Abstract
Background: Cystinosis is a rare inherited lysosomal storage disease (LSD), caused by
a mutation in the Cystinosin Lysosomal Cystine Transporter (CTNS). Novel therapies and strategies
are needed to improve patients' clinical conditions and quality of life.
Objectives and Methods: This study assessed whether CTNS can be secreted, and investigated a
method to enhance its secretion, by adding a secretion signal to the N-terminus. Human Embryonic
Kidney (HEK) 293 cells were transfected with the resulting construct. The amount of protein
secreted was then measured. Uptake by monolayer cultures of cystinotic cells and enzyme activity
were also assessed.
Results: The recombinant protein could effectively be secreted, and the secretion signal slightly
further increased its secretion. The secreted recombinant protein was taken up by cystinotic cells,
and, after internalization, still retained its biological activity.
Conclusion: Optimization of the proposed method to increase the secretion of CTNS would provide
new insights into the production of recombinant proteins for medical and industrial use. Further
identification and screening of alternative signalling peptides and cell types can maximise the
secretion and production of recombinant CNTS, to be used as a therapeutic agent in human
healthcare.
Graphical Abstract
[4]
Castro-Balado A, Mondelo-García C, Varela-Rey I, et al. Recent research in ocular cystinosis: Drug delivery systems, cysteamine detection methods and future perspectives. Pharmaceutics 2020; 12(12): 1177.
[5]
Elmonem MA, Veys KRP, Prencipe G. Nephropathic cystinosis: Pathogenic roles of inflammation and potential for new therapies. Cells 2022; 11(2): 190.
[12]
Wang JY. Improving the secretion of designed protein assemblies through negative design of cryptic transmembrane domains. In: Daniel WK, Ed. Center for HIV/AIDS Vaccine Immunology and Immunogen Discovery. La Jolla, CA: The Scripps Research Institute 2023.
[21]
Massaro G, Geard AF, Liu W. Gene therapy for lysosomal storage disorders: Ongoing studies and clinical development. Biomolecules 2021; 11(4): 611.
[64]
Sekar A, Santhanam A, Sandhu C. Area under the curve spectrophotometric method for determination of irbesatran in pharmaceutical formulation. IRA-Int J Appl Sci 2017; 7(2): 95.
[67]
Gadhave M, Jadhav S, Gaikwad D, et al. Area under curve by UV spectrophotometric method for determination of ascorbic acid in bulk. Bull Env Pharmacol Life Sci 2020; 9(8): 35-9.
[68]
Dhumane S, Patel S, Kedar V. Area under curve by uv spectrophotometric method for determination aloe vera gel powder in bulk. SSRN 2020; 7(1)
[69]
Karpova S, Blazheyevskiy M, Mozgova O. Development and validation of UV Spectrophotometric area under curve method quantitative estimation of piperacillin. Int J Pharm Sci Res 2018; 9: 3556-60.