Document 0079 DOCN M94A0079 TI Use of TrpE fusion protein to identify antigenic domains within the BIV envelope protein. DT 9412 AU Chen P; Liu ZQ; Wood C; Department of Microbiology, University of Kansas, Lawrence 66045. SO J Virol Methods. 1994 May;47(3):331-43. Unique Identifier : AIDSLINE MED/94351053 AB Nine different recombinant clones spanning various regions of the bovine immunodeficiency-like virus (BIV) envelope gene open reading frame were generated. These clones span the entire external glycoprotein as well as the transmembrane glycoprotein region. These proteins were expressed as fusions to the TrpE protein in E. coli. The levels of recombinant protein expressed varied, some clones expressed enough protein that can be detected in a Coomassie blue-stained gel, whereas other proteins could only be detected by Western blot analyses. A recombinant env protein representing the extracellular domain of the env protein was detected by BIV-infected bovine sera. In addition, a 134 amino acid peptide which may represent a major immunoreactive epitope was identified. This peptide is located at the amino terminus of the transmembrane glycoprotein and was specifically recognized by all BIV-infected calf sera tested. The identification of this epitope and the use of recombinant envelope protein will enable us to develop a more effective screening test to study the epidemiology of BIV infection. DE Animal Antigenic Determinants/*ANALYSIS Cattle Cloning, Molecular Escherichia coli/GENETICS Immunoblotting Immunodeficiency Virus, Bovine/GENETICS/*IMMUNOLOGY Lentivirus Infections/MICROBIOLOGY Recombinant Fusion Proteins/GENETICS/IMMUNOLOGY Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. Viral Envelope Proteins/GENETICS/*IMMUNOLOGY JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).