首页 | 本学科首页   官方微博 | 高级检索  
   检索      


Hydrogen exchange kinetics of surface peptide amides in bovine pancreatic trypsin inhibitor
Authors:E Tüchsen  C Woodward
Institution:1. Department of Pharmaceutical Sciences, University of Michigan, Ann Arbor, MI 48109, United States;2. Biointerfaces Institute, University of Michigan, Ann Arbor, MI 48109, United States;3. Department of Chemistry, University of Michigan, Ann Arbor, MI 48109, United States;4. Department of Chemistry, University of Kansas, Lawrence, KS 66045, United States;5. Department of Pharmaceutical Chemistry, University of Kansas, Lawrence, KS 66045, United States;6. Protein Metrics Inc., San Carlos, CA 94070, United States;7. MS Bioworks, Ann Arbor, MI 48108, United States;8. Promega Corporation, Madison, WI 53713, United States;9. Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48109, United States;1. Department of Chemistry and Biochemistry, University of California Santa Cruz, Santa Cruz, CA 95064, United States;2. Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, United States;3. Department of Chemistry, East Carolina University, Greenville, NC 27858, United States;4. Department of Pharmaceutical Chemistry, School of Pharmacy, University of California San Francisco, San Francisco, CA 94158, United States;5. National Center for Advancing Translational Sciences, National Institutes of Health, 9800 Medical Center Drive, Rockville, MD 20850, United States;6. Department of Chemistry and California Institute for Quantitative Biosciences (QB3), University of California Berkeley, Berkeley, CA 94720, United States;7. Cornell University, Northeastern Collaborative Access Team, Argonne National Laboratory, Argonne, IL, United States
Abstract:The acid and base catalytic rate constants, kH, obs and kOH, obs and the pH at the minimum rate, pHmin, of 25 rapidly exchanging protons in bovine pancreatic trypsin inhibitor have been determined. Here we report the labeling procedure giving 1H nuclear magnetic resonance spectral resolution of seven additional rapidly exchanging NH protons and the pH dependence of their chemical shifts. Values of kH,obs kOH,obs and pHmin are given for Ala16, Gly28 and Arg53 NH groups, the only backbone amide protons with static accessibility of more than zero in the crystal structure not previously reports, and for Gly56 NH, buried at the C terminus of an alpha-helix. All four protons reported here have pH min greater than or equal to 3. Conclusions of the previous study predict that peptide protons with pHmin higher than those of model compounds have greater static accessibility of the peptide O than of the peptide N atom. The locations in the crystal structure of the four NH groups whose exchange rates are reported here are in qualitative agreement with these predictions. The ionic strength dependence of Ala16 at pH 5.5 shows a sharp increase in the exchange rate with decreasing salt concentration, as expected for base-catalyzed exchange in a positive electrostatic field.
Keywords:
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号