
<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/">
  <dc:format>application/pdf</dc:format>
  <dc:format>625323 bytes</dc:format>
  <dc:publisher>Hemijski fakultet, Srpsko biohemijsko društvo</dc:publisher>
  <dc:identifier>https://phaidrabg.bg.ac.rs/o:37113</dc:identifier>
  <dc:identifier>ISBN: 978-86-7220-136-9</dc:identifier>
  <dc:title xml:lang="eng">A highly optimized protocol for the isolation and purification of transferrin from human serum </dc:title>
  <dc:language>eng</dc:language>
  <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/legalcode</dc:rights>
  <dc:creator id="https://orcid.org/0000-0001-9705-3237">Četić, Danilo</dc:creator>
  <dc:creator id="https://orcid.org/0000-0001-6417-8711">Miljuš, Goran</dc:creator>
  <dc:creator id="https://orcid.org/0000-0002-3619-8472">Stevanović, Jovana</dc:creator>
  <dc:creator id="https://orcid.org/0000-0002-0898-5401">Dobrijević, Zorana</dc:creator>
  <dc:creator id="https://orcid.org/0000-0002-0940-9481">Šunderić, Miloš</dc:creator>
  <dc:creator id="https://orcid.org/0000-0003-2042-0056">Nedić, Olgica</dc:creator>
  <dc:creator>Gligorijević, Nikola</dc:creator>
  <dc:creator id="https://orcid.org/0000-0002-0898-5401">Vilotić, Aleksandra</dc:creator>
  <dc:creator>Borko, Valentina</dc:creator>
  <dc:creator>Gabričević, Mario</dc:creator>
  <dc:creator>Weitner, Tin</dc:creator>
  <dc:creator id="https://orcid.org/0000-0002-2539-4507">Penezić, Ana</dc:creator>
  <dc:description xml:lang="eng"> Different methods for the isolation and purification of human transferrin (Tf) from human plasma and se
rum have been described in the literature. However, none provide a highly pure final product in a time-ef
ficient manner, whereas the method described in this work accomplishes both. It consists of two separate 
steps—a sample preparation and an anion-exchange chromatography step.
Our initial methodology used rivanol for protein precipitation in the first step and activated charcoal 
for the removal of excess rivanol from the remaining supernate. This provided Tf of &gt;99% purity while 
retaining Tf function, analyzed by immunofluorescent staining for transferrin-transferrin receptor 1 in
teraction and ferrozine method for iron binding capacity, and structure, confirmed by recording and 
comparing fluorescent spectra of purified Tf and commercially available pure Tf. However, the method 
produced a relatively low Tf yield. The initial method was then modified to use potassium bromide for 
excess rivanol removal, increasing yield by approximately 82% compared to the initial protocol. We 
then tested if saturating Tf with iron(III) ions before precipitation with rivanol would increase yield. This 
increased yield by a further 20% compared to potassium bromide rivanol removal, and a final 119% 
compared to the initially proposed method. The improved method was additionally evaluated for the 
purification of Tf from the serum of patients with different iron-associated pathologies, showing its 
applicability on different types of samples.</dc:description>
  <dc:type>info:eu-repo/semantics/conferenceProceedings</dc:type>
  <dc:date>2025</dc:date>
  <dc:source>A highly optimized protocol for the isolation and purification of transferrin from human serum </dc:source>
  <dc:source>startpage: 135</dc:source>
  <dc:source>endpage: 136</dc:source>
  <dc:subject xml:lang="eng">transferrin, anion-exchange chromatography, protein purification</dc:subject>
</oai_dc:dc>
