Antibody 64m-5 fab in complex with a double-stranded DNA (6-4) photoproduct
Structure:
Anti-(6-4) photoproduct antibody 64m-5 fab (light chain). Chain: l. Anti-(6-4) photoproduct antibody 64m-5 fab (heavy chain). Chain: h. DNA (5'-d( Gp Cp Gp Ap Gp Tp Gp Ap (64T)p (5Py) p Ap Tp Gp Gp Ap Cp Gp G)-3'). Chain: a. Engineered: yes. DNA (5'-
Source:
Mus musculus. Organism_taxid: 10090. Strain: balb/c. Other_details: hybridoma. Synthetic: yes. Other_details: DNA with (6-4) photoproduct. Other_details: synthetic DNA
Resolution:
2.50Å
R-factor:
0.247
R-free:
0.290
Authors:
H.Yokoyama,R.Mizutani,Y.Satow
Key ref:
H.Yokoyama
et al.
(2013).
Structure of a double-stranded DNA (6-4) photoproduct in complex with the 64M-5 antibody Fab.
Acta Crystallogr D Biol Crystallogr,
69,
504-512.
PubMed id: 23519658
DOI: 10.1107/S0907444912050007
Structure of a double-stranded DNA (6-4) photoproduct in complex with the 64M-5 antibody Fab.
H.Yokoyama,
R.Mizutani,
Y.Satow.
ABSTRACT
DNA photoproducts with (6-4) pyrimidine-pyrimidone adducts formed by ultraviolet
radiation have been implicated in mutagenesis and cancer. The crystal structure
of double-stranded DNA containing the (6-4) photoproduct in complex with the
anti-(6-4)-photoproduct antibody 64M-5 Fab was determined at 2.5 Å
resolution. The T(6-4)T segment and the 5'-side adjacent adenosine are flipped
out of the duplex and are accommodated in the concave antigen-binding pocket
composed of six complementarity-determining regions (CDRs). A loop comprised of
CDR L1 residues is inserted between the flipped-out T(6-4)T segment and the
complementary DNA. The separation of strands by the insertion of the loop
facilitates extensive and specific recognition of the photoproduct. The DNA
helices flanking the T(6-4)T segment are kinked by 87°. The 64M-5 Fab
recognizes the T(6-4)T segment dissociated from the complementary strand,
indicating that the (6-4) photoproduct can be detected in double-stranded DNA as
well as in single-stranded DNA using the 64M-5 antibody. The structure and
recognition mode of the 64M-5 antibody were compared with those of the DNA (6-4)
photolyase and nucleotide-excision repair protein DDB1-DDB2. These proteins have
distinctive binding-site structures that are appropriate for their functions,
and the flipping out of the photolesion and the kinking of the DNA are common to
mutagenic (6-4) photoproducts recognized by proteins.