Home LiteratureArticle Details
PMID: 2007607 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Characterization of human loricrin. Structure and function of a new class of epidermal cell envelope proteins.

The Journal of biological chemistry ·Vol. 266 ·No. 10 ·1991-04-05 ·Pages 6626-36

Hohl D, Mehrel T, Lichti U, Turner ML, Roop DR, Steinert PM

Abstract

We have isolated and characterized a full-length cDNA clone encoding human loricrin. Curiously, this protein displays major differences from the recently described mouse loricrin (Mehrel, T., Hohl, D., Nakazawa, H., Rothnagel, J.A., Longley, M.A., Bundman, D., Cheng, C.K., Lichti, U., Bisher, M.E., Steven, A. C., Steinert, P.M., Yuspa, S.H., and Roop, D.R. (1990) Cell 61, 1103-1112). Although both proteins are glycine-serine-cysteine-rich, the sequences have not been conserved. However, analysis of the sequences reveals a common motif of quasi-peptide repeats of an aliphatic or aromatic amino acid residue followed by several glycine and/or serine and cysteine residues. These sequences are interspersed and flanked by short glutamine- or glutamine/lysine-rich peptides. Thus loricrins consist of a family of cell envelope proteins of highly variable sequences that nevertheless retain common structural elements. We show that unlike all other putative protein components of the cell envelope, loricrins are highly insoluble, due at least in part to cross-linking by disulfide bonds. Furthermore, we have isolated four peptides from purified human cell envelopes that contain recognizable loricrin sequences and which are cross-linked by the N epsilon-(gamma-glutamyl)lysine isodipeptide bond. The presence of such bonds thus affords an explanation for the extraordinary insolubility of loricrin by cross-linking to the cell envelope and can also explain the low steady-state levels of monomeric loricrin in cytoskeletal extracts of epidermis. This study represents the first report of this isodipeptide cross-link in a protein component of the cornified cell envelope. We propose a model for the structure of loricrin in which (i) the unusual glycine-serine-rich sequences adopt a flexible loop conformation, indexed on the recurrent aliphatic residues; (ii) inter- or intramolecular isodipeptide and disulfide cross-links induce or stabilize folding of loricrin so as to form a more compact rosette-like structure; and (iii) the presence of the flexible glycine-rich loops necessarily will impact a flexible character to the cell envelope and entire epithelium.

MeSH Terms
Amino Acid Sequence Amino Acids/analysis Base Sequence Blotting, Northern DNA/genetics Epidermis/metabolism Fluorescent Antibody Technique Humans Membrane Proteins/genetics,metabolism Molecular Sequence Data Nucleic Acid Hybridization Protein Biosynthesis RNA, Messenger/analysis,genetics
Chemicals
Amino Acids Membrane Proteins RNA, Messenger loricrin DNA
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Hohl D
Dermatology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892.
Mehrel T
Lichti U
Turner M L
Roop D R
Steinert P M
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1991-04-05
Pages
6626-36
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Databases
GENBANK
D90272, M59186, M59187, M59188, M59189, M60203, M60204, M60205, M60206, M61120
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]