ability of the E6 protein to be expressed on the pET-28a(+) plasmid. Conclusion : This study provides a strong basis for further development and evaluation in vivo studies for the development of lateral flow assay (LFA)-based screening diagnostic kits utilizing Recombinant DNA technology.