Literature DB >> 8880877

Rational design for the development of epidermal growth factor receptor antagonists.

E J van Zoelen1, A E Lenferink, R H Kramer, M L van de Poll.   

Abstract

Epidermal growth factor (EGF) and transforming growth factor-alpha (TGF alpha) bind with similar high affinity to the human EGF receptor. Using a domain-exchange strategy we have shown that the C-terminal linear region of these molecules is involved in high affinity receptor binding. By further single amino acid substitution in this linear C-terminal region, a putative interaction site of these ligands with their receptor has been identified. This identification of a receptor binding domain in EGF/TGF alpha provides an important initial step in the development of EGF receptor antagonists with significant clinical potential.

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Year:  1996        PMID: 8880877     DOI: 10.1016/S0344-0338(96)80098-7

Source DB:  PubMed          Journal:  Pathol Res Pract        ISSN: 0344-0338            Impact factor:   3.250


  2 in total

1.  Potency and stability of C terminal truncated human epidermal growth factor.

Authors:  D P Calnan; A Fagbemi; J Berlanga-Acosta; T Marchbank; T Sizer; K Lakhoo; A D Edwards; R J Playford
Journal:  Gut       Date:  2000-11       Impact factor: 23.059

2.  Modulation of key signal transduction molecules by a novel peptide combination effective for the treatment of gastrointestinal carcinomas.

Authors:  Anu T Singh; Manu Jaggi; Sudhanand Prasad; Sarjana Dutt; Gurvinder Singh; Kakali Datta; Praveen Rajendran; Vinod K Sanna; Rama Mukherjee; Anand C Burman
Journal:  Invest New Drugs       Date:  2008-03-06       Impact factor: 3.850

  2 in total

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