From owner-biophys@hgmp.mrc.ac.uk Sun Apr 29 19:28:59 2001 Return-Path: Received: from localhost (localhost [127.0.0.1]) by mercury.hgmp.mrc.ac.uk (Postfix) with ESMTP id 3549E17A91 for ; Sun, 29 Apr 2001 19:28:58 +0100 (BST) Received: from localhost (localhost [127.0.0.1]) by mercury.hgmp.mrc.ac.uk (Postfix) with ESMTP id A58C317AD3; Sun, 29 Apr 2001 19:28:54 +0100 (BST) Received: from niobium.hgmp.mrc.ac.uk (niobium [193.62.192.41]) by mercury.hgmp.mrc.ac.uk (Postfix) with ESMTP id 8DFB217A91; Sun, 29 Apr 2001 19:28:51 +0100 (BST) Received: (from news@localhost) by niobium.hgmp.mrc.ac.uk (8.9.3+Sun/8.8.8) id TAA12375; Sun, 29 Apr 2001 19:28:50 +0100 (BST) X-Authentication-Warning: niobium.hgmp.mrc.ac.uk: news set sender to using -f Message-ID: <3AEC5FEC.CFCAB612@mail.ncifcrf.gov> From: "Dr. Artem Evdokimov" Organization: NCI-FCRDC PSB-MCL Protein Engineering X-Mailer: Mozilla 4.74 [en] (Windows NT 5.0; U) X-Accept-Language: en,uk,ru MIME-Version: 1.0 X-Newsgroups: bionet.biophysics,bionet.general,bionet.molec-model Subject: Re: Salt bridges References: <9ch1lu$4j6$1@ulysses.noc.ntua.gr> Content-Type: text/plain; charset=us-ascii Content-Transfer-Encoding: 7bit Lines: 32 Date: Sun, 29 Apr 2001 14:39:40 -0400 To: bioforum@hgmp.mrc.ac.uk, biophys@hgmp.mrc.ac.uk, molmodel@hgmp.mrc.ac.uk Sender: owner-biophys@hgmp.mrc.ac.uk Precedence: bulk You could try scanning calorimetry in D2O and D2O/H2O mixtures, however interpreting these results would be quite tricky. NMR might work, but you most likely won't be able to observe the protons of the salt bridge directly (high exchange) more likely to observe the changes in other nuclei of the residues involved in the bridge(s), especially if you play with pH and other variables. If the protein crystallizes then your best bet is still doing the structure - it is not as difficult as it may seem (with a known starting structure, provided that crystals of the mutant behave well, it only takes 1-2 days to obtain the structure of the mutant). Artem Mavrommatis Kostas wrote: > > Hi everybody, > does anybody knows if there is an experimental method for identifying the > formation of a salt bridge, apart from structural studies? > I have some mutants of a protein that are supposed to form different number > of salt bridges and I want to verify this. > Is there a way to do this by using chaotropic salts or DSC? or something > else? > > I thank you in advance. -- |Dr. Artem Evdokimov Protein Engineering | | NCI-Frederick Tel. (301)846-5401 | | FAX (301)846-7148 | | eudokima@mail.ncifcrf.gov | | http://www.ncifcrf.gov/plague | .