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PMID: 9233640 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Evidence that the two C1q binding membrane proteins, gC1q-R and cC1q-R, associate to form a complex.

Journal of immunology (Baltimore, Md. : 1950) ·Vol. 159 ·No. 3 ·1997-08-01 ·Pages 1429-36

Ghebrehiwet B, Lu PD, Zhang W, Keilbaugh SA, Leigh LE, Eggleton P, Reid KB, Peerschke EI

Abstract

Two types of widely coexpressed, highly acidic, cell membrane binding proteins that display preferential domain specificity for C1q have been described: a 60-kDa calreticulin homologue, designated cC1q-R, that binds to the collagen-like "stalk" and a 33-kDa glycoprotein with affinity for the globular "heads" (gC1q-R). Although the two molecules are known to be coexpressed on all cell types examined to date and often coelute during purification, there is no direct evidence showing that they associate with each other either on the membrane or when examined in a purified system. In this report we present the first evidence that 1) biotinylated cC1q-R binds to recombinant as well as native gC1q-R, as assessed by solid phase ELISA; 2) binding sites for cC1q-R are located within N-terminal residues 76 through 93 of the mature form of gC1q-R and within residues 204 through 218; 3) this interaction is inhibited by two mAbs, 60.11 and 46.23, that recognize primarily epitopes within the N terminus of gC1q-R corresponding to residues 74 through 96 and by mAb 74.5.2 that recognizes epitopes within residues 204 through 218; and 4) biotinylated cC1q-R binds to microtiter-fixed Raji and K562 cells, and this interaction is inhibited by mAb 60.11. Furthermore, coimmunoprecipitation analysis of Raji cell membranes with anti-gC1q-R mAbs showed the presence of cC1q-R in addition to gC1q-R. Taken together, the evidence suggests that cC1q-R is able to form a complex with gC1q-R and may associate with gC1q-R on the cell surface.

MeSH Terms
Amino Acid Sequence Antibodies, Monoclonal/pharmacology Binding, Competitive/immunology Biopolymers/chemistry,immunology,metabolism Biotin/metabolism Carrier Proteins Complement C1q/metabolism Enzyme-Linked Immunosorbent Assay Humans Hyaluronan Receptors Membrane Glycoproteins/chemistry,immunology,metabolism Mitochondrial Proteins Molecular Sequence Data Phosphatidylinositols/metabolism Protein Binding/immunology Receptors, Complement/chemistry,immunology,metabolism Subcellular Fractions/immunology,metabolism Tumor Cells, Cultured
Chemicals
Antibodies, Monoclonal Biopolymers C1QBP protein, human Carrier Proteins Hyaluronan Receptors Membrane Glycoproteins Mitochondrial Proteins Phosphatidylinositols Receptors, Complement complement 1q receptor Biotin Complement C1q
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Ghebrehiwet B
Department of Medicine, State University of New York, Stony Brook 11794, USA. berhane@epo.som.sunysb.edu
Lu P D
Zhang W
Keilbaugh S A
Leigh L E
Eggleton P
Reid K B
Peerschke E I
Article Info
Journal
Journal of immunology (Baltimore, Md. : 1950)
Abbr.
J Immunol
ISSN
0022-1767
Published
1997-08-01
Pages
1429-36
Language
English
Region
United States
NLM ID
2985117R
Subset
IM
Grants
NHLBI NIH HHS · R01HL5029101 · United States
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