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Tuning of CHO secretional machinery improve activity of secreted therapeutic sulfatase 150-fold

Thalén, Niklas (author)
KTH,Proteinteknologi
Moradi, Mona (author)
KTH,Proteinteknologi
Lundqvist, Magnus (author)
KTH,Proteinteknologi
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Rodhe, Johanna (author)
SOBI AB, Tomtebodavagen 23A, Stockholm, Sweden, Tomtebodavägen 23A
Andersson, Monica (author)
SOBI AB, Tomtebodavagen 23A, Stockholm, Sweden, Tomtebodavägen 23A
Bidkhori, Gholamreza (author)
KTH,Science for Life Laboratory, SciLifeLab,Systembiologi,AIVIVO Ltd. Unit 25, Bio-innovation centre, Cambridge Science park, Cambridge, UK, Cambridge Science park
Possner, Dominik (author)
SOBI AB, Tomtebodavagen 23A, Stockholm, Sweden, Tomtebodavägen 23A
Su, Chao (author)
SOBI AB, Tomtebodavagen 23A, Stockholm, Sweden, Tomtebodavägen 23A
Nilsson, Joakim (author)
SOBI AB, Tomtebodavagen 23A, Stockholm, Sweden, Tomtebodavägen 23A
Eisenhut, Peter (author)
ACIB - Austrian Centre of Industrial Biotechnology, Krenngasse 37, 8010 Graz, Austria, Krenngasse 37; BOKU - University of Natural Resources and Life Sciences, Department of Biotechnology, Vienna, 1190, Austria
Malm, Magdalena, 1983- (author)
KTH,Proteinteknologi
Karlsson, Alice (author)
KTH,Proteinteknologi
Vestin, Jeanette (author)
SOBI AB, Tomtebodavagen 23A, Stockholm, Sweden, Tomtebodavägen 23A
Forsberg, Johan (author)
SOBI AB, Tomtebodavagen 23A, Stockholm, Sweden, Tomtebodavägen 23A
Nordling, Erik (author)
SOBI AB, Tomtebodavagen 23A, Stockholm, Sweden, Tomtebodavägen 23A
Mardinoglu, Adil (author)
KTH,Science for Life Laboratory, SciLifeLab,Systembiologi
Volk, Anna-Luisa (author)
KTH,Proteinteknologi
Sandegren, Anna (author)
SOBI AB, Tomtebodavagen 23A, Stockholm, Sweden, Tomtebodavägen 23A
Rockberg, Johan (author)
KTH,Proteinteknologi
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 (creator_code:org_t)
Elsevier BV, 2024
2024
English.
In: Metabolic engineering. - : Elsevier BV. - 1096-7176 .- 1096-7184. ; 81, s. 157-166
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Rare diseases are, despite their name, collectively common and millions of people are affected daily of conditions where treatment often is unavailable. Sulfatases are a large family of activating enzymes related to several of these diseases. Heritable genetic variations in sulfatases may lead to impaired activity and a reduced macromolecular breakdown within the lysosome, with several severe and lethal conditions as a consequence. While therapeutic options are scarce, treatment for some sulfatase deficiencies by recombinant enzyme replacement are available. The recombinant production of such sulfatases suffers greatly from both low product activity and yield, further limiting accessibility for patient groups. To mitigate the low product activity, we have investigated cellular properties through computational evaluation of cultures with varying media conditions and comparison of two CHO clones with different levels of one active sulfatase variant. Transcriptome analysis identified 18 genes in secretory pathways correlating with increased sulfatase production. Experimental validation by upregulation of a set of three key genes improved the specific enzymatic activity at varying degree up to 150-fold in another sulfatase variant, broadcasting general production benefits. We also identified a correlation between product mRNA levels and sulfatase activity that generated an increase in sulfatase activity when expressed with a weaker promoter. Furthermore, we suggest that our proposed workflow for resolving bottlenecks in cellular machineries, to be useful for improvements of cell factories for other biologics as well.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinsk bioteknologi -- Medicinsk bioteknologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Medical Biotechnology -- Medical Biotechnology (hsv//eng)

Keyword

CHO
Sulfatase
Systems biology
Transcriptomics

Publication and Content Type

ref (subject category)
art (subject category)

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