Direct probing of zwitterion formation in unsolvated peptides.

نویسندگان

  • Rodolphe Antoine
  • Michel Broyer
  • Philippe Dugourd
  • Gary Breaux
  • Frederick C Hagemeister
  • David Pippen
  • Robert R Hudgins
  • Martin F Jarrold
چکیده

Molecular beam electric deflection measurements have been used to determine electric susceptibilities for small unsolvated alanine-based peptides. The electric susceptibility provides information about the charge distribution within the peptide and can be used to distinguish between zwitterionic and canonical forms. Measured electric susceptibilities for WAn peptides (n = 1-5) are similar to those for capped Ac-WAn-NH2 peptides (which cannot form zwitterions). Susceptibilities calculated using a simulated tempering-based approach are substantially larger for the zwitterionic form than for the canonical form. The measured susceptibilities are in good agreement with those calculated for the canonical form. For the larger peptides, the lowest potential energy structure found in the simulations is hairpin-like, while the lowest free energy structure found at room temperature is extended. The zwitterionic form is constrained by intramolecular interactions which make it entropically unfavorable.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Probing helix formation in unsolvated peptides.

Ion mobility measurements have been used to examine helix formation in unsolvated glycine-based peptides containing three alanine residues. Nine sequence isomers of Ac-[12G3A]K+H(+) were studied (Ac = acetyl, G = glycine, A = alanine, and K = lysine). The amount of helix present for each peptide was examined using two metrics, and it is strongly dependent on the proximity and the location of th...

متن کامل

Helices and Sheets in vacuow

The structures and properties of unsolvated peptides large enough to possess secondary structure have been examined by experiments and simulations. Some of the factors that stabilize unsolvated helices and sheets have been identified. The charge, in particular, plays a critical role in stabilizing a-helices and destabilizing b-sheets. Some helices are much more stable in vacuum than in aqueous ...

متن کامل

The energy landscape of unsolvated peptides: helix formation and cold denaturation in Ac-A4G7A4 + H+.

Ion mobility measurements and molecular dynamics simulations were performed for unsolvated A4G7A4 + H+ and Ac-A4G7A4 + H+ (Ac = acetyl, A = alanine, G = glycine) peptides. As expected, A4G7A4 + H+ adopts a globular conformation (a compact, random-looking, three-dimensional structure) over the entire temperature range examined (100-410 K). Ac-A4G7A4 + H+ on the other hand is designed to have a f...

متن کامل

Peptides and proteins in the vapor phase.

This article provides a review of recent studies of the properties of unsolvated (and partially solvated) peptides and proteins. The methods used to produce vapor-phase peptide and protein ions are described along with some of the techniques used to study them, such as H/D exchange, blackbody infrared radiative dissociation, and ion mobility measurements. Studies of unsolvated peptides and prot...

متن کامل

The initial steps in the hydration of unsolvated peptides: water molecule adsorption on alanine-based helices and globules.

Equilibrium constants for the adsorption of the first water molecule onto a variety of unsolvated alanine-based peptides have been measured and Delta H degrees and DeltaS degrees have been determined. The studies were designed to examine the effects of conformation, charge, and composition on the propensity for peptides to bind water. In general, water adsorption occurs significantly more readi...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Journal of the American Chemical Society

دوره 125 30  شماره 

صفحات  -

تاریخ انتشار 2003