Jay P. Morgenstern
Merck & Co.
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Featured researches published by Jay P. Morgenstern.
Gene | 1992
Irwin J. Griffith; Sandra J. Craig; Joanne Pollock; Xu-Bo Yu; Jay P. Morgenstern; Bruce L. Rogers
The genes encoding chain 1 (Ch1) and chain 2 (Ch2) of the major allergen of the domestic cat, Felis domesticus I, have been analyzed by genomic cloning and by polymerase chain reaction (PCR). Ch1 has two potential leader sequences, designated A and B. Analysis of a genomic clone encoding Ch1 demonstrated that one structural gene contains sequences corresponding to both leaders, which utilize different Met start codons. PCR analysis showed that genes encoding Ch1 and Ch2 are co-expressed in both the salivary glands and the skin, and that leader sequence A of Ch1 is utilized preferentially in both tissues. Ch2 was shown to have two dominant forms that are differentially expressed in the aforementioned tissues. The long form (Ch2L), composed of 92 amino acids (aa), is preferentially expressed in the salivary glands, while the short form (Ch2S), composed of 90 aa, is preferentially expressed in the skin. There is minor sequence polymorphism in both forms of Ch2. A genomic clone for Ch2 only contained sequences for Ch2S, suggesting that Ch2L is encoded by an exon not contained within this genomic clone.
Molecular Immunology | 1993
Bruce Rogers; Jay P. Morgenstern; Richard D. Garman; Julian F. Bond; Kuo Mei-Chang
This study describes the properties of the two recombinantly expressed polypeptide chains of Fel d I, the major allergen produced by the domestic cat (Felis domesticus). An inframe linker encoding polyhistidine has been added to the 5 ends of the Fel d I chains 1 and 2 cDNAs to facilitate purification using Ni2+ ion affinity chromatography. This method provides high yields in a single step of rchain 1 and rchain 2 of Fel d I with a > 90% level of purity. Polymerase chain reaction (PCR) methods were used to introduce a thrombin cleavage site (LVPR decreases GS) at the N-terminus of both chains. Thrombin cleavage of rchain 1 and rchain 2 followed by HPLC purification of the cleavage products allowed the isolation of each recombinant chain with only two additional residuals (GS) at the N-terminus of the native sequence. Amino acid sequencing analysis of the N-terminus and mass spectrometry of these polypeptides demonstrated that they are highly pure and full-length. Direct ELISA assays showed that IgE from cat-allergic patients binds to both rchain 1 and rchain 2 of Fel d I, demonstrating that both these chains contribute to the allergenicity of this heterodimeric protein. An examination of the reactivity of T cells derived from cat-allergic patients revealed that both polypeptide chains contribute to the T cell response to this allergen. Consequently, it is concluded that the immunological response to Fel d I is composed of a reaction at both the B and T cell level to each of the two chains that constitute the native allergen.
Molecular Immunology | 1994
Bruce L. Rogers; Julian F. Bond; Sandra J. Craig; Anneliese K. Nault; Debra B. Segal; Jay P. Morgenstern; Chen Meei-Song; Christine B. Bizinkauskas; Catherine M. Counsell; Annette M. Lussier; Thomas Luby; Kuo Mei-Chang; Thomas J. Briner; Richard D. Garman
The complete primary structure of Fel d I2 has been determined and shown to be comprised of two separate polypeptide chains (designated chain 1 and 2). Overlapping peptides covering the entire sequence of both chains of Fel d I have been used to map the major areas of human T cell reactivity. The present study describes three non-contiguous T cell reactive regions of < 30 aa in length that were assembled in all six possible configurations using PCR and recombinant DNA methods. These six recombinant proteins comprised of defined non-contiguous T cell epitope regions artificially combined into single polypeptide chains have been expressed in E. coli, highly purified, and examined for their ability to bind to human cat-allergic IgE and for human T cell reactivity. Several of these recombined T cell epitope-containing polypeptides exhibit markedly reduced IgE binding as compared to the native Fel d I. Importantly, the human T cell reactivity to individual T cell epitope-containing regions is maintained even though each was placed in an unnatural position as compared to the native molecule. In addition, T cell responses to potential junctional epitopes were not detected. It was also demonstrated in mice that s.c. injection of T cell epitope-containing polypeptides inhibits the T cell response to the individual peptides upon subsequent challenge in vitro. Thus, these recombined T cell epitope-containing polypeptides, which harbor multiple T cell reactive regions but have significantly reduced reactivity with allergic human IgE, constitute a novel potential approach for desensitization to important allergens.
Archive | 1996
Bruce L. Rogers; Julian F. Bond; Jay P. Morgenstern; Catherine M. Counsell; Irwin J. Griffith
Pollen from short ragweed (Ambrosia artemisiifolia) is the source of one of North America’s most important allergens (King, 1976). Ambrosia artemisiifolia is a widespread weed of the Compositae family, which is comprised of several related species (King and Norman, 1986). Although the pollinating season for ragweed varies depending on the geographical location, it is generally from midsummer to late autumn in the eastern and central United States. Approximately 10% of the U.S. population is allergic to ragweed pollen, making this allergen source highly significant in terms of clinical disease.
Journal of Immunology | 1991
Bruce L. Rogers; Jay P. Morgenstern; Irwin J. Griffith; Xu-Bo Yu; C. M. Counsell; A. W. Brauer; Te Piao King; R. D. Garman; Mei-Chang Kuo
Archive | 1991
Bruce L. Rogers; Jay P. Morgenstern; Julian F. Bond; Richard D. Garman; Julia L. Greenstein; Mei-Chang Kuo; Malcolm Morville
Archive | 1993
Jay P. Morgenstern; Andrzej Konieczny; Christine B. Bizinkauskas; Andrew W Brauer
Archive | 1994
Bruce L. Rogers; Jay P. Morgenstern; Julian F. Bond; Richard D. Garman; Mei-chang Kuo; Malcolm Morville; Julia L. Greenstein
Archive | 1994
Richard D. Garman; Mei-Chang Kuo; Julia L. Greenstein; Bruce L. Rogers; Jay P. Morgenstern; Julian F. Bond; Malcolm Morville
Archive | 1993
Jay P. Morgenstern; Andrzej Konieczny; Christine B. Bizinkauskas; Andrew W Brauer