The major structural protein (VP1) of the BK polyomavirus (BKV) was express
ed in the recombinant baculovirus expression system. Recombinant BKV VP1 wa
s shown to self-assemble into virus-like particles (VLPs) with a diameter o
f 45-50 rim. As for other polyomaviruses, BKV VP1 has the capacity to bind
to exogenous DNA. Furthermore, the potential of BKV VP1 VLPs was investigat
ed for gene transfer into COS-7 cells using three methods for the formation
of pseudo-virions: disassembly/reassembly, osmotic shock and direct intera
ction between VLPs and reporter plasmid DNA. The latter method was shown to
be the most efficient when using linearized plasmid. Gene transfer efficie
ncy with BKV pseudo-virions was of the same order as that observed with hum
an papillomavirus type 16 L1 protein VLPs. In addition, it is demonstrated
that cellular entry of BKV pseudo-virions is dependent on cell surface sial
ic acid.