scispace - formally typeset
H

Hernando Curtidor

Researcher at Del Rosario University

Publications -  105
Citations -  2036

Hernando Curtidor is an academic researcher from Del Rosario University. The author has contributed to research in topics: Plasmodium falciparum & Peptide sequence. The author has an hindex of 22, co-authored 105 publications receiving 1884 citations. Previous affiliations of Hernando Curtidor include Universidad de La Sabana & National University of Colombia.

Papers
More filters
Journal ArticleDOI

Identification of Plasmodium falciparum MSP-1 peptides able to bind to human red blood cells.

TL;DR: Results show that peptides based on conserved and dimorphic regions of MSP‐1, interact with human red blood cells (RBCs), and showed that the RBC receptors are not sialic acid dependent and appear to be proteic in nature.
Journal ArticleDOI

Plasmodium falciparum EBA-175 kDa protein peptides which bind to human red blood cells

TL;DR: Using synthetic peptides and specific receptor-ligand interaction methodology, 6 high-activity binding sequences from the EBA-175 CAMP strain are identified and several of these peptides are located in regions recognized by protective immune clusters of merozoites eluted antibodies.
Journal ArticleDOI

Intimate molecular interactions of P. falciparum merozoite proteins involved in invasion of red blood cells and their implications for vaccine design.

TL;DR: The results show that Merozoite Surface Protein-9 (MSP-9) or Acid Basic Repeat Antigen (ABRA) 3679 is superior to other MSPs tested on the basis of its ability to bind to EMTs.
Journal ArticleDOI

Plasmodium vivax in vitro continuous culture: the spoke in the wheel

TL;DR: The most relevant aspects regarding P. vivax in vitroculture and host cell characteristics have been analysed in this review to explain possible reasons why the species’ continuous in vitro culture is so difficult to standardize.
Journal ArticleDOI

Plasmodium vivax MSP-1 peptides have high specific binding activity to human reticulocytes.

TL;DR: Interestingly, some high activity binding peptides (HABPs) are located close to the hypothesised 42 and 19kDa fragment cleavage sites for this protein, suggesting that these sequences have an important role in target cell attachment and invasion process by Pv-MSP-1.