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PMID: 2415396 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Isolation of a cDNA clone for a catalytic subunit of Torpedo marmorata acetylcholinesterase.

FEBS letters ·Vol. 193 ·No. 2 ·1985-12-02 ·Pages 159-63

Sikorav JL, Vallette F, Grassi J, Massoulié J

Abstract

We have constructed a cDNA library from Torpedo marmorata electric organ poly(A+) RNA in the lambda phage expression vector lambda gt11. This library has been screened with polyclonal anti-acetylcholinesterase antibodies. One clone, lambda AChE1, produced a fusion protein which was recognized by the antibodies and which prevented the binding of native acetylcholinesterase in an enzymatic immune assay. These results indicate that lambda AChE1 contains a cDNA insert coding for a part of a catalytic subunit of Torpedo acetylcholinesterase. The 200-base-pair cDNA insert hybridized to three mRNAs (14.5, 10.5 and 5.5 kb) from Torpedo electric organs. These mRNAs were also detected in Torpedo electric lobes.

MeSH Terms
Acetylcholinesterase/genetics Animals Catalysis Cloning, Molecular DNA/isolation & purification Electrophoresis, Agar Gel Immunochemistry Nucleic Acid Hybridization Poly A RNA RNA, Messenger Torpedo
Chemicals
RNA, Messenger Poly A RNA DNA Acetylcholinesterase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Sikorav J L
Vallette F
Grassi J
Massoulié J
Article Info
Journal
FEBS letters
Abbr.
FEBS Lett
ISSN
0014-5793
Published
1985-12-02
Pages
159-63
Language
English
Region
England
NLM ID
0155157
Subset
IM
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