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Featured researches published by V. Viswanatha.


Biochemical and Biophysical Research Communications | 1980

The tyrosine ring of oxytocin undergoes hindered rotation when the hormone is bound to neurophysin.

Michael Blumenstein; Victor J. Hruby; V. Viswanatha

Abstract Tyrosine specifically enriched with 13C in the meta positions has been chemically synthesized and incorporated into oxytocin via solid phase peptide synthesis. The 13C nmr spectrum of a 1:1 mixture of the enriched hormone complexed to neurophysin was obtained. The spectrum consisted of three peaks. The two outer peaks, representing 85% of the total intensity, were of equal area, had shifts of −0.9 and +2.4 parts per million relative to the free peak, and each had a linewidth of 100 hz at 20°C, with increasing linewidths at higher temperatures. These two peaks arise from a binding mode in which tyrosine ring rotation is hindered by interaction with neurophysin. The rotation rate at 20°C is 130s−1, and at 42°C is 900s−1. The central peak occurred at the position of the resonance due to free hormone, had a temperature independent linewidth of 30–40 hz, and represented about 15% of the total intensity. We believe this peak is due to a binding mode in which tyrosine ring rotation is rapid, 104–108s−1.


Journal of Chromatographic Science | 1978

Reverse Phase High Pressure Liquid Chromatography for the Separation of Peptide Hormone Diastereoisomers

Brent Larsent; V. Viswanatha; Sai Y. Chang; Victor J. Hruby


Journal of the American Chemical Society | 1979

Active site studies of neurohypophyseal hormones: comparison of oxytocin and arginine-vasopressin with analogs containing 4-D-glutamine

Victor J. Hruby; Henry I. Mosberg; V. Viswanatha


Journal of the American Chemical Society | 1982

Biosynthesis of the antitumor antibiotic naphthyridinomycin

Milton J. Zmijewski; Marcia Mikolajczak; V. Viswanatha; Victor J. Hruby


International Journal of Peptide and Protein Research | 2009

Pharmacological, conformational and dynamic properties of cycloleucine‐2 analogues of oxytocin and [1‐penicillamine]oxytocin

Victor J. Hruby; Todd W. Rockway; V. Viswanatha; W. Y. Chan


Journal of Organic Chemistry | 1980

Conversion of L-tyrosine to L-phenylalanine. Preparation of L-[3′,5′-13C2]phenylalanine

V. Viswanatha; Victor J. Hruby


Journal of Organic Chemistry | 1979

Synthesis of [3′,5′-13C2]tyrosine and its use in the synthesis of specifically labeled tyrosine analogues of oxytocin and arginine-vasopressin and their 2-D-tyrosine diastereoisomers

V. Viswanatha; Victor J. Hruby


Biochemistry | 1979

Investigation of the interactions of oxytocin with neurophysins at low pH using carbon-13 nuclear magnetic resonance and carbon-13-labeled hormones.

Michael Blumenstein; Victor J. Hruby; V. Viswanatha


Biochemistry | 1984

Carbon-13 chemical shifts on oxytocin as a consequence of its interaction with neurophysins

Michael Blumenstein; Victor J. Hruby; V. Viswanatha; Dhirendra N. Chaturvedi


Journal of Labelled Compounds and Radiopharmaceuticals | 1980

Synthesis of S-benzyl-DL-[1-13C]cysteine and its incorporation into oxytocin and [8-arginlne]vasopressin and related compounds by total synthesis. Separation of diastekeoisomers by partition chromatography and HPLC†

Victor J. Hruby; V. Viswanatha; Young C. S. Yang

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