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Griffey, R. H.; Greig, M. J.; Sasmor, H.; Cummins, L. L.; Manalili, S. L.; Gaus, H. J.; In NATO ASI series, 1998, "New Methods for the Study of Molecular Aggregates", K. G. Standing, Ed., pp 117-133, Kluwer: Dordrecht.
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Adamiak, D. A.; Milecki, J.; Popenda, M.; Adamiak, R. W.; Dauter, Z.; Rypniewski, W. R.; Nurl. Acids Res. 1997, 25, 4599-4607.
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Dauter, Z.5
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12
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0029812492
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(a) Miyaguchi, H.; Narita, H.; Sakamoto, K.; Yokoyama, S.; Nucl. Acids Res. 1996, 24, 3700-3706.
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(b) Fourmy, D.; Recht, M. I.; Blanchard, S. C.; Puglisi, J. D.; Science 1996, 274, 1367-1371.
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16
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1842388479
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D values are ∼0.2 μM: (a) Recht, M. I.; Fourmy, D.; Blanchard, S. C.; Dahlquist, K. D.; Puglisi, J. D.; J. Mol. Biol. 1996, 262, 421-436. (b) Wong, C. H.; Hendrix, M.; Priestley, E. S.; Greenberg, W. A.; Chem. Biol. 1998, 5, 397-406. (c) Wang, Y.; Hamasaki, Y.; Rando, R. R.; Biochemistry, 1997, 36, 768-779.
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Puglisi, J.D.5
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17
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0032126750
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D values are ∼0.2 μM: (a) Recht, M. I.; Fourmy, D.; Blanchard, S. C.; Dahlquist, K. D.; Puglisi, J. D.; J. Mol. Biol. 1996, 262, 421-436. (b) Wong, C. H.; Hendrix, M.; Priestley, E. S.; Greenberg, W. A.; Chem. Biol. 1998, 5, 397-406. (c) Wang, Y.; Hamasaki, Y.; Rando, R. R.; Biochemistry, 1997, 36, 768-779.
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Hendrix, M.2
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Greenberg, W.A.4
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18
-
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0031051477
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-
D values are ∼0.2 μM: (a) Recht, M. I.; Fourmy, D.; Blanchard, S. C.; Dahlquist, K. D.; Puglisi, J. D.; J. Mol. Biol. 1996, 262, 421-436. (b) Wong, C. H.; Hendrix, M.; Priestley, E. S.; Greenberg, W. A.; Chem. Biol. 1998, 5, 397-406. (c) Wang, Y.; Hamasaki, Y.; Rando, R. R.; Biochemistry, 1997, 36, 768-779.
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Wang, Y.1
Hamasaki, Y.2
Rando, R.R.3
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19
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-
84920313164
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-
note
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pp to minimize the intensity of the parent ion and to generate the highest abundance of fragment ions. A total of 128 scans were summed over m/z 700-2700 following trapping for 100 ms.
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-
-
-
20
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-
44049123270
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(a) McLuckey, S. A.; Van Berkel, G. J.; Glish, G. L.; J. Am. Soc. Mass Spectrom. 1992, 3, 60-70.
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, vol.3
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McLuckey, S.A.1
Van Berkel, G.J.2
Glish, G.L.3
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22
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0344139265
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in press
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The libraries have been synthesized from a mixture of charged and aromatic functional groups, and are described as libraries 25 and 23 in: An, H.; Haly, B. D.; Cook, P. D.; Bioorg. Med. Chem. Lett. 1998, in press.
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(1998)
Bioorg. Med. Chem. Lett.
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An, H.1
Haly, B.D.2
Cook, P.D.3
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