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* Residue conservation analysis
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J Mol Biol
243:283-297
(1994)
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PubMed id:
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Preparation, characterization and crystallization of an antibody Fab fragment that recognizes RNA. Crystal structures of native Fab and three Fab-mononucleotide complexes.
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P.R.Pokkuluri,
F.Bouthillier,
Y.Li,
A.Kuderova,
J.Lee,
M.Cygler.
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ABSTRACT
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Fab fragments from Jel 103, an antibody which specifically binds to
single-stranded poly(rl), were prepared by papain digestion, separated into
eight isoforms and characterized by mass spectrometry. One of the purified
isoforms yielded crystals suitable for structural studies by X-ray diffraction
and its crystal structure was determined to 2.4 A resolution. Soaking the
crystals in solutions containing either of the mononucleotides
inosine-5'-diphosphate, guanosine-5'-diphosphate or
deoxyinosine-5'-monophosphate resulted in binding of the nucleotide in a single
binding site. However, adenosine-5'-diphosphate does not bind to this antibody.
The recognition of the base is achieved through hydrogen bonds to the C6
carbonyl oxygen and the imino NH group of the purine in a pattern similar to
that of the base-base interactions in a double-stranded nucleic acid. Additional
binding energy is provided by stacking of the base and the Tyr32L side-chain and
by interaction of the alpha-phosphate with the antibody in an anionic binding
site. Most of the side-chains interacting with the nucleotide come from the
light chain. Surprisingly, this antibody shares the VL sequence with another
nucleic acid-binding antibody, BV04-1. The latter binds to a single stranded DNA
with a high preference for thymine bases. The structures of the unliganded and
complexed Jel 103 Fab are compared to those of BV-04-1 Fab and while they show
similarity in recognition of the base of the immunodominant nucleotide, their 5'
phosphates occupy different positions, suggesting different orientation of the
nucleic acid bound to these two antibodies. Differences in the conformations of
the L1 loops between the two Fabs have been noted.
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Literature references that cite this PDB file's key reference
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PubMed id
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Reference
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S.Chang,
L.Yang,
Y.M.Moon,
Y.G.Cho,
S.Y.Min,
T.J.Kim,
Y.J.Kim,
W.Patrick,
H.Y.Kim,
and
C.Mohan
(2009).
Anti-nuclear antibody reactivity in lupus may be partly hard-wired into the primary B-cell repertoire.
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Mol Immunol,
46,
3420-3426.
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Z.Liang,
S.Chang,
M.S.Youn,
and
C.Mohan
(2009).
Molecular hallmarks of anti-chromatin antibodies associated with the lupus susceptibility locus, Sle1.
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Mol Immunol,
46,
2671-2681.
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J.D.Ye,
V.Tereshko,
J.K.Frederiksen,
A.Koide,
F.A.Fellouse,
S.S.Sidhu,
S.Koide,
A.A.Kossiakoff,
and
J.A.Piccirilli
(2008).
Synthetic antibodies for specific recognition and crystallization of structured RNA.
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Proc Natl Acad Sci U S A,
105,
82-87.
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PDB code:
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M.J.Bobeck,
and
G.D.Glick
(2007).
Role of conformational dynamics in sequence-specific autoantibody*ssDNA recognition.
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Biopolymers,
85,
481-489.
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P.Scheerer,
A.Kramer,
L.Otte,
M.Seifert,
H.Wessner,
C.Scholz,
N.Krauss,
J.Schneider-Mergener,
and
W.Höhne
(2007).
Structure of an anti-cholera toxin antibody Fab in complex with an epitope-derived D-peptide: a case of polyspecific recognition.
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J Mol Recognit,
20,
263-274.
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PDB code:
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M.J.Clément,
A.Fortuné,
A.Phalipon,
V.Marcel-Peyre,
C.Simenel,
A.Imberty,
M.Delepierre,
and
L.A.Mulard
(2006).
Toward a better understanding of the basis of the molecular mimicry of polysaccharide antigens by peptides: the example of Shigella flexneri 5a.
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J Biol Chem,
281,
2317-2332.
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E.W.Debler,
S.Ito,
F.P.Seebeck,
A.Heine,
D.Hilvert,
and
I.A.Wilson
(2005).
Structural origins of efficient proton abstraction from carbon by a catalytic antibody.
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Proc Natl Acad Sci U S A,
102,
4984-4989.
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PDB codes:
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Z.Liang,
C.Xie,
C.Chen,
D.Kreska,
K.Hsu,
L.Li,
X.J.Zhou,
and
C.Mohan
(2004).
Pathogenic profiles and molecular signatures of antinuclear autoantibodies rescued from NZM2410 lupus mice.
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J Exp Med,
199,
381-398.
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R.Kuroki,
M.Hirose,
Y.Kato,
M.D.Feese,
T.Tamada,
H.Shigematsu,
H.Watarai,
Y.Maeda,
T.Tahara,
T.Kato,
and
H.Miyazaki
(2002).
Crystallization of the functional domain of human thrombopoietin using an antigen-binding fragment derived from neutralizing monoclonal antibody.
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Acta Crystallogr D Biol Crystallogr,
58,
856-858.
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T.Torizawa,
N.Yamamoto,
T.Suzuki,
K.Nobuoka,
Y.Komatsu,
H.Morioka,
O.Nikaido,
E.Ohtsuka,
K.Kato,
and
I.Shimada
(2000).
DNA binding mode of the Fab fragment of a monoclonal antibody specific for cyclobutane pyrimidine dimer.
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Nucleic Acids Res,
28,
944-951.
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H.F.Becker,
Y.Corda,
M.B.Mathews,
J.L.Fourrey,
and
H.Grosjean
(1999).
Inosine and N1-methylinosine within a synthetic oligomer mimicking the anticodon loop of human tRNA(Ala) are major epitopes for anti-PL-12 myositis autoantibodies.
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RNA,
5,
865-875.
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N.Kessler,
D.Perl-Treves,
L.Addadi,
and
M.Eisenstein
(1999).
Structural and chemical complementarity between antibodies and the crystal surfaces they recognize.
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Proteins,
34,
383-394.
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K.Lim,
S.M.Owens,
L.Arnold,
J.C.Sacchettini,
and
D.S.Linthicum
(1998).
Crystal structure of monoclonal 6B5 Fab complexed with phencyclidine.
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J Biol Chem,
273,
28576-28582.
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PDB code:
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B.Gigant,
J.B.Charbonnier,
B.Golinelli-Pimpaneau,
R.R.Zemel,
Z.Eshhar,
B.S.Green,
and
M.Knossow
(1997).
Mechanism of inactivation of a catalytic antibody by p-nitrophenyl esters.
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Eur J Biochem,
246,
471-476.
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K.Rajagopalan,
G.Pavlinkova,
S.Levy,
P.R.Pokkuluri,
M.Schiffer,
B.E.Haley,
and
H.Kohler
(1996).
Novel unconventional binding site in the variable region of immunoglobulins.
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Proc Natl Acad Sci U S A,
93,
6019-6024.
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M.Herrmann,
T.H.Winkler,
H.Fehr,
and
J.R.Kalden
(1995).
Preferential recognition of specific DNA motifs by anti-double-stranded DNA autoantibodies.
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Eur J Immunol,
25,
1897-1904.
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The most recent references are shown first.
Citation data come partly from CiteXplore and partly
from an automated harvesting procedure. Note that this is likely to be
only a partial list as not all journals are covered by
either method. However, we are continually building up the citation data
so more and more references will be included with time.
Where a reference describes a PDB structure, the PDB
code is
shown on the right.
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