Published 1986 | Version v1
Report Open

Carboxyl group reactivity in actin

Description

While earlier work showed that the carboxyl groups of proteins could be quantitatively coupled to amino groups at pH 4.75 in the presence of EDC and a denaturing agent, the work presented here indicates that under milder conditions the modification of sidechain carboxyls is limited and somewhat specific. Most of the incorporated glycine ethyl ester (GEE) is apparently bound to five carboxyls. The total GEE incorporated was 3 to 4 moles/mole of protein as measured by an increase in Gly upon acid hydrolysis and amino acid analysis, as well as total radioactivity. 3.55 residues were found in peptides, 2.75 bound to residues 1 to 4, and 0.8 bound to Gly-100. 9 refs., 2 figs., 2 tabs

Availability note (English)

MF available from INIS under the Report Number; Available from NTIS, PC A02/MF A01; 1 as DE87003197.

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Additional details

Publishing Information

Imprint Pagination
9 p.
Report number
BNL--38848

Conference

Title
6. international conference on methods in protein sequence analysis.
Dates
1-1 Aug 1986.
Place
Seattle, WA (USA).

INIS

Country of Publication
United States
Country of Input or Organization
United States
INIS RN
18064886
Subject category
S60: APPLIED LIFE SCIENCES;
Resource subtype / Literary indicator
Conference
Descriptors DEI
ACTIN; CARBON 14 COMPOUNDS; GEL PERMEATION CHROMATOGRAPHY; HYDROLYSIS; LIQUID COLUMN CHROMATOGRAPHY; PEPTIDES; PROTEIN STRUCTURE; STRUCTURE-ACTIVITY RELATIONSHI; TRACER TECHNIQUES
Descriptors DEC
CARBON COMPOUNDS; CHEMICAL REACTIONS; CHROMATOGRAPHY; DECOMPOSITION; ISOTOPE APPLICATIONS; ORGANIC COMPOUNDS; PROTEINS; SEPARATION PROCESSES; SOLVOLYSIS

Optional Information

Notes
Portions of this document are illegible in microfiche products.
Secondary number(s)
CONF-8608145--1.