دورية أكاديمية

Synthesis, processing, and secretion of rat immunoglobulin E made in Xenopus oocytes.

التفاصيل البيبلوغرافية
العنوان: Synthesis, processing, and secretion of rat immunoglobulin E made in Xenopus oocytes.
المؤلفون: Lund T, Bravo R, Johansen HR, Zeuthen J, Vuust J
المصدر: FEBS letters [FEBS Lett] 1986 Nov 24; Vol. 208 (2), pp. 369-72.
نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't
اللغة: English
بيانات الدورية: Publisher: John Wiley & Sons Ltd Country of Publication: England NLM ID: 0155157 Publication Model: Print Cited Medium: Print ISSN: 0014-5793 (Print) Linking ISSN: 00145793 NLM ISO Abbreviation: FEBS Lett Subsets: MEDLINE
أسماء مطبوعة: Publication: Jan. 2016- : West Sussex : John Wiley & Sons Ltd.
Original Publication: Amsterdam, North-Holland on behalf of the Federation of European Biochemical Societies.
مواضيع طبية MeSH: Immunoglobulin E/*biosynthesis, Animals ; Glycosylation ; Immunoglobulin E/metabolism ; Microinjections ; Molecular Weight ; Oocytes/metabolism ; Protein Biosynthesis ; Protein Processing, Post-Translational ; RNA, Messenger/genetics ; Rats ; Xenopus laevis
مستخلص: Rat immunoglobulin E (IgE) synthesized in Xenopus laevis oocytes, injected with rat plasmacytoma mRNA, was analysed by specific immunoprecipitation and SDS-polyacrylamide gel electrophoresis under reducing as well as non-reducing conditions. The results indicate that the oocytes will translate and correctly process the rat IgE heavy and light chains, resulting in secretion of a correctly assembled, normal immunoglobulin molecule. The normal, extensive glycosylation of the IgE heavy chain (e-chain) is faithfully carried out by the oocytes; therefore, this posttranslational modification is apparently of an unspecific nature, and does not depend upon a mechanism specific for plasma cells.
المشرفين على المادة: 0 (RNA, Messenger)
37341-29-0 (Immunoglobulin E)
تواريخ الأحداث: Date Created: 19861124 Date Completed: 19870107 Latest Revision: 20190621
رمز التحديث: 20221208
DOI: 10.1016/0014-5793(86)81051-1
PMID: 3780973
قاعدة البيانات: MEDLINE
الوصف
تدمد:0014-5793
DOI:10.1016/0014-5793(86)81051-1