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Cloning and expression of human lecithin-cholesterol acyltransferase cDNA.

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McLean, J, Fielding, C, Drayna, D, Dieplinger, H, Baer, B, Kohr, W, Henzel, W, Lawn, R·1986·Proceedings of the National Academy of Sciences

Abstract

cDNA and genomic cloning has been used to determine the mRNA and amino acid sequence of human plasma lecithin-cholesterol acyltransferase (LCATase; EC 2.3.1.43). The mature protein was found to contain 416 amino acid residues with a hydrophobic leader sequence of 24 amino acids. An unusual feature of the message is that the poly(A) signal AATAAA overlaps the COOH-terminal glutamic acid and stop codons, and the 3' untranslated region is only 23 bases. The protein itself is distinguished by a number of extended sequences of hydrophobic amino acids, one of which contains a hexapeptide identical with the interfacial binding segment of the active site of pancreatic lipase and is similar to the same site of lingual lipase. The cloned cDNA allows the expression of active LCATase by transfected tissue culture cells.

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Metadata

Authors
McLean, J., Fielding, C., Drayna, D., Dieplinger, H., Baer, B., Kohr, W., Henzel, W., & Lawn, R.
Venue
Proceedings of the National Academy of Sciences
Published
1986-04
Volume
83
Issue
8
Pages
2335-2339
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2033168374
Cited by
164
References
0
FWCI
19.44
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Cloning and expression of human lecithin-cholesterol acyltransferase cDNA. https://app.cochat.ai/papers/10.1073/pnas.83.8.2335
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McLean, J., Fielding, C., Drayna, D., Dieplinger, H., Baer, B., Kohr, W., Henzel, W., & Lawn, R. (1986). Cloning and expression of human lecithin-cholesterol acyltransferase cDNA. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.83.8.2335

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