Comparative incorporation of glycoproteins B, C, and D into mutant virus envelopes. [35S]methionine/cysteine-labeled sucrose-purified KOS (A), KgBpK− (B), KCZ (C), KgBpK−gC− (D), KgBpK−gCR (E), and KgBpKRgC− (F) viruses were solubilized with detergent and immunoprecipitated with a pool of MAbs directed against gB (lanes 1), gC (lanes 2), or gD (lanes 3). The immune complexes were captured on protein A-Sepharose, resuspended in Laemmli buffer, and separated by SDS-PAGE. Asterisks indicate the positions of the glycoproteins designated on the left, when present.