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Studies on cysteine-rich peptides from Nemertea and Violaceae [Elektronisk resurs] Proteomic and transcriptomic discovery and characterization

Jacobsson, Erik, 1986- (författare)
Göransson, Ulf, 1970- (preses)
Andersson, Håkan S. (preses)
Burman, Robert, 1979- (preses)
Hansen, Espen (opponent)
Farmakognosi (medarbetare)
Uppsala universitet Medicinska och farmaceutiska vetenskapsområdet (utgivare)
Uppsala universitet Medicinska och farmaceutiska vetenskapsområdet (utgivare)
Publicerad: Uppsala : Acta Universitatis Upsaliensis, 2019
Engelska.
Serie: Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Pharmacy, 1651-6192 1651-6192 ; 277
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  • E-bokAvhandling(Diss. (sammanfattning) Uppsala : Uppsala universitet, 2019)
Sammanfattning Ämnesord
Stäng  
  • The overall aims of the projects included in this thesis were to discover, synthesize and characterize disulphide-stabilized peptides from marine worms ( Nemertea sp.) and plants ( Viola sp.).  One of the main outcomes of this thesis is the discovery of a new family of highly active cysteine-rich toxins, alpha nemertides, from nemertean worms (paper II) . Functional characterization and production routes of nemertides were further explored (papers II-III ). In addition, 12 new cyclotides from the bog violet were discovered (paper I) . Finally, transcriptomes and mucus of the Antarctic nemertean Parborlasia corrugatus were investigated for toxin content (paper IV) .  In paper I wild-type leaf and callus tissue of the endangered bog violet, V. uliginosa , were analyzed using transcriptomics and LC-MS, resulting in the discovery of 12 new cyclotides (i.e. cysteine-rich cyclic peptides). In addition, cyclotide expression under different cell-growth conditions was monitored. In paper II  the discovery and initial characterization of a new family of highly active peptides, the alpha nemertides, from the epidermal mucus of the world’s longest animal; Lineus longissimus is described. The most abundant alpha nemertide, alpha-1, was extracted in minute amounts, prompting the use solid phase peptide synthesis (SPPS) for further characterization. The tertiary structure of alpha-1 was elucidated and revealed an inhibitory cystine knot (ICK) framework. The knotted core-structure is similar to the cyclic cystine knot (CCK) motif, found in the cyclotides described in paper I . In manuscript III , the production route established in paper II was used to produce nemertides alpha 1-7. These were tested in vivo in an Artemia microwell assay as well as on an extended panel of voltage-gated sodium channels (Na V 1.1 – 1.8 and BgNa V 1). All seven alpha nemertides were highly active in the in vivo Artemia assay with EC 50 values in the sub to low µM range. The alpha nemertides were also active in the Na V s tested. However, differences in the activity profiles were observed, indicating an opportunity for future optimization of alpha nemertides to reach higher specificity to certain Na V subtypes. In manuscript IV, the exploration of nemertide toxins was extended to include the Antarctic P. corrugatus . Resulting findings include a set of cysteine-rich peptides, some similar to the nemertides previously discovered in paper II . Two purified peptides and one fraction were evaluated for their membranolytic activity. 

Ämnesord

Medical and Health Sciences  (hsv)
Basic Medicine  (hsv)
Pharmacology and Toxicology  (hsv)
Medicin och hälsovetenskap  (hsv)
Medicinska och farmaceutiska grundvetenskaper  (hsv)
Farmakologi och toxikologi  (hsv)
Farmakognosi  (uu)
Pharmacognosy  (uu)
Farmakognosi  (uu)
Pharmacognosy  (uu)
Farmakognosi  (uu)
Pharmacognosy  (uu)
Farmakognosi  (uu)
Pharmacognosy  (uu)
Farmaceutisk vetenskap  (uu)
Pharmaceutical Science  (uu)
Farmaceutisk vetenskap  (uu)
Pharmaceutical Science  (uu)
Farmaceutisk vetenskap  (uu)
Pharmaceutical Science  (uu)

Genre

government publication  (marcgt)

Indexterm och SAB-rubrik

Peptide toxin
cystine knot
nemertide
cyclotide
nemertea.
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